giorgio arcangeli highlights in the management of urogenital cancer rome may 9-10, 2008 radiation...
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Giorgio Arcangeli
Highlights in the Management Highlights in the Management of Urogenital Cancerof Urogenital Cancer
Rome May 9-10, 2008Rome May 9-10, 2008
Radiation Therapy is the bestRadiation Therapy is the best
treatment approach for treatment approach for
localized prostate cancerlocalized prostate cancer
Radiation Therapy is the bestRadiation Therapy is the best
treatment approach for treatment approach for
localized prostate cancerlocalized prostate cancer
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CARCINOMA OF THE PROSTATE
risk to treat scarcely aggressive
indolent tumors
risk to treat scarcely aggressive
indolent tumors
multiple therapeutic options
multiple therapeutic options
High probabilityof cure in
localized tumors
High probabilityof cure in
localized tumors
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CRITERIA FOR TREATMENT CHOICE
TUMOR RELATED (Stage - G.S. - PSA)
PATIENT RELATED (age - P.S.)
TREATMENT RELATED (Acute and late side effects, QOL)
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Clinical Staging of prostate cancer
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Clinical Staging of prostate cancer
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Clinical Staging of prostate cancer
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Clinical Staging of prostate cancer
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SISTEMA DI GLEASON (1974) SISTEMA DI GLEASON MODIFICATO (ISUP 2005)
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CARCINOMA OF THE PROSTATADefinitive treatment options in localized tumors
HIGH DOSE RADIOTHERAPY±
ANDROGEN DEPRIV.
HIGH DOSE RADIOTHERAPY±
ANDROGEN DEPRIV.
RADICALPROSTATECTOMY
RADICALPROSTATECTOMY
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0
500
1000
1500
2000
2500
3000
3500
84 85 86 87 88 89 90 91
SurgeryRadiotherapy
AGE < 70 years
(Harlan: J Clin Oncol, 1995)YEARS OF DIAGNOSIS
CARCINOMA OF THE PROSTATE
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0
500
1000
1500
2000
2500
3000
84 85 86 87 88 89 90 91
SurgeryRadiotherapy
YEARS OF DIAGNOSI(Harlan: J Clin Oncol, 1995)
AGE > 70 anni
CARCINOMA OF THE PROSTATE
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A Multi-institutional* Pooled Analysis of Radiation Therapy For Clinically Localized Prostate Cancer
(Shipley, JAMA 281:1598, 1999)
* Fox Chase; Mass General; Michigan University; Washington University; EVMS; Stanford
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ACR Patterns of Care Study :Risk of Grade 3-4 Complications by Radiation
Dose in Carcinoma of the Prostate
Dose # Patients % Complications
<70 Gy 428 3.5%
>70 Gy 174 6.9%
p = 0.03
Modified from Leibel SA, Hanks GE, Kramer S. IJROBP, 10, 401, 1984
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120100806040200
20
40
60
80
100
Prescription Dose
Pro
bab
ility
(%
)
Shifting The Organ Toxicity Curveby Decreasing the Irradiated Volume
TumorControl Organ
Toxicity
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Multileaf Collimator for Conformal or Intensity Modulater Radiation Therapy
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Dynamic Multileaf ( “Sliding window”)• le lamelle si muovono in modo continuo ed unidirezionale durante l’erogazione, sempre da sinistra verso destra, fino ad una velocità di 2.5 cm/s;
• ogni lamella si sposta a velocità diversa dalle altre, ricongiungendosi alla lamella opposta nella posizione finale;
• l’erogazione è continua durante il movimento delle lamelle.
