Karine Le Malicot

ORCID: 0000-0002-3226-8525
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About
Contact & Profiles
Research Areas
  • Colorectal Cancer Treatments and Studies
  • Gastric Cancer Management and Outcomes
  • Genetic factors in colorectal cancer
  • Colorectal Cancer Surgical Treatments
  • Pancreatic and Hepatic Oncology Research
  • Colorectal and Anal Carcinomas
  • Cancer Treatment and Pharmacology
  • Hepatocellular Carcinoma Treatment and Prognosis
  • Cancer Genomics and Diagnostics
  • Neuroendocrine Tumor Research Advances
  • Colorectal Cancer Screening and Detection
  • Radiomics and Machine Learning in Medical Imaging
  • Gastrointestinal Tumor Research and Treatment
  • Lung Cancer Research Studies
  • Cancer Immunotherapy and Biomarkers
  • Neuroblastoma Research and Treatments
  • Cholangiocarcinoma and Gallbladder Cancer Studies
  • Metastasis and carcinoma case studies
  • Health Systems, Economic Evaluations, Quality of Life
  • Statistical Methods in Clinical Trials
  • Renal cell carcinoma treatment
  • Economic and Financial Impacts of Cancer
  • Cervical Cancer and HPV Research
  • Lung Cancer Treatments and Mutations
  • Esophageal Cancer Research and Treatment

Fédération Francophone de Cancérologie Digestive
2016-2025

Université de Bourgogne
2015-2025

Inserm
2016-2025

Centre de recherche Translationnelle en Médecine moléculaire
2019-2024

Université Bourgogne Franche-Comté
2019

Université Paris Cité
2016-2018

Hôpital Européen Georges-Pompidou
2016-2018

Centre Georges François Leclerc
2018

CHU Dijon Bourgogne
2017

Centre Jean Perrin
2016

The prognostic value of BRAF and KRAS mutations within microsatellite-unstable (MSI) microsatellite-stable (MSS) subgroups resected colon carcinoma patients remains controversial. We examined this question in prospectively collected biospecimens from stage III cancer with separate analysis MSI MSS tumors receiving adjuvant FOLFOX +/- cetuximab two therapy trials.

10.1093/jnci/djw272 article EN JNCI Journal of the National Cancer Institute 2016-10-21
Astrid Lièvre Anthony Turpin Isabelle Ray‐Coquard Karine Le Malicot Juliette Thariat and 95 more Guido Ahle Cindy Neuzillet Xavier Paolettí Olivier Bouché Kaïs Aldabbagh Pierre Michel D. Debieuvre A. Cañellas Marie Wislez Lucie Laurent May Mabro Raphaël Colle Anne‐Claire Hardy‐Bessard Laura Mansi Émeline Colomba Jean Bourhis Philippe Gorphe Y. Pointreau Ahmed Idbaïh Rénata Ursu Anna Luisa Di Stefano Gérard Zalcman Thomas Aparicio Solenne Moulin O. Leleu S Leparrée H. Goasdoué Christine Piprot G. Tourneur Vincent Bayart Delphine Lignier Emma Lachaier Marwa Khamari Alexandre Coutté N. Siembida Aline Houessinon Jean Marc Regimbeau Bruno Chauffert Aurélie Moreira Vincent Hautefeuille C.S.L. Sew Hee Mathieu Boone Céline Bihan E. Chive Stéphane Poulet-Potriquier Rachida Fahem Dominique Luet Guillaume Roquin Carole Vitellius Nathanaëlle Cornet-Trichereau François‐Xavier Caroli‐Bosc Anne Thirot‐Bidault Stanislas Ropert Julie Gachet - Masson Mélanie Dehais Gwen-Ael L'helgoualc'h Ibrahim Ali-Mahamadou Safia Talfi L. Belmont Dieudonné Kilendo Nasro Benrezzak Emeline Dubief Guillaume Conroy Laurence Delique Maud Basso Isabelle Pons Karine Salignon Anne-Laure Villing Emmanuelle Mougenot Cassandra Porebski Asma Guiatni Nicolas Cloarec Laurent Mineur Marie Bouchaud C David Annie Peytier Thomas Greletty Franck Audemar Emanuelle Vignes Floriane Minne Guillaume Goldzak Fabienne Huysman Fayçal Hocine Zaher Lakkis Laura Mansi Guillaume Meynard Hamadi Almotlak Élodie Klajer Xu-Shan Sun Laura Mansi Julie Wasselin Pascale Catala Claire Mazuy H. Vandamme Jean-Briac Prevost

10.1016/j.ejca.2020.09.035 article EN publisher-specific-oa European Journal of Cancer 2020-10-08

The prognostic value of BRAF and KRAS mutations in patients who have undergone resection for colon cancer been treated with combination leucovorin, fluorouracil, oxaliplatin (FOLFOX)-based adjuvant chemotherapy is controversial, possibly owing to a lack stratification on mismatch repair status.To examine the effect stage III FOLFOX or without cetuximab.This study included available tumor blocks resected adenocarcinoma participated between December 2005 November 2009 PETACC-8 phase randomized...

10.1001/jamaoncol.2015.5225 article EN JAMA Oncology 2016-01-15

The objective of this study was to build and validate a radiomic signature predict early poor outcome using baseline 2-month evaluation CT compare it the RECIST1·1 morphological criteria defined by changes in homogeneity borders.This is an ancillary from PRODIGE-9 multicentre prospective for which 491 patients with metastatic colorectal cancer (mCRC) treated 5-fluorouracil, leucovorin irinotecan (FOLFIRI) bevacizumab had been analysed. In 230 patients, computed texture analysis performed on...

