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Systemic treatment of advanced testicular cancer Karim Fizazi, MD, PhD Institut Gustave Roussy, France
Metastatic GCT: Prognosis (IGCCC) Good prognosis Intermediate prognosis Poor prognosis J Clin Oncol 1997, 15: 594-603
Stage II seminoma ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Séminome testiculaire stade IIA/B: Résultats de la radiothérapie ,[object Object],Etude prospective; suivi: 6 ans No. pts: 87;  IIA: 66;  IIB: 21 4 rechutes: médiastin ± métas: 3; iliaque controlatéral: 1 Taux de rechute: IIA:  4.7% IIB: 11.1% Ces 4 rechutes ont été rattrapées par chimiothérapie Disease-specific survival: 100%
Chemotherapy for metastatic seminoma ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
GETUG S99 study ,[object Object],[object Object],[object Object],[object Object]
Séminomes métastatiques Bon pronostic Pronostic intermédiaire Pas de M+ visc extra-P LDH < 2N si supra-diaph M+ viscérales extra-P ou LDH > 2N si supra-diaph 4 EP 4 VIP + G-CSF IGCCCG MRC
Progression-free survival: 3-year PFS:  91%  (84-95) 5-year PFS:  85%  (76-91) Overall survival: 3-year OS:  96%  (91-99) 5-year OS:  92 %  (83-96) ,[object Object],[object Object],[object Object],[object Object],[object Object],GETUG S99 study in metastatic seminoma
Survival according to prognosis Progression-free survival (3-year): Good prognosis group:  93%  (85-97) Intermediate prognosis group:  83%  (63-93) Overall survival (3-year): Good prognosis group:  99%  (92-100) Intermediate prognosis group:  87%  (67-95) Fizazi K et al., ASCO 2009
Séminomes avancés: Masses résiduelles post-chimiothérapie ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
TEP for residual masses after chemotherapy for metastatic seminoma ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],De Santis, J Clin Oncol 2004, 22: 1034-1039
Vers une décroissance thérapeutique? ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Proposition étude française Séminome stade II (A-C?) 2 cycles d’EP Pet-scan Si - 1 cycle carbo Si + 2 cycles EP
Treatment for metastatic  non-seminomatous germ-cell tumors (NSGCT)
Principles of treatment for metastatic NSGCT ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
The BEP regimen ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Good  prognosis metastatic NSGCT ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],J Clin Oncol 1997, 15: 594-603
Good prognosis metastatic NSGCT ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Logrank p=0.06 n= 251 Good-risk NSGCT Event-Free Survival GETUG T93 trial:  3 BEP vs 4 EP Culine et al., Ann Oncol 2007 0,5 0,6 0,7 0,8 0,9 1,0 0 2 4 6 8 YEARS PROBABILITY 4EP; 84% at 4 years 3BEP; 90% at 4 years
GETUG T93 trial:  3 BEP vs 4 EP Logrank p=0.14 BEP: 5 deaths EP: 12 deaths Median follow-up = 51 months Culine et al., Ann Oncol 2007 Overall Survival
Poor  prognosis metastatic NSGCT ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],J Clin Oncol 1997, 15: 594-603
A standard established in 1987… ,[object Object],[object Object],[object Object],[object Object],4 BEP= standard
4 BEP are not 5, 6, or 7… ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Giving > 4 BEP makes your patient at a 2% risk of meeting this: ,[object Object],[object Object],[object Object],Kollmansberger, J Clin Oncol 1998, 16: 3386-91
Time to treatment failure Overall survival Phase III intergroup US trial  Intermediate/poor risk pts n= 219 2 BEP + 2 HDCT   (CBDCA, VP16, CPM) Motzer, J Clin Oncol 2007; 25: 247-256 4 BEP R
Poor prognosis NSGCT: Randomized trials  Courtesy of S. Culine   Chemotherapy   Number of patients    Favorable  response rates (%)     Conclusion   Reference BEP x 4 v BEP 200  x 4 78   81 73   68 Double dose cisplatin not superior  and more toxic   Nichols 1991 BEP x 4 v BEP/PVB x 4 125   125 76   72 Alternating regimen not superior  and more toxic   de Wit 1995 BEP x 4/EP x 2 v BOP/VIP-B 190   190 57   54 Dose dense alternating regimen  not superior and more toxic    Kaye 1998 BEP x 4 v VIP x 4 148   151 60   63 Substitution of ifosfamide  for bleomycin not superior and more toxic   Nichols 1998 P 200 VBE x ¾ v P 200 VBE x 2 + P 200 EC 58   57 75   67 High dose chemotherapy not superior  and more toxic   Droz 2007 BEP x 4 v BEP x 3 + CaEC 111   108 55   56 High dose chemotherapy  not superior  and more toxic   Motzer 2007 BEP x 4 v CISCA/VB 96   94 61   54 Alternating regimen not superior  and more toxic   Culine 2008
