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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 Individual Participant Data Network Meta-Analysis of Neoadjuvant Chemotherapy or Chemoradiotherapy in Esophageal or Gastroesophageal Junction Carcinoma
Creator Faron et al.
Author Matthieu Faron
Author Maurice Cheugoua-Zanetsie
Author Jayne Tierney
Author Pierre Thirion
Author Matthew Nankivell
Author Kathryn Winter
Author Hong Yang
Author Joel Shapiro
Author Dewi Vernerey
Author B. Mark Smithers
Author Thomas Walsh
Author Guillaume Piessen
Author Magnus Nilsson
Author Jurjen Boonstra
Author Marc Ychou
Author Simon Law
Author David Cunningham
Author Florent de Vathaire
Author Michael Stahl
Author Susan Urba
Author Michele Valmasoni
Author Danièle Williaume
Author Janine Thomas
Author Florian Lordick
Author Joel Tepper
Author Jack Roth
Author Val Gebski
Author Bryan Burmeister
Author Xavier Paoletti
Author Johanna van Sandick
Author Jianhua Fu
Author Jean-Pierre Pignon
Author Michel Ducreux
Author Stefan Michiels
Abstract PURPOSE: The optimal neoadjuvant treatment for resectable carcinoma of the thoracic esophagus (TE) or gastroesophageal junction (GEJ) remains a matter of debate. We performed an individual participant data (IPD) network meta-analysis (NMA) of randomized controlled trials (RCTs) to study the effect of chemotherapy or chemoradiotherapy, with a focus on tumor location and histology subgroups. PATIENTS AND METHODS: All, published or unpublished, RCTs closed to accrual before December 31, 2015 and having compared at least two of the following strategies were eligible: upfront surgery (S), chemotherapy followed by surgery (CS), and chemoradiotherapy followed by surgery (CRS). All analyses were conducted on IPD obtained from investigators. The primary end point was overall survival (OS). The IPD-NMA was analyzed by a one-step mixed-effect Cox model adjusted for age, sex, tumor location, and histology. The NMA was registered in PROSPERO (CRD42018107158). RESULTS: IPD were obtained for 26 of 35 RCTs (4,985 of 5,807 patients) corresponding to 12 comparisons for CS-S, 12 for CRS-S, and four for CRS-CS. CS and CRS led to increased OS when compared with S with hazard ratio (HR) = 0.86 (0.75 to 0.99), P = .03 and HR = 0.77 (0.68 to 0.87), P < .001 respectively. The NMA comparison of CRS versus CS for OS gave a HR of 0.90 (0.74 to 1.09), P = .27 (consistency P = .26, heterogeneity P = .0038). For CS versus S, a larger effect on OS was observed for GEJ versus TE tumors (P = .036). For the CRS versus S and CRS versus CS, a larger effect on OS was observed for women (P = .003, .012, respectively). CONCLUSION: Neoadjuvant chemotherapy and chemoradiotherapy were consistently better than S alone across histology, but with some variation in the magnitude of treatment effect by sex for CRS and tumor location for CS. A strong OS difference between CS and CRS was not identified.
Publication Journal of Clinical Oncology: Official Journal of the American Society of Clinical Oncology
Volume 41
Issue 28
Pages 4535-4547
Date 2023-10-01
Journal Abbr J Clin Oncol
Language eng
DOI 10.1200/JCO.22.02279
ISSN 1527-7755
Library Catalog PubMed
Extra PMID: 37467395 PMCID: PMC10553121
Tags Carcinoma, Chemoradiotherapy, Chemotherapy, Adjuvant, Esophageal Neoplasms, Esophagogastric Junction, Female, Humans, Male, Neoadjuvant Therapy, Network Meta-Analysis, Randomized Controlled Trials as Topic
Date Added 2023/11/15 - 14:56:30
Date Modified 2024/10/10 - 16:26:22
Notes and Attachments PubMed entry (Attachment)
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