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FEATURE ARTICLE
Mechanistic Insights IntoToday’s(andTomorrow’s) Treatments forModerate-to-Severe Psoriasis
Melodie S. Young, Kristine J. Kucera
ABSTRACT: Psoriasis is a chronic immune-mediated dis-ease, and several cytokine pathways in the psoriaticcascade have been identified and investigated asclinical targets for systemic therapy. This review providesan overview of psoriasis, including discussion of clinicalvariants, environmental and genetic risk factors, knowncomorbidities, treatment strategies, and limitations inevaluating disease severity. The manuscript then focuseson addressing how existing biologics target the variouspathways described in the pathogenesis of psoriasis, how
modulating these mechanisms can improve outcomesover time, and how new insights have led to the de-velopment of agents that can target different pathwaysassociatedwith the disease. Overall, biologics that targettumor necrosis factor-! or interleukin-12/23 have estab-lished themselves as effective, well-tolerated treatmentoptions for chronic plaque psoriasis that can quicklyproduce dramatic clinical improvement. Unlike topical,phototherapy, and conventional systemic therapies thatdo not specifically target the underlying pathogenesis ofpsoriasis, biologics have been, and continue to be, de-veloped based on identifying therapeutic targets withinthe immune and inflammatory pathways associatedwith disease development and progression. Recently,interleukin-17A has been identified as a central cytokinedriver in the pathogenesis of psoriasis, and biologic ther-apy targeting this cytokine has recently been approved.Key words: Biologics, Pathogenesis, Psoriasis, Severity,Treatment
Psoriasis is a systemic inflammatory diseasethat affects innate and adaptive immune path-ways (Chiricozzi & Krueger, 2013; Girolomoni,Mrowietz, & Paul, 2012). Although the etiol-ogy of psoriasis is complex and remains largely
unknown, it has become clear over the past several yearsthat psoriasis goes beyond the skin. To effectively target theunderlying disease pathogenesis, drugs are needed that actsystemically on specific molecular components of the im-mune system (Baker et al., 2013; Girolomoni et al., 2012;Sivamani et al., 2013). As understanding of the psoriaticdisease process has improved, several biologic agents havebecome available that inhibit select cytokines associatedwith psoriatic plaque formation (e.g., antitumor necrosisfactor-! [TNF!]Vetanercept, adalimumab, infliximab;interleukin [IL]-12 and IL-23 inhibitorVustekinumab;and IL-17A inhibitorVsecukinumab; Sivamani et al., 2013).Apremilast, a small-molecule inhibitor of phosphodiesterase-4,
2.5 Contact
Hours
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Melodie S. Young, MSN, A/GNP-C, DCNP, Modern DermatologyYABaylor Health Texas Affiliate, Graduate School of Nursing, TheUniversity of Texas at Arlington, Arlington, and Modern ResearchAssociates, Dallas, TX.Kristine J. Kucera, PA-C, MPAS, DHS, Dermatology Center of Frisco,Frisco; UT Southwestern Medical Center, Dallas; and UNT HealthScience Center, Ft. Worth, TX.
Technical assistance with editing and styling of the manuscript forsubmission was provided by Oxford PharmaGenesis, Inc., and wasfunded byNovartis Pharmaceuticals Corporation. The authors werefully responsible for all content and editorial decisions and receivedno financial support or other form of compensation related to thedevelopment of this manuscript. The opinions expressed in the man-uscript are those of the authors, and Novartis Pharmaceuticals hadno influence on the contents.Melodie S. Young is a speaker or consultant for AbbVie, Celgene,Janssen, and Lilly and a clinical investigator for Amgen, Janssen,Novartis, Merck, Celgene, Pfizer, Galderma, and Eli Lilly. Kristine J.Kucera is a speakeror advisor forAbbVie, Actavis, Amgen, Aqua, Bayer,Innocutis, Janssen, Novartis, Promius, and Valeant and a consultantfor Eli Lilly.This is an open-access article distributed under the terms of theCreative Commons Attribution-Non Commercial-No DerivativesLicense 4.0 (CCBY-NC-ND), where it is permissible to downloadand share the work provided it is properly cited. The work cannot bechanged in any way or used commercially.
Correspondence concerning this article should be addressed toMelodie S. Young, MSN, A/GNP-C, DCNP, Modern ResearchAssociates, 9101NCentral Expressway, Suite 170,Dallas, TX75205.E-mail: [email protected]
DOI: 10.1097/JDN.0000000000000186
Copyright © 2016 Dermatology Nurses' Association. Unauthorized reproduction of this article is prohibited.
is also available (Schafer, 2012). In addition, several othersmall molecules are being investigated that inhibit a varietyof kinases (in particular, Janus kinase and protein kinase C;Ortiz-IbaDez, Alsina,&MuDoz-Santos, 2013; Schafer, 2012).Improvements in our understanding of psoriasis have sub-sequently led to the development of newer agents that maytarget themechanism of disease more explicitly. Specifically,IL-17A has been identified as a central cytokine driver in thepathogenesis of psoriasis, and biologic agents targeting thiscytokine are currently in late-stage clinical development(ixekizumab) or have been recently approved (secukinumab;Cai et al., 2011; Chiricozzi et al., 2011; Krueger et al.,2012; Langley et al., 2014; Leonardi et al., 2012).
This article reviews how existing biologics target knownmechanisms of disease in psoriasis and how modulatingthese mechanisms can improve outcomes over time. It alsopresents new insights into the pathophysiology of psori-asis that have led to the development of additional agentsthat target specific pathways associated with the disease.
PSORIASIS: AN OVERVIEWPsoriasis is a common immune-mediated disorder affect-ing an estimated 2%Y3% of the population worldwide(National Psoriasis Foundation [NPF], n.d.-b). Psoriasisis a heterogeneous disease, both in terms of clinical pre-
sentation and risk factors. Table 1 provides a descriptionof the variants of psoriasis, including the frequency andmost common characteristics of each phenotype (Ladizinskiet al., 2013; VillaseDor-Park et al., 2012). By far, the mostcommon variant of psoriasis is plaque psoriasis, which ischaracterized by red, scaly plaques that typically appearon the scalp, elbows, knees, and trunk (Ladizinski et al.,2013). In addition to the skin lesions associated with pso-riasis, an estimated 50% of psoriatic patients have finger-nail involvement, and 35% have toenail involvement(Menter et al., 2008); nail changes may include pitting,oil spots, leukonychia, subungual hyperkeratosis, dystro-phy, and onycholysis (Ladizinski et al., 2013; VillaseDor-Park et al., 2012). Psoriasis is also linked with a numberof comorbidities, including psoriatic arthritis, metabolicsyndrome (clustering of obesity, hypertension, dyslipidemia,and insulin resistance), Type 2 diabetes, and depression. Pso-riatic arthritis is an inflammatory spondyloarthropathy thatis estimated to affect anywhere from 6% to 42% of patientswith psoriasis (Gottlieb et al., 2008); its presentation issomewhat heterogeneous, but characteristic features ofteninclude asymmetric distal oligoarthritis, sausage-like digits(dactylitis), and enthesitis (Gottlieb et al., 2008). In addi-tion to the aforementioned comorbidities, patients withpsoriasis are at increased risk for cardiovascular disease
TABLE 1. Variants of Psoriasis
Variation Frequency Common Signs and Sites of Involvement
Chronicplaque psoriasis
Most common(980% of cases)
& Well-defined, erythematous plaques with adherent silvery scales
& Preferred involvement sites are the scalp, extensor surfaces of the elbowsand knees, and lower trunk
& Chronic course, with periods of remission
Intertriginouspsoriasis
Common & Thin, well-defined, shiny erythematous plaques with minimal scaling
& Preferred involvement sites are the various skin folds including the axillae,behind the ears, inframammary region, and lower trunk
Pustular psoriasis Uncommon & Eruption of sterile pustules; multiple patterns of pustule formation exist
& Preferred involvement sites depend on pattern type
Erythrodermicpsoriasis
Rare & Generalized erythema and scaling; may affect more than 75% of bodysurface area
& Hair loss and nail dystrophy may also be seen; patient may exhibit systemicsymptoms such as fever, chills, and fatigue
& May be acute or chronic
& Potentially life threatening
Guttate psoriasis Rare & Pink, oval (drop-shaped) papules with silvery scaling
& Preferred involvement sites of the trunk and extremities
& May be acute or chronic
& Occurs in younger patients; many progress to chronic plaque psoriasis
& Often develops post-strep throat
Ladizinski et al., 2013; VillaseDor-Park, Wheeler, & Grandinetti, 2012.
30 Journal of the Dermatology Nurses’ Association
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including myocardial infarction, stroke, vascular inflamma-tion, and atherosclerotic disease (Baker et al., 2013; Gelfand&Yeung, 2012; Kimball et al., 2008). Interestingly, it hasbeen observed that patients’ risk for developing many ofthese comorbidities is independent of traditional cardiovas-cular risk factors, especially for thosewithmoderate-to-severedisease. This reinforces the notion that psoriasis is a sys-temic disorder affecting more than just the skin, requir-ing a systemic approach to care (Gelfand & Yeung, 2012;Kimball et al., 2008).
Several genetic factors are strongly linked to psoriasis.Ten chromosomal regions (designated PSORS1YPSORS10)have been identified as being significantly associated withpsoriasis, and many of the genes linked to psoriasis arealso known to regulate specific inflammatory pathways.Overall, it is estimated that individuals with a first-degreerelative affected by psoriasis are four to six times morelikely to develop psoriasis compared with the generalpopulation (Girolomoni et al., 2012). In individuals witha genetic predisposition for psoriasis, many differentenvironmental triggers have been associated with precip-itating the onset or worsening of psoriasis, including in-fection (e.g., streptococcal), skin trauma, use of certainprescription drugs (e.g., lithium, antimalarials, beta blockers,interferon), alcohol consumption, cigarette smoking, stress,excessive exposure to ultraviolet radiation (sunburn), andautoimmune disorders (e.g., vitiligo, celiac disease, thyroiddisease; Mallbris et al., 2005; NPF, 2013; VillaseDor-Parket al., 2012; Wheeler, 2010).
