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Molecular profiling of advanced soft-tissue sarcomas: the MULTISARC randomized trial.
Italiano, Antoine; Dinart, Derek; Soubeyran, Isabelle; Bellera, Carine; Espérou, Hélène; Delmas, Christelle; Mercier, Noémie; Albert, Sabrina; Poignie, Ludivine; Boland, Anne; Bourdon, Aurélien; Geneste, Damien; Cavaille, Quentin; Laizet, Yec'han; Khalifa, Emmanuel; Auzanneau, Céline; Squiban, Barbara; Truffaux, Nathalène; Olaso, Robert; Gerber, Zuzana; Wallet, Cédrick; Bénard, Antoine; Blay, Jean-Yves; Laurent-Puig, Pierre; Deleuze, Jean-François; Lucchesi, Carlo; Mathoulin-Pelissier, Simone.
Afiliação
  • Italiano A; Department of Medical Oncology, Institut Bergonié, University of Bordeaux, INSERM, Unité ACTION U1218, Bordeaux, France.
  • Dinart D; University of Bordeaux, Inserm, Bordeaux Population Health Research Center, UMR 1219, CIC-EC 1401/EUCLID Clinical Trials Platform, Bordeaux, France. d.dinart@bordeaux.unicancer.fr.
  • Soubeyran I; Unité de pathologie moléculaire, Institut Bergonié, Bordeaux, France. d.dinart@bordeaux.unicancer.fr.
  • Bellera C; Department of Biopathology, Institut Bergonié, U1218, Bordeaux, France.
  • Espérou H; University of Bordeaux, Inserm, Bordeaux Population Health Research Center, UMR 1219, CIC-EC 1401/EUCLID Clinical Trials Platform, Bordeaux, France.
  • Delmas C; Clinical Research and Clinical Epidemiology Unit, Institut Bergonié, Bordeaux, France.
  • Mercier N; Inserm, Pôle de Recherche Clinique, 75013, Paris, France.
  • Albert S; Inserm, Pôle de Recherche Clinique, 75013, Paris, France.
  • Poignie L; ANRS (France Recherche Nord&sud Sida-hiv Hépatites), Clinical Trial Safety and Public Health, Paris, France.
  • Boland A; University of Bordeaux, Inserm, Bordeaux Population Health Research Center, UMR 1219, CIC-EC 1401/EUCLID Clinical Trials Platform, Bordeaux, France.
  • Bourdon A; Clinical Research and Clinical Epidemiology Unit, Institut Bergonié, Bordeaux, France.
  • Geneste D; Clinical Research and Clinical Epidemiology Unit, Institut Bergonié, Bordeaux, France.
  • Cavaille Q; Université Paris-Saclay, CEA, Centre National de Recherche en Génomique Humaine, 91057, Evry, France.
  • Laizet Y; U1218, Institut Bergonié, Institut national de la santé et de la recherche médicale, Bordeaux, France.
  • Khalifa E; Bioinformatics unit, Institut Bergonié, Bordeaux, France.
  • Auzanneau C; U1218, Institut Bergonié, Institut national de la santé et de la recherche médicale, Bordeaux, France.
  • Squiban B; Bioinformatics unit, Institut Bergonié, Bordeaux, France.
  • Truffaux N; U1218, Institut Bergonié, Institut national de la santé et de la recherche médicale, Bordeaux, France.
  • Olaso R; Bioinformatics unit, Institut Bergonié, Bordeaux, France.
  • Gerber Z; U1218, Institut Bergonié, Institut national de la santé et de la recherche médicale, Bordeaux, France.
  • Wallet C; Bioinformatics unit, Institut Bergonié, Bordeaux, France.
  • Bénard A; Department of Biopathology, Institut Bergonié, U1218, Bordeaux, France.
  • Blay JY; Department of Biopathology, Institut Bergonié, U1218, Bordeaux, France.
  • Laurent-Puig P; Department of Biopathology, Institut Bergonié, U1218, Bordeaux, France.
  • Deleuze JF; Department of Biopathology, Institut Bergonié, U1218, Bordeaux, France.
  • Lucchesi C; Université Paris-Saclay, CEA, Centre National de Recherche en Génomique Humaine, 91057, Evry, France.
  • Mathoulin-Pelissier S; Université Paris-Saclay, CEA, Centre National de Recherche en Génomique Humaine, 91057, Evry, France.
BMC Cancer ; 21(1): 1180, 2021 Nov 05.
Article em En | MEDLINE | ID: mdl-34740331
BACKGROUND: Soft-tissue sarcomas (STS) represent a heterogeneous group of rare tumors including more than 70 different histological subtypes. High throughput molecular analysis (next generation sequencing exome [NGS]) is a unique opportunity to identify driver mutations that can change the usual one-size-fits-all treatment paradigm to a patient-driven therapeutic strategy. The primary objective of the MULTISARC trial is to assess whether NGS can be conducted for a large proportion of metastatic STS participants within a reasonable time, and, secondarily to determine whether a NGS-guided therapeutic strategy improves participant's outcome. METHODS: This is a randomized, multicentre, phase II/III trial inspired by the design of umbrella and biomarker-driven trials. The setting plans up to 17 investigational centres across France and the recruitment of 960 participants. Participants aged at least 18 years, with unresectable locally advanced and/or metastatic STS confirmed by the French sarcoma pathological reference network, are randomized according to 1:1 allocation ratio between the experimental arm "NGS" and the standard "No NGS". NGS will be considered feasible if (i) NGS results are available and interpretable, and (ii) a report of exome sequencing including a clinical recommendation from a multidisciplinary tumor board is provided to investigators within 7 weeks from reception of the samples on the biopathological platform. A feasibility rate of more than 70% is expected (null hypothesis: 70% versus alternative hypothesis: 80%). In terms of care, participants randomized in "No NGS" arm and who fail treatment will be able to switch to the NGS arm at the request of the investigator. DISCUSSION: The MULTISARC trial is a prospective study designed to provide high-level evidence to support the implementation of NGS in routine clinical practice for advanced STS participants, on a large scale. TRIAL REGISTRATION: clinicaltrial.gov NCT03784014 .
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sarcoma / Neoplasias de Tecidos Moles / Sequenciamento de Nucleotídeos em Larga Escala Tipo de estudo: Clinical_trials / Guideline / Observational_studies / Prognostic_studies / Qualitative_research Limite: Adult / Humans País/Região como assunto: Europa Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sarcoma / Neoplasias de Tecidos Moles / Sequenciamento de Nucleotídeos em Larga Escala Tipo de estudo: Clinical_trials / Guideline / Observational_studies / Prognostic_studies / Qualitative_research Limite: Adult / Humans País/Região como assunto: Europa Idioma: En Ano de publicação: 2021 Tipo de documento: Article