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Published in: BMC Cancer 1/2021

Open Access 01-12-2021 | Soft Tissue Sarcoma | Study protocol

Molecular profiling of advanced soft-tissue sarcomas: the MULTISARC randomized trial

Authors: Antoine Italiano, Derek Dinart, Isabelle Soubeyran, Carine Bellera, Hélène Espérou, Christelle Delmas, Noémie Mercier, Sabrina Albert, Ludivine Poignie, Anne Boland, Aurélien Bourdon, Damien Geneste, Quentin Cavaille, Yec’han Laizet, Emmanuel Khalifa, Céline Auzanneau, Barbara Squiban, Nathalène Truffaux, Robert Olaso, Zuzana Gerber, Cédrick Wallet, Antoine Bénard, Jean-Yves Blay, Pierre Laurent-Puig, Jean-François Deleuze, Carlo Lucchesi, Simone Mathoulin-Pelissier, the MULTISARC study group

Published in: BMC Cancer | Issue 1/2021

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Abstract

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.
Appendix
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Literature
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Metadata
Title
Molecular profiling of advanced soft-tissue sarcomas: the MULTISARC randomized trial
Authors
Antoine Italiano
Derek Dinart
Isabelle Soubeyran
Carine Bellera
Hélène Espérou
Christelle Delmas
Noémie Mercier
Sabrina Albert
Ludivine Poignie
Anne Boland
Aurélien Bourdon
Damien Geneste
Quentin Cavaille
Yec’han Laizet
Emmanuel Khalifa
Céline Auzanneau
Barbara Squiban
Nathalène Truffaux
Robert Olaso
Zuzana Gerber
Cédrick Wallet
Antoine Bénard
Jean-Yves Blay
Pierre Laurent-Puig
Jean-François Deleuze
Carlo Lucchesi
Simone Mathoulin-Pelissier
the MULTISARC study group
Publication date
01-12-2021
Publisher
BioMed Central
Published in
BMC Cancer / Issue 1/2021
Electronic ISSN: 1471-2407
DOI
https://doi.org/10.1186/s12885-021-08878-2

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