Current consensus is that mild psoriasis can be success-fully treated with topical agents, whereas phototherapy orsystemic or biologic therapy is indicated for moderate-to-severe disease (Baker et al., 2013; Mrowietz et al., 2011).However, psoriasis at any level can have a significantnegative impact on overall quality of life (e.g., even whenonly a small portion of body surface area [BSA] is affected),thereby challenging the label of ‘‘mild’’ disease. Results ofa population-based survey on the burden of psoriasis es-timate that, of the more than 4.5 million adults diagnosedwith psoriasis in the United States, 2.6 million (È60%)have little or no skin involvement, yet more than 1 millionpatients are substantially dissatisfied with their treatment,and roughly half a million Americans report that psoriasisis a major problem in their everyday life (Stern, Nijsten,Feldman, Margolis, & Rolstad, 2004). An estimated 80%(È800,000) of those who report being very dissatisfiedwith treatment and more than 60% (È300,000) of thosewho report psoriasis is a major problem have psoriasiscovering a BSA of less than 10% or 10 palms (Stern et al.,2004). Findings such as these highlight the limitations ofcurrent definitions used for diagnosis of mild versus mod-erate versus severe psoriasis.
European and Australian consensus guidelines for as-sessing the severity of psoriasis rely heavily on the use ofPsoriasis Area and Severity Index (PASI) and DermatologyLifeQuality Index (DLQI) scores, definingmild psoriasis as
PASI e 10 andDLQI e 10 andmoderate-to-severe psoriasisas PASI 9 10 andDLQI 9 10 (Baker et al., 2013; Mrowietzet al., 2011). In addition to the PASI and DLQI requirements,European consensus guidelines also include BSA e 10%asa criterion for mild psoriasis and BSA 9 10% as a criterionfor moderate-to-severe psoriasis (Mrowietz et al., 2011).Although PASI and DLQI are generally considered to berigorous, objective assessments of disease severity, clinicalconsensus from the NPF acknowledges that these classifi-cation instruments are often not practical for use in every-day clinical settings (Pariser et al., 2007). TheNPF consensusstates that disease severity is generally a subjective assess-ment based on the practitioner’s estimation of BSA affectedas well as disease location, lesion thickness, physical symp-toms, and emotional and financial burdens of psoriasis onthe patient’s quality of life (Pariser et al., 2007). In studiesconducted by theNPF, psoriasis is classified asmoderate ifthere is as little as 3% BSA affected (Horn et al., 2007)and as moderate to severe if there is at least 5% BSA in-volvement (Pariser et al., 2007). However, in cases wherepsoriasis affects even small areas in visible or sensitive lo-cations, such as the face, scalp, genitals, nails, and palms orsoles, it is often appropriate to classify psoriasis covering aBSA G 5% as moderate to severe. Other sensitive areas thatshould be considered in psoriasis classification include theeyelids, lips, mouth, and skin folds (NPF, 2008). In addition,regardless of BSA affected, all cases of erythrodermic, pus-tular, and guttate psoriasis should be classified as moderateto severe and treated with systemic therapy and/or photo-therapy (Pariser et al., 2007).
Other factors to consider when determining the sever-ity of psoriasis include the burdens associated with symp-toms of pain, itching, burning, stinging, and bleeding inaffected areas (Baker et al., 2013; Bilac, Ermertcan, Bilac,Deveci, &Horasan, 2009). A recent study that examinedthe etiopathogenesis and burdens of these symptoms foundthat they are frequently associated with reduced quality oflife, affecting mood, sleep, concentration, sexual desire,and appetite (Bilac et al., 2009). In a cross-sectional study,42% of patients with psoriasis reported skin pain (pri-marily of moderate intensity), with sleep being the mostseverely affected function (Ljosaa et al., 2010). Severeitching can be particularly bothersome for patients, andscratching pruritic lesions can lead to excoriation, whichcan worsen or Koebnerize the lesions (Baker et al., 2013).In such cases, psoriasis defined as mild based on BSAshould be reclassified as moderate to severe (Baker et al.,2013). Overall, it is important for dermatology practi-tioners to be aware of the frequency of these symptomsand the negative impact they can have on patients andtheir caregivers and personal relationships when deter-mining psoriasis severity.
Because psoriasis is such a visually apparent disease, itcan cause patients to feel embarrassed, stigmatized,stressed, and depressed. It can also negatively affect bodyimage, personal relationships, intimacy, and employment
VOLUME 8 | NUMBER 1 | JANUARY/FEBRUARY 2016 31
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(Kimball, Jacobson, Weiss, Vreeland, & Wu, 2005;Schmitt & Ford, 2006; Young, 2005). As discussed, thepsychological impact of psoriasis does not always corre-late with disease severity based on BSA involvement (Kimballet al., 2005; Schmitt & Ford, 2006). Even small amountsof psoriasis can greatly affect patients; therefore, it iscritical for practitioners to evaluate each patient for uniqueemotional burdens when recommending treatment strat-egies, recognizing that aggressive therapies may be ap-propriate even with limited disease. Studies have shownthat women and younger patients (G40 years old) may beespecially vulnerable to the social stigma associated withpsoriasis and prone to depression (NPF, 2013; Wheeler,2010). In addition to feeling heightened social stigma,teenage patients may also be sensitive about their need forphysical privacy and independence. They may be reluc-tant to show practitioners the full extent of their disease orto ask a parent for help with medication (e.g., applying atopical treatment to a hard-to-reach area;Wheeler, 2010).
CURRENT TREATMENTS AND FUTURE DIRECTIONSTable 2 presents an overview of available treatments forpsoriasis (Cosentyx [secukinumab] injection prescribinginformation, 2015; Dovonex [calcipotriene] cream pre-scribing information, 2009; Ladizinski et al., prescribinginformation, 2013; NPF prescribing information, n.d.-a;Otezla [apremilast] tablets prescribing information, 2014;Tazorac [tazarotene] cream prescribing information,2011; Vectical [calcitriol] ointment prescribing informa-tion, 2012; Zithranol-RR [anthralin] cream prescribinginformation, 2009). Topical agents, including corticoste-roids, Vitamin D analogs, retinoids, coal tar preparations,and keratolytics, are only recommended for the manage-ment of mild, localized psoriasis (Mrowietz et al., 2011;Pariser et al., 2007). Topical agents cannot effectively con-trol moderate-to-severe psoriasis and do not target the un-derlying disease process (Ladizinski et al., 2013; Mrowietzet al., 2011; Poulin et al., 2012). Patient satisfaction withtopical agents is generally low because of their limitedefficacy and inconvenient administration (Poulin et al., 2012),and topical preparations can be greasy,messy, malodorous,and time-consuming to apply. Certain agents (e.g., coaltars) can also stain skin and clothing (Ladizinski et al., 2013).
To significantly clear skin symptoms and improve pa-tients’ quality of life, it is recommended that patients withmoderate-to-severe psoriasis receive systemic therapy withFood and Drug Administration-approved conventionalagents (e.g., methotrexate, cyclosporine) or biologic agents(e.g., secukinumab, infliximab, adalimumab, etanercept,ustekinumab;Mrowietz et al., 2011). In addition, the newsmall-molecule apremilast should also be considered as itis approved for adults with moderate-to-severe plaque-type psoriasis. The American Academy of Dermatologyreleased a position statement in 2013 stating that ‘‘psoriasispatients with moderate-to-severe psoriasis and, thus, can-didates for systemic therapy, should be placed on the
appropriate therapy from the beginning, i.e., photother-apy, or systemic therapy including biologic therapy’’(American Academy of Dermatology and AAD Associ-ation, 2013). However, despite consensus guidelines issuedby the NPF (Pariser et al., 2007) and expert panels from19European countries (Mrowietz et al., 2011) and acrossAustralia (Baker et al., 2013) recommending the use ofsystemic therapy (possibly in combination with photo-therapy) for the treatment of moderate-to-severe psoria-sis, many dermatology practitioners are still reluctant touse systemic agents as first-line therapy or to switch to sys-temic agents when topical agents are ineffective (Mrowietzet al., 2011). For example, a study by Horn and colleaguesthat surveyed 1657 patients with moderate (BSA of 3%Y10%) or severe (BSA 9 10%) psoriasis from 2003 to 2005found that, among those who were receiving any treat-ment for their psoriasis, most patients with moderatepsoriasis (73%) or severe psoriasis (57%) were receivingonly topical therapy (Horn et al., 2007). More recently,Armstrong, Robertson,Wu, Schupp, and Lebwohl (2013)confirmed that undertreatment of moderate-to-severe pso-riasis was still problematic in surveys conducted through2011. In their survey of 5604 patients with psoriasis orpsoriatic arthritis, these authors found that, in 2011, 23.6%of patients with moderate disease and 9.4% of patients withsevere disease were receiving no treatment, and 29.5% and21.5% (51% combined), respectively, were receiving onlytopical therapy (Armstrong et al., 2013). Furthermore, inthis population with high rates of psoriasis undertreatment,most (52%) of survey respondents were dissatisfied withtheir treatment (Armstrong et al., 2013). More concerningis the limited success of topical treatments beyond milddisease, yet they continue to be the first-line therapy inpractice and have no known therapeutic benefit for man-aging comorbidities such as psoriatic arthritis. In contrast,a 2012 study that evaluated patient satisfaction by class oftherapy for moderate-to-severe psoriasis found that most(63%) of the patients treated with biologics were ‘‘verysatisfied’’ with their treatment (Poulin et al., 2012). Takentogether, the above survey findings highlight the need toincrease education and advocacy about systemic agentsand treatment goals to ensure that patients are appro-priately treated and have realistic expectations regardingthe benefits and risks of such therapy.
