drugset / Trial / NCT06652412

CGA Guided Ultrafractionated RT and Systemic Treatment in Elderly or Frail Patients with Inoperable Localized CRC

NCT06652412

Phase 2 Not yet recruiting 124 enrolled Fudan University
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This is a prospective, multicentre, cohort study. For cohort 1, experimental cohort, older or Frail patients with inoperable localized colorectal cancer will receive Ultrafractionated Radiotherapy (RT) and Comprehensive Geriatric Assessment (CGA) Guided systemic treatment. All patients will receive Ultrafractionated RT and PD-1 antibody. Furthermore, CGA will assess all patients and classify them into Frail, Vulnerabe, or Fit. Frail patients will receive Best Supportive Care (BSC); Vulnerabe patients will receive Fluorouracil/Raltitrexed and BSC; Fit patients will receive Fluorouracil/Raltitrexed, Oxaliplatin/Irinotecan, and BSC. For cohort 2, external control from real word, data of patients with the same baseline characteristics from the same period and the same institute will be prospectively collected. The primary endpoint is complete response (CR, pathological complete response \[pCR\] plus clinical complete response \[cCR\]) rate. The secondary endpoints include the grade 3-4 acute adverse effects rate, anal preservation rate, survival etc.

Timeline

Start
2024-11
Primary completion
2027-11
Completion
2028-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Capecitabine Small molecule
Subject Irinotecan Small molecule
Subject Oxaliplatin Small molecule
Subject Raltitrexed Small molecule
Subject Sintilimab Monoclonal antibody 200 mg
Subject fluorouracil Small molecule