hcv protease inhibitors in the treatment of naive and … · svr, considered virologic cure, was...
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HCV protease inhibitors in the treatmentof naive and experienced patients
Pr Dominique SalmonCochin Hospital, Paris Descartes University, Paris, France
2nd Congress of Federation of Arab Societies of ClinicalMicrobiology and Infectious Diseases
22nd Tunisian Congress of Infectious Diseases
http://www.infectiologie.org.tn
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World prevalence of HCV
< 1%1 - 2,4%2,5 - 4,9%5 - 10%> 10%Data non available
WHO (97)http://www.infectiologie.org.tn
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Distribution of HCV genotypes
North America
South America
South Africa
Central Africa
North EuropeRussia
ChinaJapan
AustraliaNew Zeland
Sout East Asia
1a 51b 2 3 4 6
Genotypes/sub-types
South Europa
Forns et Bukh (98)http://www.infectiologie.org.tn
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Chronic hepatitis C progression
HCC3%/yr Decompensation
5%- 10%/anLiver mortality
2%- 5%/yr
5- 10 years 15- 30 years >30 years
Rapid Intermediate Slow
Progression speed
Cirrhosis
Fibrosis stage 0
1
2
3
4
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Therapeutic objectives for HIV, HBV and HCV
H
HBV
Host cell
cccDNAHost DNA
Integrated DNA
Nucleus
H
HIVHost cell
Host DNA
Proviral DNA
Nucleus
H
HCVHost cell
Host DNA
Nucleus
HCV RNA
Life long suppression of viral replication
Definitive viral clearanceand SVR
Long term suppression of viral replication
Kieffer et al. J Antimicrob Chemother 2010; Sorriano et al. J Antimicrob Chemother 2009; Clavel et al. New Engl J Med 2004; Zoulim &Locarnini Gastroenterology 2009; Sarrazin & Zeuzem Gastroenterology 2010
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Combinaison of peg interferon and ribavirin: first step towards cure …
PatientsachievingSVR (%)
100
80
60
40
20
024 48 78 Peg-IFN IFN +
ribavirinPeg-IFN +ribavirinWeeks
IFN monotherapy
All genotypesGenotype 1Genotypes 2 or 3
6-19 11-19 10-22
18-3935-43
61-79
33-36
76-82
42-46
*Range of values reported; lower bar represents lower value;
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0%
20%
40%
60%
80%
100%
IFN 24 wk IFN 48 wk
IFN 48 wk& Ribavirin
PEG-IFN 48 wk& Ribavirin
1990 1998 2000 2002 2012- 2015
Sustained VirologicalResponses Rates
Direct antivirals
2007
Future of anti HCV therapy
Optimization and individualization
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Better knowledge of HCV enzymes targeted by specific inhibitors
Di Bisceglie et al., Hepatology 2002http://www.infectiologie.org.tn
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Efficacy of with HCV protease inhibitors with peg interferon and ribavirin in NAIVE
patients infected with genotype 1
http://www.infectiologie.org.tn
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Peg-IFNα-2a + RBV
Peg-IFNα-2a + RBV
eRVR*
YES
NO
Telaprevir1,2
Short duration (24W): 59–65%SVR: 89–92%
SVR: 54–64%
* HCV RNA <25 IU/mL at wks 4 and 12
1. Jacobson IM, et al. Hepatology 2010; 52 (S1) [abstract 211]2. Sherman KE, et al. Hepatology 2010; 52 (S1) [abstract LB-2]
Telaprevir in GT1 treatment-naive patients
0 Weeks 484 8 12 24 28
TPV + Peg-IFNα-2a + RBV
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SVR rate with telaprevir and peginterferon/RBV versus PR
ADVANCE and ILLUMINATE trials
46
0
20
40
60
80
100
SVR
(%)
T12/PR
683/903
PR48
166/361n/N =
74–79*
INCIVO (telaprevir) EU SmPC