Poor prognosis NSGCT:  where do we stand? ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Management of pts at high risk of ARDS: « Very high risk NSGCT » Massard, Ann Oncol 2010 ,[object Object],[object Object],8/25 4/10 ( 40% ) 4/15 ( 27% ) Long-term survivor 12/25 2/10 10/15 Death from ARDS 16/25 3/10 ( 30% ) 13/15 ( 87% ) ARDS Total 1997-2006 1980-1997
Overall survival according to  tumor marker decline at day 21 or day 42 TM assessed at Day 21 Fizazi, J Clin Oncol 2004, 22: 3868-76 Motzer, J Clin Oncol 2007; 25: 247-256 TM assessed at Day 42
GETUG 13 trial ,[object Object],[object Object],[object Object],[object Object]
GETUG 13:  dose-dense regimen BEP x 1 Taxol-BEP + Oxaliplatin  (d10) + G-CSF / 3 weeks x 2 cycles Cisplatin, Ifosfamide, bleomycine  + G-CSF / 3 weeks x 2 cycles
Is the number of treated cases important for outcome? ,[object Object],[object Object],[object Object],[object Object],[object Object],Collette L et al. J Natl Cancer Inst 1999;91:839-846
Kaplan-Meier estimate of failure-free survival according to total accrual of patients by the treating institution in trial 30895/TE13. Collette L et al. JNCI J Natl Cancer Inst 1999;91:839-846 Oxford University Press Failure-Free Survival
Kaplan-Meier estimate of overall survival according to the total accrual of patients by the treating institution in trial 30895/TE13. Collette L et al. JNCI J Natl Cancer Inst 1999;91:839-846 Oxford University Press Overall survival
Salvage chemotherapy Stage I Survival 99% Metastatic stages (IGCCCG) ,[object Object],[object Object],[object Object],Salvage setting post-first-line CT 95% 80% 50% 25%
Salvage treatment for patients failing first-line chemotherapy ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Prognostic classification: metastatic GCT + failure to first-line cisplatin-based chemotherapy J Clin Oncol 2010, 28: 4906-11 ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],PFS n= 1984 pts
HD chemotherapy for 2 nd  line:  IT94 phase III trial n= 280 1994-2001
IT94: Overall survival Pico et al., Ann Oncol 2005, 16: 1152-1159 Conclusion: No demonstrated benefit for single HD chemotherapy
Single vs Sequential  HD chemotherapy for salvage Lorch A et al., J Clin Oncol 2007, 25: 2778-84 n= 230 pts 1 VIP + 3 HD CE 3 VIP + 1 HD CEC R Accrual stopped for tox (B) No difference in outcome Sequential CT better tolerated OS PFS EFS
Conclusion: Metastatic GCT ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]

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ECCLU 2011 - K. Fizazi - Testicular cancer - Treatment of advanced testicular cancer

  • 1. Systemic treatment of advanced testicular cancer Karim Fizazi, MD, PhD Institut Gustave Roussy, France
  • 2. Metastatic GCT: Prognosis (IGCCC) Good prognosis Intermediate prognosis Poor prognosis J Clin Oncol 1997, 15: 594-603
  • 3.
  • 4.
  • 5.
  • 6.
  • 7. Séminomes métastatiques Bon pronostic Pronostic intermédiaire Pas de M+ visc extra-P LDH < 2N si supra-diaph M+ viscérales extra-P ou LDH > 2N si supra-diaph 4 EP 4 VIP + G-CSF IGCCCG MRC
  • 8.
  • 9. Survival according to prognosis Progression-free survival (3-year): Good prognosis group: 93% (85-97) Intermediate prognosis group: 83% (63-93) Overall survival (3-year): Good prognosis group: 99% (92-100) Intermediate prognosis group: 87% (67-95) Fizazi K et al., ASCO 2009
  • 10.
  • 11.
  • 12.
  • 13. Proposition étude française Séminome stade II (A-C?) 2 cycles d’EP Pet-scan Si - 1 cycle carbo Si + 2 cycles EP
  • 14. Treatment for metastatic non-seminomatous germ-cell tumors (NSGCT)
  • 15.
  • 16.
  • 17.
  • 18.
  • 19. Logrank p=0.06 n= 251 Good-risk NSGCT Event-Free Survival GETUG T93 trial: 3 BEP vs 4 EP Culine et al., Ann Oncol 2007 0,5 0,6 0,7 0,8 0,9 1,0 0 2 4 6 8 YEARS PROBABILITY 4EP; 84% at 4 years 3BEP; 90% at 4 years
  • 20. GETUG T93 trial: 3 BEP vs 4 EP Logrank p=0.14 BEP: 5 deaths EP: 12 deaths Median follow-up = 51 months Culine et al., Ann Oncol 2007 Overall Survival
  • 21.
