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Medical treatment of  pancreatic cancer UVSQ University  of Versailles Saint Quentin  en yveline Philippe Rougier Digestive Oncology Hopital Européen Georges Pompidou 75015 Paris ; France [email_address] Pancreas: A complex anatomy
Pancreatic cancer: a major  therapeutic challenge ,[object Object],[object Object],[object Object],[object Object],1 Burris H, et al.  J Clin Oncol  1997;15:2403 – 13
Medical treatment of metastatic pancreatic cancer ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
1997: Gemcitabine became a standard of care in advanced pancreatic cancer 0 2 4 6 8 10 12 14 16 18 20 100 80 60 40 20 0 Weekly b 5-FU Weekly Gemcitabine Survival time (months) Patients surviving (%) 1 Burris H, et al.  J Clin Oncol  1997;15:2403 – 13 Gemcitabine 5-FU p Median survival (mo) 5.65 4.41 0.0025 Clinical benefit (%) 23.8 4.8 0.0022 1-year survival (%) 18 2
Heinemann V, BMC Cancer 2008  Platin salts Fluoropyrimidines Autres in favor of Gem + X in favor of Gem alone Meta-analysis: combinations in first line Not done on individal data G + Platinum salts G + FU derivatives
Medical treatment of metastatic pancreatic cancer ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
PRODIGE 4 / Accord 11 trial  Phase III : Gemzar  vs  Folfirinox ,[object Object],GEMZAR (Burris) FOLFIRINOX* primary endpoint :  OS Gain : 7 to 10 months ADK pancreas M+ N = 342 Stratification : center PS : 0 vs 1 head vs other localisation 6 months of chemotherapy recommended CTscan  every 2 months In each arm : R *  Folfirinox : d1 = d14 - Oxaliplatin 85mg/m 2  d1 - Irinotecan 180mg/m 2  d1 - folinic acid 400mg/m 2  d1 - 5FU 2400 mg/m 2  / d1-2
Disease characteristics T. Conroy  et al .,  ASCO 2010, A 4010 ; N Engl J Med 2011 in press Characteristic Folfirinox N=171 Gemcitabine N=171 p Synchronous metastases Metachronous metastases 156 (91.2%) 15  (8.8%) 161 (94.2%) 10 (5.8%) NS NS Median  nr.  of T sites CA19-9    59 ULN 2 (1-6) 68 (41.5%) 2 (1-6) 77 (46.7%) NS NS Measurable site Liver Pancreas Nodes Lungs Peritoneal 149 (88.2%) 89 (52.7%) 48 (28.4%) 33 (19.5%) 33 (19.5%) 150 (87.7%) 91 (53.2%) 39 (22.8%) 49 (28.7%) 32 (18.7%) NS NS NS 0.049 NS
Safety: hematological adverse events (Aes) 5.4 42.5% of the pts received G-CSF in the F arm vs 5.3% in the G arm One toxic death occurred in each arm T. Conroy  et al .,  ASCO 2010, A 4010 ; N Engl J Med 2011 in press AE, % per patient Folfirinox N=167 Gemcitabine N=169 p All Grade 3/4 All Grade 3/4 Grade 3/4 Neutropenia 79.9 45.7 54.8 18.7 0.0001 Febrile Neutropenia 7.2 2.4 0.6 0.009 Anemia 90.4 7.8 94.6 5.4 NS Thrombocytopen. 75.2 9.1 54.8 2.4 0.008
Objective Response Rate T. Conroy  et al .,  ASCO 2010, A 4010 ; N Engl J Med 2011 in press Folfirinox N=171 Gemcitabine N=171 p Complete response 0.6% 0% Partial response 31% 9.4% 0.0001 CR/PR 95% CI [24.7-39.1] [5.9-15.4] Stable disease 38.6% 41.5% Disease control CR+PR+SD 70.2% 50.9% 0.0003 Progression 15.2% 34.5% Not assessed 14.6% 14.6% Median duration of response 5.9 mo. 4 mo. ns
Progression-Free Survival Median PFS Folfirinox: 6.4 mo.   Median PFS Gemcitabine: 3.3 mo HR (95% CI): 0.47 (0.37-0.59) ; p < 0.0001 T. Conroy  et al .,  ASCO 2010, A 4010 ; N Engl J Med 2011 in press
Overall Survival T. Conroy  et al .,  ASCO 2010, A 4010 ; N Engl J Med 2011 in press Median survival [CI 95%]:  11.1 mo .[ 9 - 13.1] vs  6.8 mo .[ 5.5 - 7.6] P = <0.0001 ; HR =  0.57 [0.45 – 0.73]
