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NCT07467434Recruiting

FOLFIRINOX Induction Chemotherapy for Synchronous Liver Metastases

Multicenter Cohort Study of Mid/Lower Rectal Cancer With Resectable Synchronous Liver Metastases Treated With FOLFIRINOX Induction Chemotherapy

Source: ClinicalTrials.gov · Last updated 9 Jun 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Observational
Enrollment
550 (estimated)
First submitted
8 Mar 2026
Start date
1 May 2026
Primary completion date
1 Nov 2030
Lead sponsor
Assistance Publique - Hôpitaux de Paris
NCT number
NCT07467434

What you commit to

  • Study type: Observational
  • Planned participants: 550
  • From 1 May 2026 to the primary completion date, 1 Nov 2030
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Induction chemotherapy with FOLFIRINOX of less than 2 courses

Age

  • Minor under the age of 18.

Other

  • Presence of extrahepatic metastases

Who the study is looking for

  • Adult subjects aged 18 years and older
  • Adenocarcinoma of the middle and/or lower rectum pMMR T3, T4, and/or N+
  • Resectable synchronous liver metastases

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Digestive Surgery Department, Bicêtre University Hospital AP-HP
Coordinator of this site? Confirm its status
Le Kremlin-BicêtreFranceRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.