The decision to treat patientswith conventional systemicagents or biologics should be based on individualizedneeds, convenience, and safety and efficacy considerationsof a particular agent. For many patients, conventional sys-temic agents are contraindicated, or their use is limitedby common or potentially serious side effects (Table 2).Methotrexate is associated with numerous drug interac-tions and contraindicated in patients with elevated liverenzymes or a history of alcohol abuse, liver disease, orbone marrow hyperplasia. It is also a concern for patientsof reproductive age. Side effects of methotrexate includenausea, vomiting, anorexia, stomatitis, macrocytic anemia,
32 Journal of the Dermatology Nurses’ Association
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TABLE
2.Curren
tTrea
tmen
tsforPsoriasis
Drug
Brand
Name
ModeofA
ctio
nDosa
ge/A
dministra
tion
Contraindicatio
nsSideEffects
Comments
Topicals
Anthralin
Zithranol-R
R(Elorac)
Antip
roliferativ
eand
anti-infla
mmatory
effects
onskin
1.2%
cream
applie
donc
edaily
for5
Y30minutes
and
thenremove
dbywashing
Acuteora
ctiv
ely
infla
medpso
riatic
eruptio
ns
Skin
irrita
tion,
stainingofh
air,
anduna
ffectedskin
Messy,
time
consumingto
apply
andrin
se
Calcipotriene
Dovo
nex(Leo)
Synthetic
Vita
min
D3
analog;slo
wsskin
cellgrowth,fla
ttens
lesio
ns,remove
ssc
ale
0.00
5%cream
or
scalp
solutio
napplie
dto
affectedarea
twicedaily
Hyp
ercalcemia,
Vita
min
Dtoxicity
Skin
irrita
tion,d
ryskin,p
eeling,rash,
derm
atitis,
worsening
ofp
soria
sis
Notforu
seon
theface
Calcitriol
Vectic
al
(Galderm
a)
Naturally
occurring
activ
eform
of
Vita
min
D3;controls
exc
essiveskin
cellproductio
n
Applie
dto
affected
areatw
icedaily;
maximum
dose
,20
0g/w
eek
None
Hyp
ercalciuria
,pruritus,
cha
ngesin
calcium
metabolism
Notforu
seonthe
face,lips,ore
yes
Taza
rotene
Tazo
rac
(Alle
rgan)
Vita
min
Aderiv
ativ
e(retin
oid);thoughtto
slow
skin
growth
Applie
dto
affected
areaoncedaily,
intheeve
ning,to
cove
rlesio
nswith
athin
film
Pregnanc
y(m
ay
cause
fetalh
arm
)Skin
irrita
tion,d
ryskin,susceptib
ility
tosunburn
Canbeuse
don
theface,h
airline,
scalp,a
ndnails
Womenof
childbearin
gage
mustuserelia
ble
birthcontrold
urin
gtreatm
ent
Corticosteroids(e
.g.,
clob
etasol,fluoc
inon
ide,
deso
ximetaso
ne,
hydrocortiso
ne,
flutic
aso
ne,o
thers)
Manybrands/
potencies
Anti-infla
mmatory
propertiesreduce
swellin
gand
redness
oflesio
ns
Varyingstreng
thsand
form
ulatio
nsava
ilable;
gene
rally
applie
donceortwicedaily
None
Skin
thinning,p
igmentatio
nchanges,easy
bruising,
stretchmarks,redness,
dila
tedsurfa
ceblood
vessels,
acne
Notforu
seon
faceoro
ther
sensitiveareasfor
long
perio
ds
Canlose
efficacy
ove
rtim
e;a
brupt
disc
ontin
uatio
ncan
cause
flares
Pulse
dosin
gcan
minim
izeriskof
sideeffects
(continues)
VOLUME 8 | NUMBER 1 | JANUARY/FEBRUARY 2016 33
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TABLE
2.Curren
tTrea
tmen
tsforPsoriasis,Continued
Drug
Brand
Name
ModeofA
ctio
nDos
age/
Administra
tion
Contraindicatio
nsSideEffects
Comments
Salic
ylic
acid
Many
gene
ricOTC
form
ulatio
nsKe
ratolytic
;acts
asasc
ale
lifterto
softenand
remove
pso
riasis
scales
Applie
dasneeded
inconcentratio
ns
upto
3%(creams,
gels,
ointm
ents,
shampoos,so
ap)
None
Skin
irrita
tion
Byremovingsc
ales,
salic
ylic
acid
may
allo
wothertopical
agentsto
better
pene
trate
theskin
Coaltar
Many
gene
ricOTC
form
ulatio
nsCanslo
wskin
growth
andrestore
norm
ala
ppearanc
e
Canbeapplie
ddire
ctly
ora
ddedto
bath
water;gene
rally
leftonskin
forQ
2ho
urs
None
Skin
irrita
tion,redness,
and
dryness;increase
dse
nsitivity
tosunburn
Messy,
strongodor,
stains,ve
rytim
e-consuming
Knowncarcinogenat
highconcentratio
ns
Conv
entiona
lsystemic
therapies
Cyc
losp
orin
eNeoral
(Nova
rtis)
and
others
Immunosuppressant;
slowsgrowth
of
skin
cells
Usually
take
norally
twicedaily
ata
startingdose
of
2.5mg/kg/d
ay
Compromise
dim
munesystem,
activ
ese
rious
infectio
ns,abnorm
al
kidneyfunctio
n,un
controlla
ble
hypertension,c
ancer
orh
istory
ofc
anc
er
(otherthancertain
skin
cancers),se
vere
gout,radiatio
ntherapy,
pregnancy
Decrease
drena
lfunctio
n,hy
pertension,e
leva
ted
cho
lesterola
nd/o
rtriglycerid
es,exc
essive
hairgrowth,tinglingor
burningin
thearm
sorlegs,
skin
sensitivity,swellin
gor
growth
ofg
um
tissue,flu-like
symptoms,upse
tstomach,
fatig
ue,m
usc
leorjointp
ain,
neurologic
symptoms
(e.g.,headache
,tremor)
Increase
driskof
skin
canc
erin
patie
ntstreated
with
PUVA,
methotrexa
te,
oro
ther
immunosuppressants
ManydrugYd
rug
reactio
ns(e.g.,antib
iotic
s,anti-infla
mmatory
agents,antifungals,
calcium
channe
lblocke
rs,a
nticonv
ulsants)
Improve
mentcanoccur
with
in2weeks;c
omplete
resp
onse
maytake
3Y4months
(continues)
34 Journal of the Dermatology Nurses’ Association
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TABLE
2.Curren
tTrea
tmen
tsforPsoriasis,Continued
Drug
Brand
Name
ModeofA
ctio
nDosa
ge/A
dministra
tion
Contraindicatio
nsSideEffects
Comments
Methotrexa
teUsually
sold
as
ageneric
form
ulatio
n
Antim
etabolite;
slowsthe
rate
of
skin
cellgrowth
Usually
take
norally
onc
eaweek;injectable
form
ulatio
nsava
ilable
Alcoholism,a
lcoho
licoro
therc
hronic
liver
dise
ase,immun
odefic
ienc
ysyndromes,womenor
theirpartne
rsplann
ing
pregna
ncy,
activ
epeptic
ulcers,signific
ant
kidne
yorlivera
bno
rmalities,
activ
einfectio
usdise
ase,
hematologic
diso
rders
Nause
a,fatig
ue,
difficulty
sleeping,
lighthe
adedne
ss,
mouth
ulcers,v
omiting,
headache,e
asy
bruisingandbleeding,
feve
r,diarrh
eawith
bloodystools,
chills,
sensitivity
tosunlight,
burningse
nsa
tionin
lesio
ns,hairloss,
liverfibrosis
Regularb
loodtests
neededto
checkforside
effectsontheliver,blood,
orb
onemarro
w
Womenshould
wait
Q4monthsafter
stoppingtreatm
ent
before
becoming
pregnant;menshould
waitQ3monthsbefore
acouple
triesto
conc
eive
Folic
acid
canreducerisk
ofsideeffects
Improve
mentc
anoccur
with
in3Y
6weeks;c
omplete
resp
onse
maytake
6months
Acitretin
Soria
tane
(Stie
fel)
Oralretin
oid;
exa
ct
mecha
nism
unkn
own;
retinoidsregulate
cellbeha
vior,
includingrate
ofskincell
growth
and
shedding
Take
norally
once
daily
with
food
(ava
ilable
in10
-,17
.5-,
and25
-mgdose
s)
Pregna
ncy,
breastfeeding,
seve
relivero
rkidney
dise
ase
,uncontrolle
dhyp
erlipidemia
Hairloss,c
happedlip
s,dry
mouth,
dry
skin
and
eye
s,bleedinggums,
nose
bleeds,se
nsitivity
tosunlight,peeling
fingertips,nailchanges,
cha
ngesin
serum
lipids,depression,
aggressivethoughtsor
thoughtsofself-harm
,he
adache,jointpain,
decrease
dnightv
ision,
eleva
tedlivere
nzymes
Cancause
seve
rebirth
defects;w
omenmust
useQ2birthcontrol
methods,should
not
becomepregnant
for3
yearsafter
disc
ontin
uatio
n
Should
notdonate
bloodfor3
years
afterd
iscontin
uatio
nWomenmustavo
idalcohold
uringtreatm
ent
andfor2
months
afterd
iscontin
uatio
n
Improve
mentm
ay
beslo
w(8Y1
6weeks;
peakeffectafter6
months)
(continues)
VOLUME 8 | NUMBER 1 | JANUARY/FEBRUARY 2016 35
Copyright © 2016 Dermatology Nurses' Association. Unauthorized reproduction of this article is prohibited.
