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Epitranscriptomics & Cancer Adaptation : A.David

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Our research work focuses on the contribution of post-transcriptional mechanisms on cancer cell adaptation, in particular RNA epigenetic & translational control.

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Group name EquipeMY
Item Type Journal Article
Title Chemotherapy (doublet or triplet) plus targeted therapy by RAS status as conversion therapy in colorectal cancer patients with initially unresectable liver-only metastases. The UNICANCER PRODIGE-14 randomised clinical trial
Creator Ychou et al.
Author Marc Ychou
Author Michel Rivoire
Author Simon Thezenas
Author Rosine Guimbaud
Author Anne Mercier-Blas
Author Laurent Mineur
Author Eric Francois
Author Faiza Khemissa
Author Marion Chauvenet
Author Reza Kianmanesh
Author Marianne Fonck
Author Philippe Houyau
Author Thomas Aparicio
Author Marie-Pierre Galais
Author Franck Audemar
Author Eric Assenat
Author Evelyne Lopez-Crapez
Author Claire Jouffroy
Author Antoine Adenis
Author René Adam
Author Olivier Bouché
Abstract BACKGROUND: Colorectal cancer (CRC) patients have a better prognosis if metastases are resectable. Initially, unresectable liver-only metastases can be converted to resectable with chemotherapy plus a targeted therapy. We assessed which of chemotherapy doublet (2-CTx) or triplet (3-CTx), combined with targeted therapy by RAS status, would be better in this setting. METHODS: PRODIGE 14 was an open-label, multicenter, randomised Phase 2 trial. CRC patients with initially defined unresectable liver-only metastases received either, 2-CTx (FOLFOX or FOLFIRI) or 3-CTx (FOLFIRINOX), plus bevacizumab/cetuximab by RAS status. The primary endpoint was to increase the R0/R1 liver-resection rate from 50 to 70% with the 3-CTx. RESULTS: Patients (n?=?256) were mainly men with an ECOG PS of 0, and a median age of 60 years. In total, 109 patients (42.6%) had RAS-mutated tumours. After a median follow-up of 45.6 months, the R0/R1 liver-resection rate was 56.9% (95% CI: 48-66) with the 3-CTx versus 48.4% (95% CI: 39-57) with the 2-CTx (P?=?0.17). Median overall survival was 43.4 months with 3-CTx versus 40 months with 2-CTx. CONCLUSION: We failed to increase from 50 to 70% the R0/R1 liver-resection rate with the use of 3-CTx combined with bevacizumab or cetuximab by RAS status in CRC patients with initially unresectable liver metastases.
Publication British Journal of Cancer
Volume 126
Issue 9
Pages 1264-1270
Date 2022-05
Journal Abbr Br J Cancer
Language eng
DOI 10.1038/s41416-021-01644-y
ISSN 1532-1827
Library Catalog PubMed
Extra PMID: 34992255 PMCID: PMC9042909
Tags Antineoplastic Combined Chemotherapy Protocols, Bevacizumab, Camptothecin, Cetuximab, Colorectal Neoplasms, Fluorouracil, Humans, Leucovorin, Liver Neoplasms, Male, Middle Aged, Pancreatic Neoplasms
Date Added 2022/08/30 - 16:10:29
Date Modified 2024/10/10 - 16:31:38
Notes and Attachments PubMed entry (Attachment)


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