Fluence Matrix
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Why IMRT ???• Creation of concave or convex isodose surfaces with
sharp dose gradients• Higher dose to target volume• Specific sparing of sensitive volumes (organs at risk)
within complex treatment geometries
With IMRT dose distribution can be shaped to the target to spare Organs at Risk
Beam Profile #1 1
Beam Profile # 2
Beam
Profile #3
Dose Intensity
PTV
RORO
PTV
3-field IMRT
Prescribed Dose (typical distribution)
3-field RT
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Isodose comparison betwen CRT or IMRT 20-30%40-50%60-70%80-90%90-100%>100%
20-30%40-50%60-70%80-90%90-100%>100%
Dose prescription: 80 Gy to isocentre, 2 Gy per fractions, 5 fr/week
6 FIELDS-3DCRT 5 FIELDS-IMRT
bladdder6 fields-3DCRT
5 fields-IMRT
PTVrectum
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Per
cen
t G
rad
e 2
Rec
tal
Ble
edin
g
0 12 24 36 48 60 72 84 96 108
Time (months)
0
5
10
15
20
6480 cGy (96)
7020 cGy (268)
7560 cGy (446)
8100 cGy (61)
Zelefsky 1999
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Pe
rce
nt
≥ G
rad
e 2
GI T
ox
icit
y
0 12 24 36 48 60 72 84 96
Months
5
10
15
20
p< 0.001
81 Gy IMRT (171)
81 Gy Conventional 3D-CRT (61)
0
Zelefsky 2001
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Dose escalationwith External BeamRadiation Therapy
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Biochemical Failure-Free
Zietman AL, JAMA 2005
All Pts. Intermediate to high risk
Low risk70.2 Gy vs 79.2 Gy
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Peeters STH et al. JCO 2006
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Conventional vs. High dose 3D-CRT in pts with prostate cancer receiving 3-6 mos NCADT
Randomized phase III study (MRC RT01)
74 Gy
64 Gy
HR=0.67(0.53-0.85)P=0.0007
Dearnaley, Lancet Oncol 2007
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External Beam Radiation Therapy
VsRadical Prostatectomy
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bNed for surgically and radiation-managed patients stratified into risk groups
low risk
intermediaterisk
high risk
D’Amico A, IJROBP 1997
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bRFS in pts with favorable tumors (T1-T2A, bGS< 6, iPSA< 10 ng/ml)
Kupelian PA, JCO 2002
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bRFS in pts with unfavorable tumors (T2b-T2c, bGS> 6, iPSA>10 ng/ml)
Kupelian PA, JCO 2002
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Akakura K, Jpn J Clin Oncol 2006
bNED OS
P=0.25 P=0.30
RP: 46 pts – EBRT (60-70 Gy): 49 pts (2 month neoadjuv DES 300mg and adjuv LHRH until progress)
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Characteristics of Pts with high risk prostate cancer
Variable RP EBRT p-value
Median Age 65.5 75.0 <0.001bGS < 6 29 (24%) 17 (10%) 7 82 (67%) 105 (65%) <0.001 > 8 11 (9%) 40 (25%)cT-Stage <T2c 110 (90%) 70 (43%) T2c 4 (3%) 71 (48%) <0.001 >T2c 8 (7%) 21 (9%)iPSA <10 2 (1%) 44 (27%) 11-20 57 (47%) 55 (34%) <0.001 >20 63 (52%) 63 (39%)Median FU 30.5 mos 30.7 mos 0.56
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EAU Guidlines for follow-up after treatment with curative intent
•After RP a serum PSA level > 0.2 can be associated with residual or recurrent disease (grade B recommendation)
•After EBRT a rising PSA level 2.0 ng/ml above the nadir value, rather than a specific threshold value, is the most reliable sign of persistent or recurrent disease (grade B recommendation)
•Both a palpable nodule and rising PSA level can be signs of local disease recurrence (grade B recommendation)
Eur Urology 2008
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p=n.s. p=n.s. p=n.s.(238 pts.)
(46 pts.) (238 pts.)(104 pts.)(180 pts.) (46 pts.)
FFBF in high risk prostate tumors according to different scores of clinical prognostic factors
IRE Apr 2008
bGS iPSAcT-stage
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(123 pts.)
(159 pts.)
FFBF as a function of Age in pts with high risk prostate cancer treated with RP or EBRT
IRE Apr 2008
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p = 0,0012
(162 pts.)
(122 pts.)
FFBF after RP or EBRT in pts with high risk prostate cancer
IRE Apr 2008
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RP
p=n.s.= 0.06p=n.s
EBRT
p=0.005p=n.s.
FFBF according to bGS ± 8 and iPSA ± 20 ng for RP and EBRT
(11 pts)
(111 pts)
(40 pts)
(122 pts)
(63 pts)
(59 pts)
(63 pts)
(99 pts)
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p = 0.0161
FFBF of Pts with worst prognosis according to the treatment received
IRE Apr 2008
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(152pts.)
(10pts.)
p= 0.001
FFBF according to nPSA in Pts treated with EBRT
IRE Apr 2008
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p=0.62
p=0.06
p=0.0001(162 pts.)
(83pts.)
(39 pts.)
FFBF of Pts treated with EBRT, RP only or RP + Adjuvant Treatment
IRE Apr 2008
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p=n.s.
p=n.s.
p=0.008
p=n.s.