*p<0.0001 T12/PR vs PR48 (79% versus 46%) in ADVANCESVR, considered virologic cure, was defined as HCV RNA <25 IU/mL at last observation within the Week 72 visit window. In case of missing data, the last HCV RNA data point from Week 12 of follow-up onwards was usedhttp://www.infectiologie.org.tn
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1. Jacobson IM, et al. Hepatology 2010; 52 (S1) [abstract 211]; 2. Sherman KE, et al. Hepatology 2010; 52 (S1) [abstract LB-2];
3. Poordad F, et al. Hepatology 2010; 52 (S1) [abstract LB-4]
TPV and BOC in GT1 treatment-naive patients
Peg-IFNα-2a + RBV
Peg-IFNα-2a + RBV
eRVR*
YES
NO
Telaprevir1,2
SVR: 54–64%
* HCV RNA <25 IU/mL at wks 4 and 12
0 Weeks 484 8 12 24 28
BOC + Peg-IFNα-2b + RBV
W8–W24 RVR **
BOC + Peg-IFNα-2b + RBV
** HCV RNA <9.3 IU/mL
0 Weeks 484 8 12 24 28
YES
NO
TPV + Peg-IFNα-2a + RBV
P/Rlead-in
BOC +P/R
Boceprevir3
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38
63 66
0
20
40
60
80
100
SVR
(%)
BOC RGT
233/368
BOC44/PR48
242/366
PR48
137/363n/N =
VICTRELIS (boceprevir) EU SmPC
* *
*p<0.001 for both boceprevir arms versus PR48SVR was defined as undetectable HCV RNA at the last available value in the period at or after follow-up Week 24. If there was no such value, the follow-up Week value was carried forward
SVR rate with boceprevir and peginterferon/RBV versus PR
SPRINT 1 and SPRINT 2 trials
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Impact of rapid virologic response on SVR : leading to different durations of treatment
Exemple of telaprevir
Sherman KE, et al. N Engl J Med 2011;365:1014–24
*Patients who achieved eRVR (undetectable HCV RNA at Weeks 4 and 12) and completed the Week 20 visit were randomized to receive an additional 4 or 28 weeks of PR alone65% of patients achieved an eRVR (352/540); 322/352 were randomized and 30/352 patients discontinued before randomization at Week 20
Treatment duration according to eRVR status
60%*n=32222%
n=118
92 88
64
23
0
20
40
60
80
100
SVR
(%)
<20 weeks
23/100
SVR rate
18%n=100
Eligible for 24 weeks and randomized to 24 or 48 weeks*
48 weeks
<20 weeks (due to premature treatment discontinuation)
eRVR+*
eRVR–
<20 weeks
eRVR–T12PR48
76/118
eRVR+ T12PR48140/160
eRVR+ T12PR24149/162
∆ 4% (2-sided 95% CI = –2% to +11%)
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Efficacy of with HCV protease inhibitors with peg interferon and ribavirin in
patients infected with genotype 1, non responders to peg IFN/RBV
http://www.infectiologie.org.tn
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Definitions of non responses to Peg-IFN/RBV
Detection limit
Relapse
Null response
BreakthroughPartial response
Treatment
0 4 8 12 16 20 24 28 32 36 40 44 48 52 56 60 64 68 72
HC
V R
NA
leve
l
Weeks
2 log10 drop
Non-response
Adapted from Shiffman M. Curr Gastroenterol Rep 2006;8:46–52Neumann A, et al. Science 1998;282:103–7; De Bruijne J, et al. Neth J Med 2008;66:311–22http://www.infectiologie.org.tn
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SVR to telaprevir with PR in relapsers, partial responders and null responders to PR
22
88 84
15
5661
5
33 31
0
20
40
60
80
100
PR48
4/27
T12/PR48
30/49
SVR
(%)
Prior relapsers Prior partialresponders
LI T12/PR48
27/48n/N=
PR48
2/37
T12/PR48
22/72
LI T12/PR48
25/75
PR48
15/68
T12/PR48
122/145
LI T12/PR48
124/141
Prior null responders
**
**
* *
INCIVO (telaprevir) EU SmPC