Time to definitive QoL degradation  T. Conroy  et al .,  ASCO 2010, A 4010 ; N Engl J Med 2011 in press
Conclusions ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],T. Conroy  et al .,  ASCO 2010, A 4010 ; N Engl J Med 2011 in press
Medical treatment of metastatic pancreatic cancer ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Combining gemcitabine with  biological therapies ,[object Object],[object Object],[object Object],[object Object],[object Object]
PA.3: Overall Survival in  metastatic pancreatic cancer 1.00 0.75 0.50 0.25 0 0 6 12 18 24 30 36 Time (months) Gemcitabine + Tarceva Gemcitabine + placebo Survival probability HR=0.80 (0.66–0.98); p=0.029  Led to EU approval for the treatment of metastatic pancreatic cancer ,[object Object],[object Object],Moore, JCO 2007 Gemcitabine + Tarceva Gemcitabine + placebo n 200 197 Median survival, months 5.93 5.06
Conatumumab / AMG 479, phase II in Metastatic Pancreatic Cancer …  phase III in progress Patients à risque H. L. Kindler  et al ., ASCO 2010, A 4035  Trend in favor of anti IGFR efficacy ? Events Median OS (95% CI), mthis HR (95% CI) a p Conatumumab + gemcitabine 32 (78%) 7.5  (4.8, 10.0) 0.87  (0.53, 1.43) 0.59 AMG 479 + gemcitabine 29 (69%) 8.7  (5.3, 12.2) 0.67  (0.41, 1.12) 0.12 Placebo + gemcitabine 34 (81%) 5.9  (4.1, 9.7) 41 39 38 33 29 25 23 23 19 14 14 11 7 5 3 1 0 0 0 0 0 0 0 0 0 42 39 37 34 30 28 22 21 20 17 17 15 13 8 6 6 4 3 3 3 2 1 1 1 0 42 39 38 30 26 20 19 16 15 14 13 12 6 3 2 2 1 1 1 1 0 0 0 0 0 0.0 0.2 0.4 0.6 0.8 1.0 Survie globale 0 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 Mois
Pancreatic cancer: recent progress ? ,[object Object],[object Object],[object Object],[object Object],[object Object]
Clinical trials investigating second-line chemotherapy in gemcitabine-pretreated pts with advanced pancreatic cancer c c Treatment regimen No. of patients KPS 90-100% / ECOG 0-1 Metastatic disease (%) RR (%) DCR (%) PFS/TTP (months) OS (months) Oxa/5-FU CI/LV vs BSC 46 NA NA NA NA OFF:5.25 BSC:2.5 OFF:10 BSC:8.5 Oxa/5-FU CI/LV vs 5-FU CI/LV (nb = 168)  OFF:77  FF:  91 OFF:54% FF:  50 % OFF:85.5 FF:  89.2 NA NA OFF:3.25 FF:  2.25 OFF:6.5 FF:  3.25 Oxa/5-FU CI/LV 30 33 % 97 23 53 5.1 5.8 FOLFOX-4 42 62 % 83 14 52 4 6.7 Modified FOLFOX 30 97 % NA NA 20 1.4 4 vs modified FOLFIRI 30 100 % 28 1.9 4 Oxa + Gem 33 88 % 64 21 58 4.2 6.0 Oxa + Cap 39 80 % NA 3 23 NA 5.8 Oxa + irinotecan 30 30 % 100 10 33 4.1 5.9 Oxa + raltitrexed 41 61 % 100 24 51 1.8 5.2 Cisplatin + irinotecan + Gem + 5-FU + LV 34 NA 100 24 44 3.9 10.3 Cap + Gem + docetaxel 35 52 100 29 60 NA 11.2
5FU- Folinic-Ac (FF) Oxaliplatin-5FU- Folinic-Ac (OFF) non resecable Cancer (Localy avanced or Metastatic) Progression under Gem Karnowsky >60 n=165 Pelzer et al, ASCO 2008  A 4508 FF : 5FU 2000 mg/m²/24h, ac. folinic 200 mg/m² in 30 mn D1- D 8- D 15- D 22 OFF : FF + Oxaliplatin 85 mg/m²  D 8- D 22  D 1= D 43 Primary endpoint : Overall Survival Second line chemotherapy: CONKO-3 trial R Per protocol FF  OFF  p PFS  (weeks) 9 13 0.012 Overall Survival  (weeks) 13 26 0.014
[object Object],[object Object],Progression free-survival FFCD 0301:  strategic trial: which 1rst line and 2d line ? ARM A FUP -> Gem ARM B Gem -> FUP P (log-rank) Median mths   [95% CI] 6.63  [5.27 – 8.07] 8.03  [5.93 – 9.97] 0.77 ARM A ARM B P Median  mths  [95% CI] 3.83 [2.36 – 7.03] 4.73  [2.43-8.23] 0.9
