Modified FOLFIRINOX Versus CISGEM Chemotherapy for Patients With Advanced Biliary Tract Cancer (PRODIGE 38 AMEBICA): A Randomized Phase II Study

Author:

Phelip Jean marc1ORCID,Desrame Jérôme2,Edeline Julien3ORCID,Barbier Emilie4,Terrebonne Eric5,Michel Pierre6,Perrier Hervé7,Dahan Laetitia8ORCID,Bourgeois Vincent9,Akouz Faiza Khemissa10,Soularue Emilie11,Ly Valérie Lebrun12,Molin Yann13,Lecomte Thierry14,Ghiringhelli François15,Coriat Romain16ORCID,Louafi Samy17,Neuzillet Cindy18,Manfredi Sylvain19ORCID,Malka David20ORCID,

Affiliation:

1. INSERM U1059, Université Jean Monnet, CHU de Saint Etienne, Hôpital Nord, Saint-Etienne, France

2. Hôpital privé Jean Mermoz, Lyon, France

3. Centre Eugène Marquis, Rennes, France

4. FFCD, EPICAD INSERM LNC-UMR 1231, Dijon, France

5. Hôpital Haut-Lévêque, Pessac, France

6. CHU Charles Nicolle, Rouen, France

7. Hôpital Saint Joseph, Marseille, France

8. CHU la Timone, Marseille, France

9. Hôpital Duchenne, Boulogne sur mer, France

10. CH Perpignan, Perpignan, France

11. Hôpital de Bicêtre, le Kremlin Bicêtre, France

12. CHU Dupuytren, Limoges, France

13. Clinique de La Sauvegarde, Lyon, France

14. Hôpital Trousseau, Tours, France

15. Centre Georges-François Leclerc, Dijon, France

16. CHU Cochin, Paris, France

17. Centre Hospitalier Sud Francilien, Corbeil-Essonnes, France

18. Curie Institute, Saint Cloud, France

19. INSERM U1231, Université Bourgogne, Franche Comté, CHU Le Bocage, Dijon, France

20. Gustave Roussy, Université Paris Saclay, Villejuif, France

Abstract

PURPOSE Whether triplet chemotherapy is superior to doublet chemotherapy in advanced biliary tract cancer (BTC) is unknown. METHODS In this open-label, randomized phase II-III study, patients with locally advanced or metastatic BTC and an Eastern Cooperative Oncology Group performance status of 0 or 1 were randomly assigned (1:1) to receive oxaliplatin, irinotecan, and infusional fluorouracil (mFOLFIRINOX), or cisplatin and gemcitabine (CISGEM) for a maximum of 6 months. We report the results of the phase II part, where the primary end point was the 6-month progression-free survival (PFS) rate among the patients who received at least one dose of treatment (modified intention-to-treat population) according to Response Evaluation Criteria in Solid Tumors version 1.1 (statistical assumptions: 6-month PFS rate ≥ 59%, 73% expected). RESULTS A total of 191 patients (modified intention-to-treat population, 185: mFOLFIRINOX, 92; CISGEM, 93) were randomly assigned in 43 French centers. After a median follow-up of 21 months, the 6-month PFS rate was 44.6% (90% CI, 35.7 to 53.7) in the mFOLFIRINOX arm and 47.3% (90% CI, 38.4 to 56.3) in the CISGEM arm. Median PFS was 6.2 months (95% CI, 5.5 to 7.8) in the mFOLFIRINOX arm and 7.4 months (95% CI, 5.6 to 8.7) in the CISGEM arm. Median overall survival was 11.7 months (95% CI, 9.5 to 14.2) in the mFOLFIRINOX arm and 13.8 months (95% CI, 10.9 to 16.1) in the CISGEM arm. Adverse events ≥ grade 3 occurred in 72.8% of patients in the mFOLFIRINOX arm and 72.0% of patients in the CISGEM arm (toxic deaths: mFOLFIRINOX arm, two; CISGEM arm, one). CONCLUSION mFOLFIRINOX triplet chemotherapy did not meet the primary study end point. CISGEM doublet chemotherapy remains the first-line standard in advanced BTC.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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