*p<0.001 vs PR48SVR, considered virologic cure, was defined as HCV RNA <25 IU/mL at last observation within the Week 72 visit window. In case of missing data, the last HCV RNA data point from Week 12 of follow-up onwards was usedhttp://www.infectiologie.org.tn
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29
6975
7
40
52
0
20
40
60
80
100
PR48
2/29
BOC44/PR48
30/58
SVR
(%)
Prior relapsers Prior partialresponders
BOCRGT
23/57n/N=
PR48
15/51
BOC44/PR48
77/103
BOC RGT
72/105
Prior null responders were excluded from RESPOND-2
SVR was defined as undetectable HCV RNA at the last available value in the period at or after follow-up Week 24. If there was no such value, the follow-up Week 12 value was carried forward VICTRELIS (boceprevir) EU SmPC
SVR to boceprevir with PR in relapsers and partial responders to PR
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Three main baseline predictors of SVR under tritherapy with PI
HCV viral load
HCV G1 subtype: 1b > 1a
Fibrosis stage
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HCV G1 subtype as a Predictor of SVR (BOC Arms Combined)
20
54
27
43
25
47
0
20
40
60
80
100
% S
VR
1154
1935
33124
44178
2661
4596
1a 1b 1a 1b 1a 1b
RESPOND-2 SPRINT-2 CombinedStudies
p = 0.001 p = 0.028 p < 0.001
Bacon, AASLD, 2011http://www.infectiologie.org.tn
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Fibrosis Score as a Predictor of SVR (BOC Arms Combined)
41
21
37
15
38
17
0
20
40
60
80
100
% S
VR
2663
419
58157
842204
278
46
F0/1/2 F3/4RESPOND-2 SPRINT-2 Combined
Studies
p = 0.11 p = 0.025 p = 0.007
F0/1/2 F3/4 F0/1/2 F3/4
Bacon, AASLD, 2011http://www.infectiologie.org.tn
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HCV Viral Load as a Predictor of SVR (BOC Arms Combined)
59
27
52
26
54
26
0
20
40
60
80
100
% S
VR
1017 20
73
2752
376936
14056
213
RESPOND-2 SPRINT-2 CombinedStudies
p = 0.014 p <0.001 P<0.001
< 2.106 > 2.106 UI/ml < 2.106 > 2.106 UI/ml < 2.106 > 2.106 UI/ml
Bacon, AASLD, 2011http://www.infectiologie.org.tn
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SAFETY OF TELAPREVIR OR BOCEPREVIR IN COMBINATION WITH PEGINTERFERON
ALFA/RIBAVIRIN, IN CIRRHOTIC NON RESPONDERS FIRST RESULTS OF THE FRENCH EARLY ACCESS
PROGRAM (ANRS CO20-CUPIC)
C Hézode1, C Dorival2, F Zoulim3, T Poynard4, P Mathurin5, S Pol6, D Larrey7, P Cacoub4, V de Ledinghen8, M Bourlière9, PH Bernard10, G Riachi11, Y Barthe2, H Fontaine6, F Carrat2, JP Bronowicki12
for the CUPIC study group (ANRS CO 20)
Hôpital Henri Mondor, Créteil1, UMR-S 707, Paris2, INSERM U871, Lyon3, Hôpital de la Pitié-Salpêtrière, Paris4, Hôpital Claude Huriez, Lille5, Hôpital Cochin, Paris6, Hôpital Saint-
Eloi, Montpellier7, Hôpital Haut-Lévèque, Pessac8, Fondation Hôpital Saint Joseph, Marseille9, Hôpital Saint André, Bordeaux10, Hôpital Charles Nicolle, Rouen11, Hôpital de Brabois, Nancy12, France
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CUPIC Patients HCV genotype 1 patients
Compensated cirrhosis (Child Pugh A)
Non-responders
– Relapsers
– Partial responders
(↓ >2 log10 HCV RNA decline at Week 12)
– Null responders theoretically excluded
Treated in the French early access program
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Treatment regimen
Peg-IFN α-2a + RBVTVR + Peg-IFN α-2a + RBV Follow-up
484 160 128Weeks
72
SVR assessment
BOC + Peg-IFN α-2b + RBV Follow-upPeg-IFN + RBV
36
http://www.afssaps.fr/var/afssaps_site/storage/original/application/4b8c53711bab9d8f7d4c3f947caa90f6.pdfhttp://www.afssaps.fr/var/afssaps_site/storage/original/application/fa78af08e029caf9d82bcd9d3e77eb09.pdf