Recommendations for second line tt ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Medical treatment of metastatic pancreatic cancer ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
venous thromboembolic event : VTE Advanced pancreatic adenocarcinoma :  CONKO 004 trial  Efficacy of preventive anticoagulation ? LMWH decreases the risk of VTES But does not influence significantly the OS H. Riess  et al ., ASCO 2010, , A 4033 énoxaparine (Lovenox ® ) 1 mg/kg/j for 3 months then 40 mg/j N = 312 CT N = 152 CT +  enoxaparine N = 160 p   VTE  at  3 months 9,9 % 1,25 % < 0,01 VTE  at  12 months 15% 5% severes haemorragic Complications   ns TTP 5.4 months 5 months P  = 0.94 Overall Survival 8 months 8.3 months P  = 0.5
[object Object],[object Object],[object Object],[object Object],[object Object]
Gemcitabine:  mechanism of action Human equilibrative nucleoside transporter 1 (hENT1) Human concentrative nucleoside transporter 1 (hCNT1) Human concentrative nucleoside transporter 3 (hCNT3) CDA: gemcitabine catabolism enzyme
[object Object],[object Object],[object Object],[object Object],hENT1 low hENT1 elevated p OS PFS 13.3 months 8.4 months Not reached 46.8 months 0.0001 hCNT3 low hCNT3 elevated OS PFS 12.6 months 8.6 months Not reached 23.5 months 0.02
CDA: enzyme of gemcitabine   catabolism cytidine deaminase (CDA) enzymatic activity and toxicity/efficacy of gemcitabine (?) ACTIVE  METABOLITES 2’-dFdU (inactive) Cytidine Deaminase (CDA) gene polymorphism Gemzar ®
Adjuvant treatment of pancreatic cancer ,[object Object],[object Object],[object Object]
In absence of metastase and local infiltration: Whipple = Cephalic Duodeno Pancreatectomy
non-resecability criteria  ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Stenting in case of icterus in non resectable case or metastses
Quality of Pathological exam +++
Medical treatment of metastatic pancreatic cancer ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
9 m vs 11 m p = 0,01 11 m vs 20 m p = 0,03
[object Object],[object Object],[object Object],[object Object],ESPAC 1: Radiochimiotherapy  vs   no radiochimiotherapy : 5 year’survival  10% vs 20% (p = 0.05 ) Neoptolemos JP, NEJM, 2004
ESPAC1: Chemotherapy  vs   No chemotherapy : Survival at 5 years  21% vs 8% (p = 0.009)
DFS : 13.4  vs   6.9 m p < 0.001 Overall survival : 22.1  vs   20.2 m p < 0.06   CONKO-001:adjuvant Gemcitabine ?
Neoptolemos J, ASCO 2009, LBA4505 = No  difference ESPAC 3 (V2): FU/FA or Gem ? Survival ESPAC 3 (V2): Toxicity Grade 3-4 5-FU/AF Gemcitabine p Thrombopénie 0 % 1,5 % 0,0034 Mucite  10 % 0 % < 0,001 Diarrhée 13 % 2 % < 0,001
SYNTHESIS:  MEDICAL TREATMENTS IN PANCREATIC CANCER IN 2011: METASTASES (1) ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],SYNTHESIS:  MEDICAL TREATMENTS IN PANCREATIC CANCER IN 2011: METASTASES (2)
[object Object],[object Object],[object Object],[object Object],SYNTHESIS:  MEDICAL TREATMENTS IN PANCREATIC CANCER IN 2011:  ADJUVANT

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MON 2011 - Slide 21 - P. Rougier - Gastric and pancreatic cancers (part II)

  • 1. Medical treatment of pancreatic cancer UVSQ University of Versailles Saint Quentin en yveline Philippe Rougier Digestive Oncology Hopital Européen Georges Pompidou 75015 Paris ; France [email_address] Pancreas: A complex anatomy
  • 2.