FFBF according to different scores of pathologic factors
(88 pts)(23 pts)
(17 pts)
(96 pts)
(25 pts)
(71 pts)
(8 pts)
(103 pts)
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Univariate analysis of RP patient
Variable 3-yr FFBF rate p-value
bGS (≥8 vs <8) 72% vs 77% 0.74
cT (>T2c vs <T2c) 37% vs 77% 0.08
iPSA (>20 vs < 20) 68% vs 81% 0.06
SM+ vs SM- 79% vs 72% 0.73
pGS (>8 vs <8) 53% vs 81% 0.008
pN+ vs pN- 60% vs 73% 0.53
pT (>T2c vs <T2c) 72% vs 78% 0.74
Adjuv Treatm (Y vs N) 65% vs 87% 0.06
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Univariate analysis of EBRT patient
Variable 3-yr FFBF rate p-value
bGS (>8 vs <8) 77% vs 93% 0.005
cT (>T2c vs <T2c) 83% vs 93% 0.66
iPSA (>20 vs < 20) 86% vs 91% 0.26
nPSA (>0.5 vs <0.5) 40% vs 94% 0. 001
Fractionation
(standard vs hypo) 76% vs 96% 0.06
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Univariate analysis of all patients
Variable 3-yr FFBF rate p-value
bGS (> 8 vs < 8) 73% vs 85% 0.17
cT (>T2c vs <T2c) 74% vs 83% 0.82
iPSA (>20 vs < 20) 76% vs 81% 0.01
Age (>70 vs <70) 84% vs 80% 0. 61
Treatment
(RP vs EBRT) 80% vs 92% 0.001
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Summary of Multivariate Analysis
Group Variable p-value
RP pGS (<7 vs =7 vs >7) 0.04
EBRT nPSA (continuous) 0.0002
All PTS iPSA (continuous) 0.01
Treatment (RP vs EBRT) 0.007
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Rectal and urinary late toxicity
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Incidence of grade >2 late toxicity
rectal
urinary
convent
convent
hypo
hypo
IRE, Oct 2007
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Radiation Proctitis Related Factors
Radiation related factors•Total dose•Dose per fraction•Dose/volume relationship•PTV size•RT technique•N° of RT fields•Rectal motion
Patient related factors•Previous history of proctitis•Previous abdominal surgery•Cardiovascular disease•Arterial hypertension•Peripheral vascular disease•Diabetes•Hemorrhoids•Prostate size•Long term ADT
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99
Non confluent multipleTelangectasia
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Freedom from rectal toxicity as a function of rectal volume receiving > 70 Gy (V70)
Pollack IJROBP 2002
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Disfunzione erettile
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Sexual potency preservation
– Radiotherapy: 73%
– Radiotherapy (high doses): 61%
– Radiotherapy + neoadiuv ADT: 79%
– Radioterapia + adiuvant ADT: 0%
Pilepich 1999, D’Amico&Zelefsky ASTRO2004
Radiation mediated impotence is multifactorial. Of pts. evaluated for impotence, 63% had arteriogenetic dysfunction, 31% cavernosal dysfunction, and only 3% had a neurogenic impotence
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Merrick GS ASTRO 2004
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Merrick GS ASTRO 2004
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Tsai HK, JNCI 2007
EBRT, age≥65 yrEBRT, age<65 yr
RP, age<65 yr RP, age≥65 yr
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Quality of life-Prospective evaluation-Patient/Physician evaluation-Validated instruments
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Litwin Cancer 007
BrachytherapyEBRTRP
BrachytherapyEBRTRP
Actuarial analysis of the subjects returned to baseline HRQOL scores
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Litwin Cancer 2007
All Pts
Pts initiallypotent
Actuarial analysisof the subjects returned to baseline sexual scores
BrachytherapyEBRTRP
BrachytherapyEBRTRP nerve-sparingRP non nerve-spar
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Grazie per la VostraGrazie per la VostraAttenzione!Attenzione!
Grazie per la VostraGrazie per la VostraAttenzione!Attenzione!
Ringrazio:
Pr. M Gallucci, Dr. P De Carli, Dr. R Papalia (Div. Urologia), Dr. L Strigari, Dr V Landoni, Pr. M Benassi (Lab Fisica Medica) e i miei collaboratori della SC Radioterapia: Dr. B Saracino, Dr. MG Petrongari M, Dr. S Gomellini, Dr. S Arcangeli.