10.1136/gutjnl-2018-316407 article EN Gut 2019-05-17

Objective Diagnostic tests, such as Immunoscore, predict prognosis in patients with colon cancer. However, additional prognostic markers could be detected on pathological slides using artificial intelligence tools. Design We have developed a software to detect tumour, healthy mucosa, stroma and immune cells CD3 CD8 stained slides. The lymphocyte density surface area were quantified automatically the tumour core (TC) invasive margin (IM). Using LASSO algorithm, DGMate (DiGital tuMor...

10.1136/gutjnl-2019-319292 article EN cc-by-nc Gut 2019-11-28

Purpose Conflicting results are reported for maintenance treatment with bevacizumab during chemotherapy-free intervals (CFI) in metastatic colorectal cancer after induction chemotherapy. Patients and Methods In this open-label, phase III, randomized controlled trial, we compared the tumor control duration (TCD) observed no (observation) CFI subsequent to chemotherapy 12 cycles of fluorouracil, leucovorin, irinotecan plus bevacizumab. After disease progression, regimen was repeated eight...

10.1200/jco.2017.75.2931 article EN Journal of Clinical Oncology 2018-01-18

We know of no data on the prognostic value primary tumor location (PTL) according to BRAF, RAS, and microsatellite instability (MSI) status in patients who have undergone resection for colon cancer (CC) been treated with current standard adjuvant chemotherapy.To determine predictive PTL MSI stage III CC receiving treatment FOLFOX (folinic acid [leucovorin calcium], fluorouracil, oxaliplatin) or without cetuximab.This post hoc analysis included available blocks resected adenocarcinoma...

10.1001/jamaoncol.2017.3695 article EN JAMA Oncology 2017-11-22

Previous pharmacogenetic studies have shown the prognostic impact of several rare dihydropyrimidine dehydrogenase gene (DPYD) variants on fluorouracil-related adverse events (fluorouracil AEs). However, conflicting results highlight need for prospective validation in large, homogeneous patient populations uniformly treated with current standard combination therapies used colon cancer (CC).To determine DPYD fluorouracil AEs patients stage III CC a fluorouracil, leucovorin, and oxaliplatin...

10.1001/jamaoncol.2015.5392 article EN JAMA Oncology 2016-01-21

Metastatic pancreatic cancer (mPC) still harbors a dismal prognosis. Our previous trial (PRODIGE 4-ACCORD 11) demonstrated the superiority of 6-month chemotherapy with fluorouracil, leucovorin, irinotecan, and oxaliplatin (FOLFIRINOX) over gemcitabine for overall survival. The high limiting oxaliplatin-related neurotoxicity supports evaluation an stop-and-go strategy sequential in mPC.In this phase II study, patients were randomly assigned to receive either 6 months FOLFIRINOX (arm A), 4...

10.1200/jco.20.03329 article EN Journal of Clinical Oncology 2021-07-21

Abstract Purpose: The consensus molecular subtypes (CMS) represent a significant advance in the understanding of intertumor heterogeneity colon cancer. Intratumor (ITH) is new frontier for refining prognostication and treatment resistance. This study aims at deciphering transcriptomic ITH cancer its potential prognostic implications. Experimental Design: We deconvoluted profiles 1,779 tumors from PETACC8 trial 155 cell lines as weighted sums four CMSs, using Weighted In Silico Pathology...

10.1158/1078-0432.ccr-21-0529 article EN cc-by-nc-nd Clinical Cancer Research 2021-06-24

Only 1 randomized clinical trial has shown the superiority of immune checkpoint inhibitors in patients with deficient mismatch repair and/or microsatellite instability (dMMR/MSI) metastatic colorectal cancer (mCRC) first-line setting.To determine whether avelumab (an anti-programmed cell death ligand antibody) improves progression-free survival (PFS) compared standard second-line chemotherapy dMMR/MSI mCRC.The SAMCO-PRODIGE 54 is a national open-label phase 2 that was conducted from April...

10.1001/jamaoncol.2023.2761 article EN cc-by-nc-nd JAMA Oncology 2023-08-03

A dramatic increase in the incidence of diffuse form gastric adenocarcinomas and particularly signet ring cell carcinomas has been observed Western countries. Evidence is accruing that may have inherent chemo resistance leaving many clinicians unsure benefits delaying surgery to pursue a neoadjuvant approach. PRODIGE-19-FFCD1103-ADCI002 prospective multicentre controlled randomised phase II/III trial comparing current standard care perioperative chemotherapy (2x3 cycles Epirubicin,...

10.1186/1471-2407-13-281 article EN cc-by BMC Cancer 2013-06-10

4000 Background: Metastatic pancreatic cancer (mPC) still harbors a dismal prognosis (5-year overall survival [OS] <5%). Our previous trial (PRODIGE4-ACCORD11) has demonstrated the superiority of 6-month [m] chemotherapy with FOLFIRINOX over gemcitabine in terms progression-free [PFS] (6.4 vs. 3.3 m; HR: 0.47; 95%CI: 0.37-0.59; p<0.001) and OS (11.1 6.8 0.57; 0.45-0.73; p<0.001), at expense higher toxicity, notably cumulative, often limiting, peripheral neuropathy oxaliplatin. In this...

10.1200/jco.2018.36.15_suppl.4000 article EN Journal of Clinical Oncology 2018-05-20
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