Clinical Trial

FOLFIRINOX Induction Chemotherapy for Synchronous Liver Metastases

Study acronym: SYNCHRONOX
Recruiting
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Summary
SYNCHRONOX is a multicenter cohort (retrospective then prospective) intending to include 550 patients with mid or low rectal adenocarcinoma (pMMR, T3-T4 and/or N+) and resectable synchronous liver metastases, treated upfront with at least two cycles of induction FOLFIRINOX chemotherapy. The primary objective is to determine, at 18 months, the R0 resection rate of both tumor sites (rectum and liver), while secondary objectives focus on 3 year overall and progression free survival, radiological and pathological responses, postoperative morbidity and mortality, and comparison of the different surgical strategies after FOLFIRINOX.
Protocol Amendment History 3 changes
critical Recruitment opened 2026-06-10
notable Primary completion pushed: 2030-10 -> 2030-11-01 2026-06-10
minor Completion pushed: 2034-04 -> 2034-05-01 2026-06-10
Trial Details
NCT Number NCT07467434
Lead Sponsor Assistance Publique - Hôpitaux de Paris
Conditions Rectal Cancer, Synchronous Liver Metastases, Antineoplastic Combined Chemotherapy Protocols, Surgical Therapy
Enrollment 550 participants
Start Date 2026-05-01
Primary Completion 2030-11-01 (estimated)
Study Completion 2034-05-01 (estimated)
Updated on ClinicalTrials.gov 2026-06-09