  • 22.
  • 23.
  • 24.
  • 25. Time to treatment failure Overall survival Phase III intergroup US trial Intermediate/poor risk pts n= 219 2 BEP + 2 HDCT (CBDCA, VP16, CPM) Motzer, J Clin Oncol 2007; 25: 247-256 4 BEP R
  • 26. Poor prognosis NSGCT: Randomized trials Courtesy of S. Culine   Chemotherapy   Number of patients   Favorable response rates (%)     Conclusion   Reference BEP x 4 v BEP 200 x 4 78   81 73   68 Double dose cisplatin not superior and more toxic   Nichols 1991 BEP x 4 v BEP/PVB x 4 125   125 76   72 Alternating regimen not superior and more toxic   de Wit 1995 BEP x 4/EP x 2 v BOP/VIP-B 190   190 57   54 Dose dense alternating regimen not superior and more toxic   Kaye 1998 BEP x 4 v VIP x 4 148   151 60   63 Substitution of ifosfamide for bleomycin not superior and more toxic   Nichols 1998 P 200 VBE x ¾ v P 200 VBE x 2 + P 200 EC 58   57 75   67 High dose chemotherapy not superior and more toxic   Droz 2007 BEP x 4 v BEP x 3 + CaEC 111   108 55   56 High dose chemotherapy not superior and more toxic   Motzer 2007 BEP x 4 v CISCA/VB 96   94 61   54 Alternating regimen not superior and more toxic   Culine 2008
  • 27.
  • 28.
  • 29. Overall survival according to tumor marker decline at day 21 or day 42 TM assessed at Day 21 Fizazi, J Clin Oncol 2004, 22: 3868-76 Motzer, J Clin Oncol 2007; 25: 247-256 TM assessed at Day 42
  • 30.
  • 31. GETUG 13: dose-dense regimen BEP x 1 Taxol-BEP + Oxaliplatin (d10) + G-CSF / 3 weeks x 2 cycles Cisplatin, Ifosfamide, bleomycine + G-CSF / 3 weeks x 2 cycles
  • 32.
  • 33. Kaplan-Meier estimate of failure-free survival according to total accrual of patients by the treating institution in trial 30895/TE13. Collette L et al. JNCI J Natl Cancer Inst 1999;91:839-846 Oxford University Press Failure-Free Survival
  • 34. Kaplan-Meier estimate of overall survival according to the total accrual of patients by the treating institution in trial 30895/TE13. Collette L et al. JNCI J Natl Cancer Inst 1999;91:839-846 Oxford University Press Overall survival
  • 35.
  • 36.
  • 37.
  • 38. HD chemotherapy for 2 nd line: IT94 phase III trial n= 280 1994-2001
  • 39. IT94: Overall survival Pico et al., Ann Oncol 2005, 16: 1152-1159 Conclusion: No demonstrated benefit for single HD chemotherapy
  • 40. Single vs Sequential HD chemotherapy for salvage Lorch A et al., J Clin Oncol 2007, 25: 2778-84 n= 230 pts 1 VIP + 3 HD CE 3 VIP + 1 HD CEC R Accrual stopped for tox (B) No difference in outcome Sequential CT better tolerated OS PFS EFS
  • 41.

Hinweis der Redaktion

  1. Kaplan-Meier estimate of failure-free survival according to total accrual of patients by the treating institution in trial 30895/TE13. O = number of events; N = number of patients in each group. Two-sided P = .018 in stratified analysis; hazard ratio of institutions that entered fewer than five patients versus institutions that entered five patients or more = 1.56 (95% confidence interval = 1.09-2.27). The 1-year failure-free survival rate was 43% (95% confidence interval = 29%-56%) in the institutions that entered fewer than five patients and 59% (95% confidence interval = 54%-65%) in those that entered five patients or more. At 2 years, the failure-free survival rates were 38% (95% confidence interval = 25%-51%) and 55% (95% confidence interval = 50%-61%) in the two groups of institutions, respectively.
  2. Kaplan-Meier estimate of overall survival according to the total accrual of patients by the treating institution in trial 30895/TE13. O = number of deaths; N = number of patients in each group. Two-sided P = .010 in stratified analysis; hazard ratio of institutions that entered fewer than five patients versus institutions that entered five patients or more = 1.85 (95% confidence interval = 1.16-3.03). The 1-year survival rate was 70% (95% CI = 57%-82%) in the group that entered fewer than five patients and 82% (95% confidence interval = 78%-87%) in the group with at least five patients. The 2-year survival rates were 62% (95% confidence interval = 48%-75%) and 77% (95% confidence interval = 72%-81%) in the two groups of institutions, respectively.