TABLE
2.Curren
tTrea
tmen
tsforPsoriasis,Continued
Drug
Brand
Name
ModeofA
ctio
nDosa
ge/A
dministra
tion
Contraindicatio
nsSideEffects
Comments
Small-molecule
inhibito
rs
Apremila
stOtezla
(Celgene)
Oralsmall-molecule
inhibito
rof
pho
spho
diesterase-4
Titrate
torecommended
dose
of3
0mgtw
icedaily
Knownhyp
ersensitivity
toapremila
stora
nyexc
ipientsin
form
ulatio
n
Diarrh
ea,n
ause
a,
headache
,upper
resp
iratory
tract
infectio
n,v
omiting,
naso
pharyngitis,upper
abdominalp
ain
Inclinicaltria
ls,È30
%of
patie
ntsachieve
dPA
SI75
after1
6weeks
Biologics
Etanercept
Enbrel(Amgen)
Fusio
nprotein
of
TNF!
receptor
extracellular
domain
and
Fcportionof
humanIgG
SCinjectio
n50
mgtw
ice
weeklyfor3
months,then
maintenanc
edose
sonceweeklythereafter
Activ
ese
rious
infectio
n;
history
ofrecurrent
infectio
ns;history
of
heartfailure,m
ultiple
sclerosis,o
rother
demye
linatin
gdise
ase
Dizziness,sore
throat,
cough,stomach
pain,injectio
n-site
reactio
ns,up
per
resp
iratory
infectio
ns,
headache
,rhinitis
Sideeffectsare
generally
mild
and
maydecrease
ove
rtim
e
Inclinicaltria
ls,È49
%of
patie
ntsachieve
dPA
SI75
after3
months
Adalim
umab
Humira
(AbbVie)
Humanrecombinant
IgG
monoclonal
antib
odysp
ecific
forTNF!
SCinjectio
nof8
0mg
onDay1,
then40
mg
eve
ryotherw
eek
startingonDay8
Activ
ese
rious
infectio
n;
history
ofrecurrent
infectio
ns;history
of
heartfailure,m
ultiple
sclerosis,o
rother
demye
linatin
gdise
ase
Upperresp
iratory
tract
infectio
ns,a
bdominal
pain,h
eadache
,rash,
injectio
n-site
reactio
ns,
urin
ary
tractinfectio
ns
Sideeffectsare
generally
mild
and
maydecrease
ove
rtim
e
Inclinicaltria
ls,È70
%ofpatie
nts
achieve
dPA
SI75
after3months
Infliximab
Remicade
(Janssen)
Chimeric
monoclona
lIgG
antib
ody
targetin
gTN
F!
IVinfusio
nof5
mg/kg;
threeinfusio
nsduring
thefirst6weeks,then
onceeve
ry8weeks
Activ
ese
rious
infectio
n;h
istory
ofrecurre
nt
infectio
ns;history
ofh
eartfailure,
multip
lesclerosis,o
rotherd
emye
linating
dise
ase
Infusio
nreactio
ns,
upperresp
iratory
tractinfectio
ns,
headache
,rash,
coug
h,stom
ach
pain
Sideeffe
ctsare
gene
rally
mild
and
maydecrease
ove
rtim
e
Inclinicaltria
ls,È80
%ofp
atie
ntsachieve
dPA
SI75
after1
0weeks
(continues)
36 Journal of the Dermatology Nurses’ Association
Copyright © 2016 Dermatology Nurses' Association. Unauthorized reproduction of this article is prohibited.
phototoxicity, seizures, hepatotoxicity, renal failure, bonemarrow suppression, and pulmonary fibrosis (Aaronson& Lebwohl, 2004; Christophers, Griffiths, Gaitanis, &van de Kerkhof, 2006). In addition, methotrexate hasmore black box warnings than any other therapy forpsoriasis. Cyclosporine is contraindicated in patients withelevated creatinine levels or a history of hypertension, renaldisease, gout, or hyperuricemia. Side effects of cyclosporineinclude nephrotoxicity, hypertension, hyperlipidemia,hypomagnesemia, hyperkalemia, and increased susceptibilityto infection and malignancy (Aaronson & Lebwohl, 2004;Christophers et al., 2006). Retinoids are highly teratogenicand can cause hair loss, dry skin or lips, cheilitis, dermatitis,increased serum lipids and liver enzymes, and osteoporosis(Aaronson & Lebwohl, 2004). Given the long lists of safetyconcerns associated with conventional systemic agents, itis not surprising that a survey of 301 patients with pso-riasis treated at European outpatient clinics found thatmore than 90% of patients had comorbidities that couldpreclude the use of conventional systemics (most commonly,hypertension, abnormal liver enzymes, and hyperlipidemia;Christophers et al., 2006).
The biologic agents approved for the treatment ofmoderate-to-severe psoriasis are all comparably safe andwell tolerated; however, cases of serious infection havebeen observed with these agents, and they may increaserisk of malignancy (Cosentyx [secukinumab] injectionprescribing information, 2015; Enbrel [etanercept] solutionprescribing information, 2015; Humira [adalimumab]injection prescribing information, 2014; Remicade[infliximab] lyophilized concentrate for injection pre-scribing information, 2015; Stelara [ustekinumab] injectionprescribing information, 2014). Recent studies suggestthat the increased risks for infection and malignancy aresmall and may not be statistically significant (Dommaschet al., 2011), but many practitioners choose to avoid usingbiologics in patients with a history of malignancy or withactive or frequent infections. All patients who are candi-dates for biologic therapy should be screened for tuber-culosis, Hepatitis B and C and other serious infections,nonmelanoma skin cancer, and othermalignancies (Ortleb& Levitt, 2012; Sivamani et al., 2013).
Although data are limited on the comparative efficacyof conventional systemics versus biologics (Lee et al., 2012),two randomized controlled trials published to date showedthat adalimumab (Saurat et al., 2008) and infliximab(Barker et al., 2011) were associated with significantlyhigher PASI 75% improvement (PASI 75) responses com-pared with methotrexate. Furthermore, a network meta-analysis of data from 20 randomized controlled trials ofapproved biologic agents for the treatment of moderate-to-severe psoriasis showed that 52%of patients treatedwithetanercept, 59% treated with adalimumab, 69%Y75%treated with ustekinumab, and 80% treated with infliximabachieved PASI 75 responses with a standard course oftherapy (Reich, Burden, Eaton, & Hawkins, 2012).
TABLE
2.Curren
tTrea
tmen
tsforPsoriasis,Continued
Drug
Brand
Name
ModeofA
ctio
nDosa
ge/A
dministra
tion
Contraindicatio
nsSideEffects
Comments
Secuk
inum
ab
Cose
ntyx
(Nova
rtis)
Humanmonoclona
lantib
odytargetin
gIL-17A
SCinjectio
nof3
00mg
atW
eeks
0,1,
2,3,
and
4,thenonce
eve
ry4weeks
Cautio
nshould
be
used
whe
nco
nsidering
usein
patie
ntswith
chronicinfectio
nora
history
ofrecurrent
infectio
nand
inpatie
ntswith
active
Crohn’sdise
ase
Naso
pha
ryng
itis,
diarrh
ea,a
nd
upperresp
iratory
tractinfectio
n
Inclinicaltria
ls,È80
%ofp
atie
ntsachieve
dPA
SI75
after1
2weeks,a
ndÈ67
%ofp
atie
ntsachieve
dIG
Aofc
learo
ralm
ostclear
Ustekinumab
Stelara
(Janssen)
Humanmonoclona
lantib
odytargetin
gthep40
subunit
ofIL-12
andIL-23
SCinjectio
nsatW
eeks
0and
4,theneve
ry12
weeks
of4
5mgifweighte
220lbs
or9
0mgifweight
922
0lbs
Activ
einfectio
ns,
history
of
recurrent
infectio
ns
Upperresp
iratory
infections,h
eadach
e,fatig
ue,redness
atinjectio
nsite,
backpain
Inclinicaltria
ls,È67
%ofp
atie
ntsachieve
dPA
SI75
after1
2weeks
None
ofthe
agentsa
reapprove
dforu
seinchildrenwith
psoria
sis(C
osentyx
[secuk
inum
ab]injectio
nprescrib
inginform
atio
n,20
15;D
ovo
nex[calcipotriene
]cream
prescrib
inginform
atio
n,20
09;Ladizinskieta
l.,presc
ribinginform
atio
n,20
13;N
PF,p
resc
ribinginform
atio
n,n.d.-a
;Otezla
[apremila
st]tabletspresc
ribinginform
atio
n,2
014;
Tazo
rac[taza
rotene
]cream
presc
ribinginform
atio
n,20
11;V
ectic
al[calcitriol]
ointm
entp
resc
ribinginform
atio
n,2
012;
Zithranol-R
R[a
nthralin]cream
presc
ribinginform
atio
n,2
009).IGA
=inve
stigator’sglobala
ssessment;IL=interle
ukin;IV=intrave
nous;OTC
=ove
r-the-counte
r;PA
SI=Psoria
sisAreaandSe
verityIndex;
PUVA
=pso
ralenplusultravioletlig
ht;RR=rapid
release
;SC
=su
bcuta
neous;TN
F=tumorn
ecrosisfa
cto
r.