BOC: 800 mg/8h; Peg-IFNα-2b: 1.5 µg/kg/week; RBV: 800 to 1400 mg/day
TVR: 750 mg/8h; Peg-IFNα-2a: 180 µg/week; RBV: 1000 to 1200 mg/day
Interim analysis
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Patients, (% patients with >1 event) Telaprevirn=296
BoceprevirN=159
Serious adverse events (SAEs)* 48.6% 38.4%
Premature discontinuation 26.0% 23.9%
Death 2.0% 1.3%
Infection (Grade 3/4) 8.8% 2.5%
Anemia (Grade 3/4) 19.6% 22.6%
EPO use 56.8% 66.0%
Transfusion 15,2% 10.7%
Rash Grade 3Grade 4
6.8%0.7%
0%0%
Pruritus (Grade 3/4) 3.7%*407 SAEs in 144 patients; SCAR: severe cutaneous adverse reaction
Preliminary safety findings
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Telaprevir: preliminary efficacy data
0
20
40
60
80
100
Week 4 Week 8 Week 12 Week 16
53
85 86 86
% o
f pat
ient
s w
ith u
ndet
ecta
ble
HC
V R
NA
145/276 224/265 219/254 177/205
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Boceprevir: preliminary efficacy data
0
20
40
60
80
Week 4 Week 8 Week 12 Week 16
% o
f pat
ient
s w
ith u
ndet
ecta
ble
HC
V R
NA
1
37
61
71
2/155 55/149 88/144 89/126
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Practical use of boceprevir and telaprevir in France
• Indications : treatment of hepatitis C, genotype 1, in association with PR, in patients with compensated liver disease, naive or non responders to previous anti HCV treatment.
BOCEPREVIR ( VICTRELIS°) 4 capsules 200 mg x 4/d Lead-in : PegIFN+RBV
for 1 month BOC+PegIFN+RBV until
W44, or W28 (if eRVR+)
TELAPREVIR (INCIVO°) 2 capsules 750 mg, TID,
with meal Duration : 12 weeks Followed by PR until
W48 or 24 (if eRVR+)
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The future?
Combinations of direct active drugs (DADs)– High barrier of resistance– With and without interferon
Short duration of treatment : 24, 12, 8 weeks
Pangenotypic or genotype specific
Questions unresolved– Interactions – Place of ribavirin
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Novel anti HCV drugs
Pawlotsky JM. Hepatology 2011 [epub ahead of print]Zeuzem S. CCO slide set
NS3 ProteaseNS5B Polymerase
NS5A CyclophilinNucleos(t)ide(NPOL)
Non-nucleoside(NNI)
TelaprevirBoceprevirDanoprevirTMC435 BI 201335asunaprevirBMS-650032ABT-450GS-9451GS-9256MK-5172ACH-1625VX-985CTS-1027
MericitabineGS7977IDX 184
TegobuvirFilibuvirANA598BI 207127ABT-333VX-222ABT-072BMS-791325
daclatasvirBMS 824393CF102
AlisporivirSCY-465
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43/7748/81 49/80 53/78 18/46
x 3/j16+
x 3/j28+
x 3/j40+
x 2/j28+
x 3/j28-
Doses de BI-7127Durée (sem.)
RBV +/-
RVS12%
Zeuzem S, EASL 2012, Abs. 101*RVS4
Traitement without interferon in genotype 1b naive patients
60
• BI-201335 (prot inhib) + BI-207127 ( NS5B pol inhib) +/- RBV
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Gane EJ, EASL 2012, Abs. 1113
Genotypes2/3
Naive8 weeks
n (%)
Genotype 1Null
responders12 weeks
n (%)
Genotype 1Naive
12 weeksn (%)
Genotypes2/3
Non responders12 weeks
n (%)
W2 10/10 (100) 7/10 (70) 17/24 (71) 21/25 (84)
SVR4 10/10 (100) 1/9 (11) 22/25 (88) 12/15 (80)
SVR12 10/10 (100) - - -
Virologic response
ELECTRON : bitherapy GS-7977/ribavirin 49
8 weeks for GT 2/3 naive but 12 weeks not suffisant for GT1 nullresponders
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Efficacy of daclatasvir and GS-7977 +/-ribavirine in genotype 1 naive patients
Mal
ades
(%)
N = 0
20
40
60
80
100
15 15
67
14
79 67
87
100
93
100
73
100
100
100
93
93
100
100
87
87
86
86
93
93
100
100
100
100
100
100