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  • 4. 1997: Gemcitabine became a standard of care in advanced pancreatic cancer 0 2 4 6 8 10 12 14 16 18 20 100 80 60 40 20 0 Weekly b 5-FU Weekly Gemcitabine Survival time (months) Patients surviving (%) 1 Burris H, et al. J Clin Oncol 1997;15:2403 – 13 Gemcitabine 5-FU p Median survival (mo) 5.65 4.41 0.0025 Clinical benefit (%) 23.8 4.8 0.0022 1-year survival (%) 18 2
  • 5. Heinemann V, BMC Cancer 2008 Platin salts Fluoropyrimidines Autres in favor of Gem + X in favor of Gem alone Meta-analysis: combinations in first line Not done on individal data G + Platinum salts G + FU derivatives
  • 6.
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  • 8. Disease characteristics T. Conroy et al ., ASCO 2010, A 4010 ; N Engl J Med 2011 in press Characteristic Folfirinox N=171 Gemcitabine N=171 p Synchronous metastases Metachronous metastases 156 (91.2%) 15 (8.8%) 161 (94.2%) 10 (5.8%) NS NS Median nr. of T sites CA19-9  59 ULN 2 (1-6) 68 (41.5%) 2 (1-6) 77 (46.7%) NS NS Measurable site Liver Pancreas Nodes Lungs Peritoneal 149 (88.2%) 89 (52.7%) 48 (28.4%) 33 (19.5%) 33 (19.5%) 150 (87.7%) 91 (53.2%) 39 (22.8%) 49 (28.7%) 32 (18.7%) NS NS NS 0.049 NS
  • 9. Safety: hematological adverse events (Aes) 5.4 42.5% of the pts received G-CSF in the F arm vs 5.3% in the G arm One toxic death occurred in each arm T. Conroy et al ., ASCO 2010, A 4010 ; N Engl J Med 2011 in press AE, % per patient Folfirinox N=167 Gemcitabine N=169 p All Grade 3/4 All Grade 3/4 Grade 3/4 Neutropenia 79.9 45.7 54.8 18.7 0.0001 Febrile Neutropenia 7.2 2.4 0.6 0.009 Anemia 90.4 7.8 94.6 5.4 NS Thrombocytopen. 75.2 9.1 54.8 2.4 0.008
  • 10. Objective Response Rate T. Conroy et al ., ASCO 2010, A 4010 ; N Engl J Med 2011 in press Folfirinox N=171 Gemcitabine N=171 p Complete response 0.6% 0% Partial response 31% 9.4% 0.0001 CR/PR 95% CI [24.7-39.1] [5.9-15.4] Stable disease 38.6% 41.5% Disease control CR+PR+SD 70.2% 50.9% 0.0003 Progression 15.2% 34.5% Not assessed 14.6% 14.6% Median duration of response 5.9 mo. 4 mo. ns
  • 11. Progression-Free Survival Median PFS Folfirinox: 6.4 mo. Median PFS Gemcitabine: 3.3 mo HR (95% CI): 0.47 (0.37-0.59) ; p < 0.0001 T. Conroy et al ., ASCO 2010, A 4010 ; N Engl J Med 2011 in press
  • 12. Overall Survival T. Conroy et al ., ASCO 2010, A 4010 ; N Engl J Med 2011 in press Median survival [CI 95%]: 11.1 mo .[ 9 - 13.1] vs 6.8 mo .[ 5.5 - 7.6] P = <0.0001 ; HR = 0.57 [0.45 – 0.73]
  • 13. Time to definitive QoL degradation T. Conroy et al ., ASCO 2010, A 4010 ; N Engl J Med 2011 in press
  • 14.
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  • 18. Conatumumab / AMG 479, phase II in Metastatic Pancreatic Cancer … phase III in progress Patients à risque H. L. Kindler et al ., ASCO 2010, A 4035 Trend in favor of anti IGFR efficacy ? Events Median OS (95% CI), mthis HR (95% CI) a p Conatumumab + gemcitabine 32 (78%) 7.5 (4.8, 10.0) 0.87 (0.53, 1.43) 0.59 AMG 479 + gemcitabine 29 (69%) 8.7 (5.3, 12.2) 0.67 (0.41, 1.12) 0.12 Placebo + gemcitabine 34 (81%) 5.9 (4.1, 9.7) 41 39 38 33 29 25 23 23 19 14 14 11 7 5 3 1 0 0 0 0 0 0 0 0 0 42 39 37 34 30 28 22 21 20 17 17 15 13 8 6 6 4 3 3 3 2 1 1 1 0 42 39 38 30 26 20 19 16 15 14 13 12 6 3 2 2 1 1 1 1 0 0 0 0 0 0.0 0.2 0.4 0.6 0.8 1.0 Survie globale 0 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 Mois
  • 19.
