drugset / Trial / NCT03875781

Non Inferiority Study of Preoperative Chemotherapy Without Pelvic Irradiation for Rectal Cancer

NCT03875781 ↗

Phase 3 Recruiting 540 enrolled Assistance Publique - Hôpitaux de Paris
RandomizedParallel-groupOpen-labelTreatment

Summary

This study is a non-inferiority phase III randomised trial comparing preoperative chemotherapy alone (modified FOLFIRINOX) to chemotherapy followed by chemoradiotherapy in patients with primary resectable locally advanced rectal cancer. The primary endpoint of the study is 3-year progression free survival. Expected 3 year PFS rate in the preoperative chemotherapy followed by chemoradiotherapy arm is 75%. This hazard rate, in an exponential survival model, corresponds to a decrease in the 3-year PFS rate on the preoperative chemotherapy arm to 67%. The study will randomize 540 patients (270 in the chemotherapy group and 270 in the chemoradiotherapy group) in 42 french academic centers.

Timeline

Start
2019-06-05
Primary completion
2026-12-05
Completion
2026-12-05

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Capecitabine Small molecule 825 mg/m2 —
Background Irinotecan Small molecule 180 mg/m2 —
Background Leucovorin Small molecule 400 mg/m2 —
Background Oxaliplatin Small molecule 85 mg/m2 —
Background fluorouracil Small molecule — —

Indications