15 1514 15 1514 15 1514 15 1514S2 S12 S24
(Fin traitement)S4 RVS4
Sulkowski M, EASL 2012, Abs. 1422
100 % (44/44) of G1 patients had an RVS W4 with the combinationDCV + GS7977
GS-7977 LI + DCV
DCV + GS-7977+ RBV
DCV + GS-7977
% < LDQ
% < LDD
69
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First generation protease inhibitors associated with pegylated interferon and ribavirin– 30% increase of SVR rate, in naive and non responders
patients
– GT1 only
– Low efficacy if cirrhosis and null responders
– Severe side effects
Future– Several new molecules with high genetic barrier
– dual or triple triple therapy with ou without RBV
– End of life for interferon in HCV disease
Conclusions
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Course of acute infection towards chronicity
Symptoms +/-
Time after Exposure
Tite
ranti-HCV
ALT
Normal
0 1 2 3 4 5 6 1 2 3 4YearsMonths
HCV RNA
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Patients, n (% patients with at least one event)
Telaprevir n=296
Serious adverse events (SAEs)* 144 (48.6%)
Premature discontinuationDue to SAEs
77 (26.0%)43 (14.5%)
DeathSepticemia, Septic shock, Pneumopathy, Oesophageal varices Bleeding, Encephalopathy, Lung carcinoma
6 (2.0%)
Infection (Grade 3/4) 26 (8.8%)
Asthenia (Grade 3/4) 14 (4.7%)
RashGrade 3Grade 4 (SCAR)
20 (6.8%)2 (0.7%)
Pruritus (Grade 3/4) 11 (3.7%)
Hepatic decompensation (Grade 3/4) 13 (4.4%)*407 SAEs in 144 patients; SCAR: severe cutaneous adverse reaction
Telaprevir: preliminary safety findings
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Patients, n (% patients with at least one event) Telaprevir (n=296)
AnemiaGrade 2 (8.0 – <10.0 g/dL)Grade 3/4 (<8,0 g/dL)EPO useBlood transfusion
58 (19.6%)30 (10.1%)
168 (56.8%)45 (15.2%)
NeutropeniaGrade 3 (500 – <1000/mm3)Grade 4 (<500/mm3)G-CSF use
12 (4.0%)2 (0.7%)7 (2.4%)
Thrombopenia Grade 3 (25 000 – <50 000)Grade 4 (<25 000)Thrombopoïetin Use
35 (11.8%)4 (1.3%)5 (1.7%)EPO: érythropoïétine; G-CSF: granulocyte-colony stimulating factor
Telaprevir: preliminary safety findings
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Patients, n (% patients with at least one event) Boceprevir (n=159)
Serious adverse events (SAEs)* 61 (38.4%)
Premature discontinuationDue to SAE
38 (23.9%)12 (7.4%)
DeathBronchopulmonary infection, Sepsis 2 (1.3%)Infection (Grade 3/4) 4 (2.5%)
Asthenia (Grade 3/4) 9 (5.7%)
RashGrade 3Grade 4 (SCAR)
00
Pruritus (Grade 3/4) 1 (0.6%)
Hepatic decompensation (Grade 3/4) 7 (4.4%)
*158 SAEs in 61 patients; SCAR: severe cutaneous adverse reaction
Boceprevir: preliminary safety findings
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Patients, n (% patients with at least one event) Boceprevir (n=159)
AnemiaGrade 2 (8.0 – <10.0 g/dL)Grade 3/4 (<8,0 g/dL)EPO useBlood transfusion
36 (22.6%)16 (10.1%)
105 (66.0%)17 (10.7%)
NeutropeniaGrade 3 (500 – <1000/mm3)Grade 4 (<500/mm3)G-CSF use
7 (4.4%)1 (0.6%)6 (3.8%)
Thrombopenia Grade 3 (25 000 – <50 000)Grade 4 (<25 000)Thrombopoïetin Use
10 (6.3%)1 (0.6%)3 (1.9%)
EPO: érythropoïétine; G-CSF: granulocyte-colony stimulating factor
Boceprevir: preliminary safety findings
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Main classes of anti HCV inhibitors
Protease inhibitors
– 1st generation and approved: telaprevir, boceprevir
– 2nd generation
Polymerase inhibitors– Nucleosidic inhibitors
– Non nucleosidic inhibitors
NS5A inhibitors
Entry inhibitors
Immunomodulators
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