VOLUME 8 | NUMBER 1 | JANUARY/FEBRUARY 2016 37
Copyright © 2016 Dermatology Nurses' Association. Unauthorized reproduction of this article is prohibited.
Overall, many experts believe that, over the last 10 years,biologic agents have revolutionized the treatment ofmoderate-to-severe psoriasis because available biologics target cyto-kines that regulate the immune system and control theunderlying pathogenesis of psoriasis (Sivamani et al., 2013).As further improvements have been made in the under-standing of psoriasis, new cytokines have been identifiedas potential targets for drug development (Chiricozzi &Krueger, 2013). Drugs designed to address these and futuretargets may provide new solutions for disease managementand have the potential to positively impact the patientexperience. The next section will review the immunologyof psoriasis, highlighting how existing biologics functionand how new biologics in development target key inflam-matory pathways associated with psoriatic activity.
PSORIASIS IMMUNOLOGY AND THE RATIONALE FORTODAY’S (AND TOMORROW’S) BIOLOGICSImmune responses in the skin provide critical defenseagainst microbial pathogens and chemical and physicalinsults; however, when skin immune responses are excessive,chronic inflammation can result, such as that observed inpsoriasis (Nestle, Di Meglio, Qin, & Nickoloff, 2009).Figure 1 presents a model of psoriasis immunopathogenesisillustrating that, in genetically predisposed individuals,environmental factors andother triggers can initiate psoriasisby instigating the production of multiple cytokines asso-ciated with plaque formation (Lynde, Poulin, Vender,Bourcier, & Khalil, 2014; Nestle et al., 2009). Specifically,stressed keratinocytes trigger production of IL-1", IL-6, andTNF!, and keratinocyte self-DNA forms complexes with
FIGURE 1. Psoriasis immunopathogenesis. Reprinted with permission from Macmillan Publishers Ltd. (Nestle et al., 2009).
38 Journal of the Dermatology Nurses’ Association
Copyright © 2016 Dermatology Nurses' Association. Unauthorized reproduction of this article is prohibited.
antimicrobial peptides to activate plasmacytoid dendriticcells to produce interferon-!. In turn, these cytokines that areproduced in response to stimulus activate dermal dendriticcells (Lynde et al., 2014; Nestle et al., 2009). In addition,other unknown factors may activate dendritic cells, whichmay explain observed psoriatic plaque formation in theabsence of a defined stimulus (Nickoloff & Nestle, 2004).
Activated dendritic cells in the dermis secrete IL-12 andIL-23, which promote differentiation and proliferation ofnaiveTcells into helperT1 (TH1) and TH17 cells, respectively(Lynde et al., 2014; Nestle et al., 2009). When matured,TH17 cells secrete IL-17A, IL-17F, and IL-22, which stimu-late keratinocyte proliferation and release of antimicrobialpeptides, neutrophil-recruiting chemokines, and growthfactors, thus promoting progression of psoriatic plaqueformation and activation of additional dendritic cells andT cells. These events result in a self-reinforcing cascade or‘‘vicious cycle’’ of cytokine production and cell activation.
Cytokines targeted by available biologicsVTNF!, IL-12,IL-23, and IL-17AVare involved in many of the afore-mentioned processes (Lynde et al., 2014; Nestle et al.,2009; Nickoloff & Nestle, 2004). TNF!, as a broadlyacting cytokine mediator of inflammatory and immuneresponses, is secreted by a number of other cell types (e.g.,macrophages, mast cells, natural killer [NK] cells, andgranulocytes) and thus may be associated with the initialresponse to the events precipitating keratinocyte hyperpro-liferation and formation of psoriatic plaque as well as theinflammation associated with both psoriasis and psoriaticarthritis (Croft, Benedict, & Ware, 2013; Ware, 2013).TNF! is involved inmany pathways in the self-reinforcingcascade, and biologics targeting these cytokines are de-signed to disturb these processes and help restore skin toa more normal, nonpsoriatic state (Marble, Gordon, &Nickoloff, 2007; Yost & Gudjonsson, 2009).
IL-12 and IL-23 are also key cytokine mediators ofcellular immunity. Dendritic cells, macrophages, and kera-tinocytes produce IL-12 in response to microbial stimula-tion, which triggers induction of lymphokine-activatedkiller cells, activation of NK cells and T lymphocytes, anddifferentiation of naive T cells to TH1 cells (Benson et al.,2011; Torti & Feldman, 2007). Activated NK cells andTH1 cells then induce T-cell migration to the epidermisand stimulate keratinocyte proliferation (Torti & Feldman,2007). IL-23, together with other cytokines includingIL-1", IL-6, and transforming growth factor-", promotesdifferentiation of naive Tcells to TH17 cells (Benson et al.,2011; Damsker, Hansen, & Caspi, 2010). Continued IL-23signaling is also critical for survival and proliferation ofmature TH17 cells (Damsker et al., 2010). These TH17cells are central drivers of inflammation and immune re-sponses, and the IL-23/TH17 pathway is recognized as amajor immune pathway in the pathogenesis of psoriasis(Chiricozzi & Krueger, 2013; Damsker et al., 2010). Thebiologic agent ustekinumab binds to the common p40subunit of IL-12 and IL23, thereby blocking the down-
stream signaling of both cytokines in the psoriasis cas-cade and providing significant improvements in the clinicalsymptoms of psoriasis (Benson et al., 2011; Leonardi et al.,2008; Papp et al., 2008).
New psoriasis treatment strategies are focused on dis-rupting mechanistic pathways associated with the develop-ment or severity of immunologic responses occurring earlyin the sequence of events leading to plaque formation. Forexample, the recently Food and Drug Administration-approved phosphodiesterase-4 inhibitor (apremilast), onthe basis of its ability to potentially block the productionof proinflammatory cytokines (Schafer, 2012), and kinaseinhibitors (e.g., tofacitinib) are being investigated based onthe rationale that these small molecules will dampen thecellular responses to various cytokines produced in thiscascade (Ortiz-IbaDez et al., 2013). Apremilast acts upstreamin the psoriasis inflammatory cascade to decrease expressionof inducible nitric oxide synthase, TNF!, and IL-23, andit acts to increase expression of IL-10 (Schafer, 2012).Tofacitinib also targets initial immune responses by sup-pressing IL-2, IL-4, IL-7, IL-9, IL-15, and IL-21 andinhibiting the differentiation of TH cells (TH1, TH2, andTH17; Ghoreschi et al., 2011; Ortiz-IbaDez et al., 2013).
Recent studies have highlighted IL-17A as a centraldriver of altered skin function in the pathogenic pathwaysof psoriasis and have made this cytokine an importantdownstream target for agents in development (Chiricozziet al., 2011; Chiricozzi & Krueger, 2013; Gaffen, 2011;Krueger et al., 2012). In addition to being a key productof TH17 cells, IL-17A is produced by neutrophils, mastcells, and cytotoxic T cells (TC17 cells), all of which arefound in excess in psoriatic lesions (Girolomoni et al.,2012; Res et al., 2010). Dermal ,& T cells are also foundin higher levels in psoriatic lesions compared with healthyskin; these proinflammatory cells produce IL-17A in re-sponse to IL-23 and/or IL-1" stimulation (Cai et al., 2011;Cai, Fleming, & Yan, 2013; Laggner et al., 2011).
Numerous roles of IL-17A have been identified in thepathogenesis of psoriasis: recruitment of myeloid dendriticcells and activated TH17 cells to psoriatic lesions, upregu-lation of neutrophil-chemoattracting chemokines on kera-tinocytes, stimulation of antimicrobial peptide expressionon keratinocytes, stimulation of IL-36 expression by kera-tinocytes, disruption of skin barriers, upregulation of IL-6production by fibroblasts and myeloid dendritic cells, up-regulation of IL-1 and IL-23, and chemokine (C-C motif)ligand 20 production by keratinocytes (Girolomoni et al.,2012; Marwaha, Leung, McMurchy, & Levings, 2012).In addition, synergistic action of IL-17A with TNF! hasbeen observed to promote TH17 cell-driven inflammation(Girolomoni et al., 2012; Marwaha et al., 2012).
There are several possible advantages of targeting IL-17Ainstead of more broadly acting upstream cytokines. Forexample, targeting IL-17A has the potential to reducepsoriatic skin inflammation while leaving other immunefunctions undisturbed (Girolomoni et al., 2012; Patel, Lee,
VOLUME 8 | NUMBER 1 | JANUARY/FEBRUARY 2016 39
Copyright © 2016 Dermatology Nurses' Association. Unauthorized reproduction of this article is prohibited.
Kolbinger,&Antoni, 2013). In addition, because it is moreintrinsically involved in formation of the psoriatic plaque,targeting IL-17Amay result in fewer broad immune systemside effects (e.g., serious infection, malignancies) comparedwith blocking TNF! or IL-12 and IL-23 (Girolomoni et al.,2012). Further research will provide the necessary datato help clinicians determine if agents targeting IL-17Ahave a different safety profile from other biologics.
