drugset / Trial / NCT04518280

Short-course Radiotherapy Based TNT Combined With PD-1 Inhibitor for Locally Advanced Rectal Cancer

NCT04518280 ↗

Phase 2 Completed 130 enrolled Fudan University
RandomizedParallel-groupOpen-labelTreatment

Summary

TORCH is a prospective, multicentre, randomized phase II trial. 130 LARC (T3-4/N+M0, distance from anal verge ≤12cm) patients will be treated with total neoadjuvant therapy (TNT) and assigned to Group A and Group B. Group A receives SCRT (25Gy/5Fx) followed by 6 cycles of Toripalimab combined with CAPOX (ToriCAPOX). Group B receives 2 cycles of ToriCAPOX followed by SCRT and 4 cycles of ToriCAPOX. TME surgery is scheduled after TNT while a watch and wait (W\&W) option can be applied to patients achieving clinical complete response (cCR). The primary endpoint is complete response (CR, pathological complete response \[pCR\] plus cCR) rate. The secondary endpoints include the grade 3-4 acute adverse effects (AE) rate, 3-year DFS rate, etc.

Timeline

Start
2021-05-01
Primary completion
2023-09-01
Completion
2025-01-01

Outcome

Met primary endpoint

paper Both groups fulfilled the predefined statistical hypothesis (P < .001). PMID 38950321 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Capecitabine Small molecule 1000 mg/m2 —
Subject Oxaliplatin Small molecule 130 mg/m2 —
Subject Toripalimab Monoclonal antibody 240 mg —

Indications

No indication recorded.