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Study identifier: NCT07467434 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

FOLFIRINOX Induction Chemotherapy for Synchronous Liver Metastases

Condition: Rectal Cancer · Synchronous Liver Metastases · Antineoplastic Combined Chemotherapy Protocols  ·  Sponsor: Assistance Publique - Hôpitaux de Paris

PhaseN/A
Planned participants550
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Stéphane BENOIST, MD PhD  ·  +33 (0)1 45 21 34 72  ·  stephane.benoist@aphp.fr

Solafah ABDALLA, MD PhD  ·  +33 (0)1 45 21 34 70  ·  solafah.abdalla@aphp.fr

Always discuss trial participation with your own doctor first.

Locations (1)

Digestive Surgery Department, Bicêtre University Hospital AP-HPLe Kremlin-Bicêtre, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT07467434