One biologic that targets IL-17 has been approved(secukinumab), and another is currently in clinical devel-opment (ixekizumab). Secukinumab is a human immu-noglobulin (Ig)G10 monoclonal antibody that selectivelybinds and neutralizes IL-17A (Hueber et al., 2010; Langleyet al., 2014). Ixekizumab is a humanized IgG4 monoclonalantibody that binds and neutralizes IL-17A (Krueger et al.,2012; Leonardi et al., 2012). Brodalumab is a fully humanmonoclonal antibody that binds to the receptor subunitIL-17RA, blocking all IL-17 family members that bind tothis receptor, including IL-17A, IL-17C, IL-17F, IL-17A/F,and IL-17E (IL-25). In clinical studies, patients treated withIL-17A inhibitors have experienced rapid and marked im-provements in psoriasis severity (Hueber et al., 2010;Krueger et al., 2012; Langley et al., 2014; Leonardi et al.,2012; Papp et al., 2013); for example, Figure 2 shows onepatient’s clinical response four weeks after receiving asingle infusion of secukinumab in a proof-of-concept study(Hueber et al., 2010). In a Phase 3 study of secukinumabin patients with moderate-to-severe psoriasis, significantimprovements in PASI scores were observed at Week 12compared with placebo and etanercept, and these im-
provements were maintained to 52 weeks (Langley et al.,2014). Interestingly, the clinical improvements observedin patients treated with IL-17A inhibitors correlate withhistological improvements and reduced gene expression(Chiricozzi & Krueger, 2013). In a Phase 2a study inpatients with moderate-to-severe plaque psoriasis, signif-icant PASI improvements observed four weeks after treat-ment with secukinumab were associated with reducedT-cell infiltration in skin lesions and reduced productionof inflammatory cytokines (Hueber et al., 2010). A Phase1 study of ixekizumab in patients withmoderate-to-severeplaque psoriasis also showed that keratinocyte prolifera-tion, hyperplasia, epidermal thickness, and keratinocyteexpression of innate defense peptides were reduced twoweeks after dosing, and normal histological skin appear-ance was achieved by Week 6 (Krueger et al., 2012).Overall, the investigational agents targeting IL-17A havebeen generally well tolerated in early-stage clinical studieswithout unexpected safety signals (Leonardi et al., 2012;Papp et al., 2013; Rich et al., 2013). However, larger-scale studies are underway to better establish the long-term safety profiles of these agents.
DISCUSSIONBiologics are effective, well-tolerated treatment options forchronic plaque psoriasis that can produce dramatic clinicalimprovements in a relatively short period (Sivamani et al.,2013; Wheeler, 2010). Unlike topical and conventionalsystemic therapies that were discovered serendipitously anddo not specifically address the underlying pathogenesis ofpsoriasis, biologics have been, and continue to be, developedbased on scientific evidence identifying therapeutic targetswithin the critical immune and inflammatory pathwaysassociatedwith the development and progression of disease(Nickoloff & Nestle, 2004). Furthermore, because biologicstarget underlying inflammation, earlier use of biologics mayslow disease progression and prevent inflammatory comor-bidities, such as atherosclerosis and metabolic syndrome(Golden, McCormick, & Ward, 2013).
When selecting appropriate psoriasis therapies, it is im-portant for practitioners to consider a variety of factorssuch as efficacy, onset of action, sustainability of efficacy,route of administration, convenience, safety, and tolera-bility. From a patient perspective, many have referred tobiologics as ‘‘wonder drugs’’ based on the high degree ofskin clearance, relatively few side effects, and convenientadministration (Wheeler, 2010). In addition, results of re-cent surveys evaluating patient experiences with psoriasistreatments have shown that satisfaction with biologics isnotably higher than with topicals or conventional systemictherapies (Callis Duffin et al., 2014; Poulin et al., 2012).Meta-analyses of data from randomized controlled trialsof available biologics have found that infliximab is themost effective TNF! inhibitor (in terms of mean PASI im-provement), and etanercept is the least effective, althoughthe clinical implications of these differences are unclear
FIGURE 2. Clinical response in a patient with chronic plaquepsoriasis after a single intravenous infusion of secukinumab3 mg/kg (Hueber et al., 2010). Reprinted with permission.
40 Journal of the Dermatology Nurses’ Association
Copyright © 2016 Dermatology Nurses' Association. Unauthorized reproduction of this article is prohibited.
(Reich et al., 2012; Schmitt, Zhang, Wozel, Meurer, &Kirch, 2008). Comparative trials may also prove helpfulin choosing among the biologics; however, such studiesare limited to date. Of the few head-to-head trials,secukinumab and ustekinumab were found to be signifi-cantly more effective than etanercept over 12weeks of treat-ment (Griffiths et al., 2010; Langley et al., 2014). Theseefficacy differences may be explained, in part, by differ-ences in pharmacokinetic properties. Etanercept is clearedfrom serum roughly six times faster than adalimumab orinfliximab and has a shorter half-life (4 days for etanerceptcompared with 8Y10 days for infliximab, 10Y20 days foradalimumab, È21 days for ustekinumab, and È28 daysfor secukinumab; Baeten et al., 2010; Benson et al., 2011;Ware, 2013). Additionally, secukinumab was found to besignificantlymore effective than ustekinumab after 16weeksof treatment (Thaci et al., 2015).
In terms of safety, all available biologics are generallywell tolerated, and although biologics may increase pa-tients’ risk of serious infection andmalignancy, these eventsare rare (Dommasch et al., 2011). Infliximab is associatedwith the highest risk of neutralizing antibodies because itis a human-murine chimeric monoclonal anti-TNF anti-body, producing the risk for an infusion reaction or loss ofbenefit requiring a dose adjustment or other change. Incontrast, etanercept is a chimeric fusion of the human TNFreceptor with an antibody Fc fragment, and adalimumab,secukinumab, and ustekinumab are human IgG1 antibodies(Benson et al., 2011; Langley et al., 2014; Ware, 2013; Yost& Gudjonsson, 2009).
All available biologics, with the exception of infliximab,are administered subcutaneously, with initial dosing sched-ules ranging from twice weekly (etanercept) to once everyfour weeks (secukinumab and ustekinumab) with less fre-quent dosing over time for most agents (Langley et al.,2014; Sivamani et al., 2013). Infliximab is administeredby intravenous injection, as two initial injections twoweeksapart followed by dosing every 12 weeks (Sivamani et al.,2013). Survey results indicate that patients rate the con-venience of self-administered subcutaneous biologics higherthan intravenous infliximab (Callis Duffin et al., 2014).
Overall, it is important to have multiple treatment op-tionswith different mechanisms of action, as not all agentswork for all patients, and switching from one biologic toanother is a valid strategy when patients fail to respond orlose the response to any given agent (Gottlieb et al., 2012;Strober et al., 2011). Furthermore, psoriasis is a lifelong,chronic disease, and over time,many patientswill likely needto access numerous therapies for a host of reasons, such asloss of efficacy, comorbidities, life changes, development ofside effects, cost/insurance issues, and convenience. Devel-opment of drugs that target new pathways in psoriasis willincrease the number of options practitioners have to moreeffectively treat this complex disease in more patients.
Improved understanding of psoriasis as a chronic sys-temic disease and of the pathways responsible for the
manifestation of psoriatic plaques and inflammation hasprovided scientists with the opportunity to develop agentswith more specific targets. Clinicians, patients, and in-vestigators are hopeful that the results from early-stageclinical trials of newer agents will be confirmed in late-stage development. If this is the case, new treatments willjoin the most recently approved biologic, secukinumab, asadditions to an ever-expanding psoriasis armamentariumVprogress that should continue toopennew, life-changingdoorsfor patients with all types and degrees of psoriatic disease.h
REFERENCES
Aaronson, D. S., & Lebwohl, M. (2004). Review of therapy of psoriasis: Theprebiologic armamentarium. Dermatologic Clinics, 22(4), 379Y388, vii.
American Academy of Dermatology and AAD Association. (2013).Position statement on treatment of psoriatic patients. Retrieved fromhttp:/ /www.aad.org/Forms/Policies/Uploads/PS/PS%20on%20Treatment%20of%20Psoriatic%20Patients.pdf
Armstrong, A.W., Robertson, A. D., Wu, J., Schupp, C., & Lebwohl, M. G.(2013). Undertreatment, treatment trends, and treatment dissatisfactionamong patients with psoriasis and psoriatic arthritis in the United States:Findings from the National Psoriasis Foundation surveys, 2003Y2011.JAMA Dermatology, 149(10), 1180Y1185.
Baeten, D., Sieper, J., Emery, P., Braun, J., Van der Heijde, D., McInnes, I.,I Hueber, W. (2010). The anti-IL17A monoclonal antibodysecukinumab (AIN457) showed good safety and efficacy in the treatmentof active ankylosing spondylitis [abstract L7]. Arthritis and Rheumatol-ogy, 62(12), 3840.
Baker, C., Mack, A., Cooper, A., Fischer, G., Shumack, S., Sidhu, S., IFoley, P. (2013). Treatment goals for moderate to severe psoriasis: AnAustralian consensus. The Australasian Journal of Dermatology, 54(2),148Y154.
Barker, J., Hoffmann, M., Wozel, G., Ortonne, J. P., Zheng, H.,vanHoogstraten, H., & Reich, K. (2011). Efficacy and safety of infliximabvs. methotrexate in patients with moderate-to-severe plaque psoriasis: Re-sults of an open-label, active-controlled, randomized trial (RESTORE1).The British Journal of Dermatology, 165(5), 1109Y1117.
Benson, J. M., Peritt, D., Scallon, B. J., Heavner, G. A., Shealy, D. J.,Giles-Komar, J.M., &Mascelli, M. A. (2011). Discovery and mechanismof ustekinumab: A human monoclonal antibody targeting interleukin- 12and interleukin-23 for treatment of immune-mediated disorders. mAbs,3(6), 535Y545.
Bilac, C., Ermertcan, A. T., Bilac, D. B., Deveci, A., & Horasan, G. D.(2009). The relationship between symptoms and patient characteristicsamong psoriasis patients. Indian Journal of Dermatology, Venereologyand Leprology, 75(5), 551.
Cai, Y., Fleming, C., & Yan, J. (2013). Dermal +% T cellsVA new player inthe pathogenesis of psoriasis. International Immunopharmacology,16(3), 388Y391.