  • 20. Clinical trials investigating second-line chemotherapy in gemcitabine-pretreated pts with advanced pancreatic cancer c c Treatment regimen No. of patients KPS 90-100% / ECOG 0-1 Metastatic disease (%) RR (%) DCR (%) PFS/TTP (months) OS (months) Oxa/5-FU CI/LV vs BSC 46 NA NA NA NA OFF:5.25 BSC:2.5 OFF:10 BSC:8.5 Oxa/5-FU CI/LV vs 5-FU CI/LV (nb = 168) OFF:77 FF: 91 OFF:54% FF: 50 % OFF:85.5 FF: 89.2 NA NA OFF:3.25 FF: 2.25 OFF:6.5 FF: 3.25 Oxa/5-FU CI/LV 30 33 % 97 23 53 5.1 5.8 FOLFOX-4 42 62 % 83 14 52 4 6.7 Modified FOLFOX 30 97 % NA NA 20 1.4 4 vs modified FOLFIRI 30 100 % 28 1.9 4 Oxa + Gem 33 88 % 64 21 58 4.2 6.0 Oxa + Cap 39 80 % NA 3 23 NA 5.8 Oxa + irinotecan 30 30 % 100 10 33 4.1 5.9 Oxa + raltitrexed 41 61 % 100 24 51 1.8 5.2 Cisplatin + irinotecan + Gem + 5-FU + LV 34 NA 100 24 44 3.9 10.3 Cap + Gem + docetaxel 35 52 100 29 60 NA 11.2
  • 21. 5FU- Folinic-Ac (FF) Oxaliplatin-5FU- Folinic-Ac (OFF) non resecable Cancer (Localy avanced or Metastatic) Progression under Gem Karnowsky >60 n=165 Pelzer et al, ASCO 2008 A 4508 FF : 5FU 2000 mg/m²/24h, ac. folinic 200 mg/m² in 30 mn D1- D 8- D 15- D 22 OFF : FF + Oxaliplatin 85 mg/m² D 8- D 22 D 1= D 43 Primary endpoint : Overall Survival Second line chemotherapy: CONKO-3 trial R Per protocol FF OFF p PFS (weeks) 9 13 0.012 Overall Survival (weeks) 13 26 0.014
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  • 25. venous thromboembolic event : VTE Advanced pancreatic adenocarcinoma : CONKO 004 trial Efficacy of preventive anticoagulation ? LMWH decreases the risk of VTES But does not influence significantly the OS H. Riess et al ., ASCO 2010, , A 4033 énoxaparine (Lovenox ® ) 1 mg/kg/j for 3 months then 40 mg/j N = 312 CT N = 152 CT + enoxaparine N = 160 p VTE at 3 months 9,9 % 1,25 % < 0,01 VTE at 12 months 15% 5% severes haemorragic Complications   ns TTP 5.4 months 5 months P = 0.94 Overall Survival 8 months 8.3 months P = 0.5
  • 26.
  • 27. Gemcitabine: mechanism of action Human equilibrative nucleoside transporter 1 (hENT1) Human concentrative nucleoside transporter 1 (hCNT1) Human concentrative nucleoside transporter 3 (hCNT3) CDA: gemcitabine catabolism enzyme
  • 28.
  • 29. CDA: enzyme of gemcitabine catabolism cytidine deaminase (CDA) enzymatic activity and toxicity/efficacy of gemcitabine (?) ACTIVE METABOLITES 2’-dFdU (inactive) Cytidine Deaminase (CDA) gene polymorphism Gemzar ®
  • 30.
  • 31. In absence of metastase and local infiltration: Whipple = Cephalic Duodeno Pancreatectomy
  • 32.
  • 33. Stenting in case of icterus in non resectable case or metastses
  • 35.
  • 36. 9 m vs 11 m p = 0,01 11 m vs 20 m p = 0,03
  • 37.
  • 38. ESPAC1: Chemotherapy vs No chemotherapy : Survival at 5 years 21% vs 8% (p = 0.009)
  • 39. DFS : 13.4 vs 6.9 m p < 0.001 Overall survival : 22.1 vs 20.2 m p < 0.06 CONKO-001:adjuvant Gemcitabine ?
  • 40. Neoptolemos J, ASCO 2009, LBA4505 = No difference ESPAC 3 (V2): FU/FA or Gem ? Survival ESPAC 3 (V2): Toxicity Grade 3-4 5-FU/AF Gemcitabine p Thrombopénie 0 % 1,5 % 0,0034 Mucite 10 % 0 % < 0,001 Diarrhée 13 % 2 % < 0,001
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  • 43.