| Literature DB >> 28365644 |
Christophe Massard1, Stefan Michiels2, Charles Ferté1, Marie-Cécile Le Deley2, Ludovic Lacroix3, Antoine Hollebecque1, Loic Verlingue1, Ecaterina Ileana4, Silvia Rosellini5, Samy Ammari6, Maud Ngo-Camus1, Rastislav Bahleda1, Anas Gazzah1, Andrea Varga1, Sophie Postel-Vinay1, Yohann Loriot1, Caroline Even7, Ingrid Breuskin7, Nathalie Auger8, Bastien Job9, Thierry De Baere10, Frederic Deschamps10, Philippe Vielh11, Jean-Yves Scoazec8, Vladimir Lazar12, Catherine Richon13, Vincent Ribrag14, Eric Deutsch15, Eric Angevin1, Gilles Vassal16, Alexander Eggermont17, Fabrice André18, Jean-Charles Soria19.
Abstract
High-throughput genomic analyses may improve outcomes in patients with advanced cancers. MOSCATO 01 is a prospective clinical trial evaluating the clinical benefit of this approach. Nucleic acids were extracted from fresh-frozen tumor biopsies and analyzed by array comparative genomic hybridization, next-generation sequencing, and RNA sequencing. The primary objective was to evaluate clinical benefit as measured by the percentage of patients presenting progression-free survival (PFS) on matched therapy (PFS2) 1.3-fold longer than the PFS on prior therapy (PFS1). A total of 1,035 adult patients were included, and a biopsy was performed in 948. An actionable molecular alteration was identified in 411 of 843 patients with a molecular portrait. A total of 199 patients were treated with a targeted therapy matched to a genomic alteration. The PFS2/PFS1 ratio was >1.3 in 33% of the patients (63/193). Objective responses were observed in 22 of 194 patients (11%; 95% CI, 7%-17%), and median overall survival was 11.9 months (95% CI, 9.5-14.3 months).Significance: This study suggests that high-throughput genomics could improve outcomes in a subset of patients with hard-to-treat cancers. Although these results are encouraging, only 7% of the successfully screened patients benefited from this approach. Randomized trials are needed to validate this hypothesis and to quantify the magnitude of benefit. Expanding drug access could increase the percentage of patients who benefit. Cancer Discov; 7(6); 586-95. ©2017 AACR.See related commentary by Schram and Hyman, p. 552This article is highlighted in the In This Issue feature, p. 539. ©2017 American Association for Cancer Research.Entities:
Mesh:
Year: 2017 PMID: 28365644 DOI: 10.1158/2159-8290.CD-16-1396
Source DB: PubMed Journal: Cancer Discov ISSN: 2159-8274 Impact factor: 39.397