Cai, Y., Shen, X., Ding, C., Qi, C., Li, K., Li, X., I Yan, J. (2011). Pivotalrole of dermal IL-17-producing +% T cells in skin inflammation.Immunity, 35(4), 596Y610.
Callis Duffin, K., Yeung, H., Takeshita, J., Krueger, G. G., Robertson, A. D.,Troxel, A. B., I Gelfand, J. M. (2014). Patient satisfaction with treat-ments for moderate-to-severe plaque psoriasis in clinical practice. TheBritish Journal of Dermatology, 170(3), 672Y680.
Chiricozzi, A., Guttman-Yassky, E., Suarez-FariDas, M., Nograles, K. E.,Tian, S., Cardinale, I., I Krueger, J. G. (2011). Integrative responsesto IL-17 and TNF-! in human keratinocytes account for key inflamma-tory pathogenic circuits in psoriasis. The Journal of Investigative Derma-tology, 131(3), 677Y687.
Chiricozzi, A., & Krueger, J. G. (2013). IL-17 targeted therapies forpsoriasis. Expert Opinion on Investigational Drugs, 22(8), 993Y1005.
Christophers, E., Griffiths, C. E., Gaitanis, G., & van de Kerkhof, P.(2006). The unmet treatment need for moderate to severe psoriasis:Results of a survey and chart review. Journal of the European Academyof Dermatology and Venereology, 20(8), 921Y925.
Cosentyx (secukinumab) injection [prescribing information]. (2015). EastHanover, NJ: Novartis Pharmaceuticals Corporation.
Croft,M., Benedict, C. A., &Ware, C. F. (2013). Clinical targeting of the TNFand TNFR superfamilies.Nature Reviews, Drug Discovery, 12(2), 147Y168.
VOLUME 8 | NUMBER 1 | JANUARY/FEBRUARY 2016 41
Copyright © 2016 Dermatology Nurses' Association. Unauthorized reproduction of this article is prohibited.
Damsker, J. M., Hansen, A. M., & Caspi, R. R. (2010). Th1 and Th17cells: Adversaries and collaborators. Annals of the New York Academyof Sciences, 1183, 211Y221.
Dommasch, E. D., Abuabara, K., Shin, D. B., Nguyen, J., Troxel, A. B., &Gelfand, J. M. (2011). The risk of infection and malignancy with tumornecrosis factor antagonists in adults with psoriatic disease: A systematicreview and meta-analysis of randomized controlled trials. Journal of theAmerican Academy of Dermatology, 64(6), 1035Y1050.
Dovonex (calcipotriene) cream [prescribing information]. (2009). Parsippany,NJ: Leo Pharma, Inc.
Enbrel (etanercept) solution [prescribing information]. (2015). ThousandOaks, CA: Immunex Corporation.
Gaffen, S. L. (2011). Recent advances in the IL-17 cytokine family. CurrentOpinion in Immunology, 23(5), 613Y619.
Gelfand, J. M., & Yeung, H. (2012). Metabolic syndrome in patients withpsoriatic disease. The Journal of Rheumatology, 89, 24Y28.
Ghoreschi, K., Jesson, M. I., Li, X., Lee, J. L., Ghosh, S., Alsup, J. W., IO’Shea, J. J. (2011). Modulation of innate and adaptive immune re-sponses by tofacitinib (CP-690,550). Journal of Immunology, 186(7),4234Y4243.
Girolomoni, G., Mrowietz, U., & Paul, C. (2012). Psoriasis: Rationale fortargeting interleukin-17. The British Journal of Dermatology, 167(4),717Y724.
Golden, J. B., McCormick, T. S., & Ward, N. L. (2013). IL-17 in psoriasis:Implications for therapy and cardiovascular co-morbidities. Cytokine,62(2), 195Y201.
Gottlieb, A., Korman, N. J., Gordon, K. B., Feldman, S. R., Lebwohl, M.,Koo, J. Y., I Menter, A. (2008). Guidelines of care for the managementof psoriasis and psoriatic arthritis: Section 2. Psoriatic arthritis: Overviewand guidelines of care for treatment with an emphasis on the biologics.Journal of the American Academy of Dermatology, 58(5), 851Y864.
Gottlieb, A. B., Kalb, R. E., Blauvelt, A., Heffernan, M. P., Sofen, H. L.,Ferris, L. K.,I Chevrier, M. (2012). The efficacy and safety of infliximabin patients with plaque psoriasis who had an inadequate response toetanercept: Results of a prospective, multicenter, open-label study. Journalof the American Academy of Dermatology, 67(4), 642Y650.
Griffiths, C. E., Strober, B. E., van de Kerkhof, P., Ho, V., Fidelus-Gort, R.,Yeilding, N., ... ACCEPT Study Group. (2010). Comparison ofustekinumab and etanercept for moderate-to-severe psoriasis. The NewEngland Journal of Medicine, 362(2), 118Y128.
Horn, E. J., Fox, K. M., Patel, V., Chiou, C. F., Dann, F., & Lebwohl, M.(2007). Are patients with psoriasis undertreated? Results of NationalPsoriasis Foundation survey. Journal of the American Academy ofDermatology, 57(6), 957Y962.
Hueber, W., Patel, D. D., Dryja, T., Wright, A. M., Koroleva, I., Bruin, G.,I Di Padova, F. (2010). Effects of AIN457, a fully human antibody tointerleukin-17A, on psoriasis, rheumatoid arthritis, and uveitis. ScienceTranslational Medicine, 2(52), 52ra72.
Humira (adalimumab) injection [prescribing information]. (2014). NorthChicago, IL: AbbVie, Inc.
Kimball, A. B., Gladman, D., Gelfand, J. M., Gordon, K., Horn, E. J.,Korman, N. J., I National Psoriasis Foundation. (2008). NationalPsoriasis Foundation clinical consensus on psoriasis comorbidities andrecommendations for screening. Journal of the American Academy ofDermatology, 58(6), 1031Y1042.
Kimball, A. B., Jacobson, C., Weiss, S., Vreeland, M. G., & Wu, Y. (2005).The psychosocial burden of psoriasis. American Journal of ClinicalDermatology, 6(6), 383Y392.
Krueger, J. G., Fretzin, S., Suarez-FariDas, M., Haslett, P. A., Phipps, K. M.,Cameron, G. S., I Hoffman, R. W. (2012). IL-17A is essential for cellactivation and inflammatory gene circuits in subjects with psoriasis. TheJournal of Allergy and Clinical Immunology, 130(1), 145.e9Y154.e9.
Ladizinski, B., Lee, K. C., Wilmer, E., Alavi, A., Mistry, N., & Sibbald, R. G.(2013). A review of the clinical variants and the management of psoriasis.Advances in Skin & Wound Care, 26(6), 271Y284.
Laggner, U., Di Meglio, P., Perera, G. K., Hundhausen, C., Lacy, K. E., Ali, N.,I Nestle, F. O. (2011). Identification of a novel proinflammatory humanskin-homing V+9V%2 T cell subset with a potential role in psoriasis.Journal of Immunology, 187(5), 2783Y2793.
Langley, R. G., Elewski, B. E., Lebwohl, M., Reich, K., Griffiths, C. E.,Papp, K., I FIXTURE Study Group. (2014). Secukinumab in plaquepsoriasisVResults of two phase 3 trials. The New England Journal ofMedicine, 371(4), 326Y338.
Lee, S., Coleman, C. I., Limone, B., Kaur, R., White, C. M., Kluger, J., &Sobieraj, D. M. (2012). Biologic and nonbiologic systemic agents andphototherapy for treatment of chronic plaque psoriasis. Comparativeeffectiveness review no. 85 (prepared by the University of Connecticut/
Hartford Hospital Evidence-based Practice Center under contract no.290-2007-10067-I) (No. AHRQ Publication No.12(13)-EHC144-EF).Rockville, MD. Retrieved from http://effectivehealthcare.ahrq.gov/ehc/products/312/1325/CER85_ChronicPlaquePsoriasis_FinalReport_20121119.pdf
Leonardi, C., Matheson, R., Zachariae, C., Cameron, G., Li, L.,Edson-Heredia, E., I Banerjee, S. (2012). Anti-interleukin-17 monoclo-nal antibody ixekizumab in chronic plaque psoriasis. The New EnglandJournal of Medicine, 366(13), 1190Y1199.
Leonardi, C. L., Kimball, A. B., Papp, K. A., Yeilding, N., Guzzo, C.,Wang, Y., I PHOENIX 1 Study Investigators. (2008). Efficacy andsafety of ustekinumab, a human interleukin-12/23 monoclonal anti-body, in patients with psoriasis: 76-week results from a randomised,double-blind, placebo-controlled trial (PHOENIX 1). Lancet, 371(9625),1665Y1674.
Ljosaa, T.M., Rustoen, T., MPrk, C., Stubhaug, A., Miaskowski, C., Paul, S. M.,& Wahl, A. K. (2010). Skin pain and discomfort in psoriasis: An explor-atory study of symptom prevalence and characteristics. Acta Dermato-Venereologica, 90(1), 39Y45.
Lynde, C. W., Poulin, Y., Vender, R., Bourcier, M., & Khalil, S. (2014).Interleukin 17A: Toward a new understanding of psoriasis pathogenesis.Journal of the American Academy of Dermatology, 71(1), 141Y150.
Mallbris, L., Larsson, P., Bergqvist, S., Ving*rd, E., Granath, F., & St*hle, M.(2005). Psoriasis phenotype at disease onset: Clinical characterizationof 400 adult cases. The Journal of Investigative Dermatology, 124(3),499Y504.
