drugset / Trial / NCT01523457

Study of Modified FOLFIRINOX in Advanced Pancreatic Cancer

NCT01523457 ↗

Phase 2 Completed 75 enrolled Yale University
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The primary objective of this study was to determine the progression free survival in patients with metastatic pancreatic cancer and in patients with locally advanced unresectable non-metastatic pancreatic cancer treated with a dose-attenuated modification of folinic acid, fluorouracil, irinotecan, and oxaliplatin (FOLFIRINOX). Secondary endpoints included: determine objective response rate according to RECIST; determine overall survival; evaluate toxicity; determine rate of resection in locally advanced unresectable stratum; correlate time to progression, objective response, and overall survival with early changes in glucose metabolism using \[18F\]-fluorodeoxyglucose (FDG)-positron emission tomography (PET) scanning.

Timeline

Start
2011-10
Primary completion
2014-12
Completion
2015-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Irinotecan Small molecule 135 mg/m2 Intravenous
Subject Leucovorin Small molecule 400 mg/m2 Intravenous
Subject Oxaliplatin Small molecule 85 mg/m2 Intravenous
Subject fluorouracil Small molecule 300 mg/m2 Intravenous
Subject fluorouracil Small molecule 2400 mg/m2 Intravenous