Marble, D. J., Gordon, K. B., & Nickoloff, B. J. (2007). TargetingTNFalpha rapidly reduces density of dendritic cells and macrophagesin psoriatic plaques with restoration of epidermal keratinocytedifferentiation. Journal of Dermatological Science, 48(2), 87Y101.
Marwaha, A. K., Leung, N. J., McMurchy, A. N., & Levings, M. K.(2012). TH17 cells in autoimmunity and immunodeficiency: Protectiveor pathogenic? Frontiers in Immunology, 3, 129.
Menter, A., Gottlieb, A., Feldman, S. R., Van Voorhees, A. S., Leonardi, C. L.,Gordon, K. B., I Bhushan, R. (2008). Guidelines of care for the man-agement of psoriasis and psoriatic arthritis: Section 1. Overview of pso-riasis and guidelines of care for the treatment of psoriasis with biologics.Journal of the American Academy of Dermatology, 58(5), 826Y850.
Mrowietz, U., Kragballe, K., Reich, K., Spuls, P., Griffiths, C. E., Nast, A.,I Yawalkar, N. (2011). Definition of treatment goals for moderate tosevere psoriasis: A European consensus. Archives of DermatologicalResearch, 303(1), 1Y10.
National Psoriasis Foundation. (2008). Psoriasis on specific skin sites.Retrieved from http://www.psoriasis.org/document.doc?id=157
National Psoriasis Foundation. (2013). Fact sheet. Retrieved from http://www.psoriasis.org/document.doc?id=883
National Psoriasis Foundation. (n.d.-a). Psoriasis treatments. Retrievedfrom http://www.psoriasis.org/about-psoriasis/treatments
National Psoriasis Foundation. (n.d.-b). Statistics. Retrieved from http://www.psoriasis.org/research/science-of-psoriasis/statistics
Nestle, F. O., Di Meglio, P., Qin, J. Z., & Nickoloff, B. J. (2009). Skin immunesentinels in health and disease. Nature Reviews Immunology, 9(10),679Y691.
Nickoloff, B. J., & Nestle, F. O. (2004). Recent insights into theimmunopathogenesis of psoriasis provide new therapeutic opportuni-ties. The Journal of Clinical Investigation, 113(12), 1664Y1675.
Ortiz-IbaDez, K., Alsina, M. M., & MuDoz-Santos, C. (2013). Tofacitiniband other kinase inhibitors in the treatment of psoriasis. Actas Dermo-Sifiliograficas, 104(4), 304Y310.
Ortleb, M., & Levitt, J. O. (2012). Practical use of biologic therapy indermatology: Some considerations and checklists. Dermatology OnlineJournal, 18(2), 2.
Otezla (apremilast) tablets [prescribing information]. (2014). Summit, NJ:Celgene Corporation.
Papp, K. A., Langley, R. G., Lebwohl, M., Krueger, G. G., Szapary, P.,Yeilding, N., ... PHOENIX 2 Study Investigators. (2008). Efficacy andsafety of ustekinumab, a human interleukin-12/23 monoclonal antibody,in patients with psoriasis: 52-week results from a randomised, double-blind,placebo-controlled trial (PHOENIX 2). Lancet, 371(9625), 1675Y1684.
Papp, K. A., Langley, R. G., Sigurgeirsson, B., Abe, M., Baker, D. R.,Konno, P., I Richards, H. B. (2013). Efficacy and safety ofsecukinumab in the treatment of moderate-to-severe plaque psoriasis: Arandomized, double-blind, placebo-controlled phase II dose-rangingstudy. The British Journal of Dermatology, 168(2), 412Y421.
Pariser, D. M., Bagel, J., Gelfand, J. M., Korman, N. J., Ritchlin, C. T.,Strober, B. E., I National Psoriasis Foundation. (2007). National
42 Journal of the Dermatology Nurses’ Association
Copyright © 2016 Dermatology Nurses' Association. Unauthorized reproduction of this article is prohibited.
Psoriasis Foundation clinical consensus on disease severity. Archives ofDermatology, 143(2), 239Y242.
Patel, D. D., Lee, D. M., Kolbinger, F., & Antoni, C. (2013). Effect of IL-17Ablockade with secukinumab in autoimmune diseases. Annals of theRheumatic Diseases, 72(Suppl. 2), ii116Yii123.
Poulin, Y., Wasel, N., Chan, D., Bernstein, G., Andrew, R., Fraquelli, E., &Papp, K. (2012). Evaluating practice patterns for managing moderateto severe plaque psoriasis: Role of the family physician. CanadianFamily Physician, 58(7), e390Ye400.
Reich, K., Burden, A. D., Eaton, J. N., & Hawkins, N. S. (2012). Efficacyof biologics in the treatment of moderate to severe psoriasis: A networkmeta-analysis of randomized controlled trials. The British Journal ofDermatology, 166(1), 179Y188.
Remicade (infliximab) lyophilized concentrate for injection [prescribinginformation]. (2015). Horsham, PA: Janssen Biotech, Inc.
Res, P. C., Piskin, G., de Boer, O. J., van der Loos, C. M., Teeling, P., Bos, J. D.,& Teunissen, M. B. (2010). Overrepresentation of IL-17A and IL-22producing CD8 T cells in lesional skin suggests their involvement in thepathogenesis of psoriasis. PloS One, 5(11), e14108.
Rich, P., Sigurgeirsson, B., Thaci, D., Ortonne, J. P., Paul, C., Schopf, R. E.,I Papavassilis, C. (2013). Secukinumab induction and maintenancetherapy in moderate-to-severe plaque psoriasis: A randomized, double-blind, placebo-controlled, phase II regimen-finding study. The BritishJournal of Dermatology, 168(2), 402Y411.
Saurat, J. H., Stingl, G., Dubertret, L., Papp, K., Langley, R. G., Ortonne, J. P.,I CHAMPION Study Investigators. (2008). Efficacy and safety resultsfrom the randomized controlled comparative study of adalimumab vs.methotrexate vs. placebo in patients with psoriasis (CHAMPION). TheBritish Journal of Dermatology, 158(3), 558Y566.
Schafer, P. (2012). Apremilast mechanism of action and application topsoriasis and psoriatic arthritis. Biochemical Pharmacology, 83(12),1583Y1590.
Schmitt, J., Zhang, Z., Wozel, G., Meurer, M., & Kirch, W. (2008).Efficacy and tolerability of biologic and nonbiologic systemic treatmentsfor moderate-to-severe psoriasis: Meta-analysis of randomized controlledtrials. The British Journal of Dermatology, 159(3), 513Y526.
Schmitt, J.M., & Ford, D. E. (2006). Work limitations and productivity lossare associated with health-related quality of life but not with clinicalseverity in patients with psoriasis. Dermatology, 213(2), 102Y110.
Sivamani, R. K., Goodarzi, H., Garcia, M. S., Raychaudhuri, S. P., Wehrli, L. N.,Ono, Y., & Maverakis, E. (2013). Biologic therapies in the treatment of
psoriasis: A comprehensive evidence-based basic science and clinicalreview and a practical guide to tuberculosis monitoring. Clinical Reviewsin Allergy & Immunology, 44(2), 121Y140.
Stelara (ustekinumab) injection [prescribing information]. (2014). Horsham,PA: Janssen Biotech, Inc.
Stern, R. S., Nijsten, T., Feldman, S. R., Margolis, D. J., & Rolstad, T.(2004). Psoriasis is common, carries a substantial burden even when notextensive, and is associated with widespread treatment dissatisfaction.The Journal of Investigative Dermatology, 9(2), 136Y139.
Strober, B. E., Poulin, Y., Kerdel, F. A., Langley, R. G., Gu, Y., Gupta, S. R.,I Papp, K. A. (2011). Switching to adalimumab for psoriasis patientswith a suboptimal response to etanercept, methotrexate, or phototherapy:Efficacy and safety results from an open-label study. Journal of theAmerican Academy of Dermatology, 64(4), 671Y681.
Tazorac (tazarotene) cream [prescribing information]. (2011). Irvine, CA:Allergan, Inc.
Thaci, D., Blauvelt, A., Reich, K., Tsai, T. F., Vanaclocha, F., Kingo, K., IMilutinovic, M. (2015). Secukinumab is superior to ustekinumab inclearing skin of subjects with moderate to severe plaque psoriasis: CLEAR,a randomized controlled trial. Journal of the American Academy ofDermatology, 73(3), 400Y409.
Torti, D. C., & Feldman, S. R. (2007). Interleukin-12, interleukin-23, andpsoriasis: Current prospects. Journal of the American Academy ofDermatology, 57(6), 1059Y1068.
Vectical (calcitriol) ointment [prescribing information]. (2012). Fort Worth,TX: Galderma Laboratories, L.P.
VillaseDor-Park, J., Wheeler, D., & Grandinetti, L. (2012). Psoriasis: Evolvingtreatment for a complex disease. Cleveland Clinic Journal of Medicine,79(6), 413Y423.
Ware, C. F. (2013). Protein therapeutics targeted at the TNF superfamily.Advances in Pharmacology, 66, 51Y80.
Wheeler, T. (2010). Psoriasis: Impact and management of moderate to severedisease. British Journal of Nursing, 19(1), 10Y17.
Yost, J., & Gudjonsson, J. E. (2009). The role of TNF inhibitors in psoriasistherapy: New implications for associated comorbidities. F1000 MedicineReports, 1, pii: 30. doi:10.3410/M3411-3430
Young, M. (2005). The psychological and social burdens of psoriasis. Der-matology Nursing, 17(1), 15Y19.
Zithranol-RR (anthralin) cream [prescribing information]. (2009). VernonHills, IL: Elorac, Inc.
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