TY - JOUR
T1 - High-throughput genomics and clinical outcome in hard-to-treat advanced cancers
T2 - Results of the MOSCATO 01 trial
AU - Massard, Christophe
AU - Michiels, Stefan
AU - Ferté, Charles
AU - Le Deley, Marie Cécile
AU - Lacroix, Ludovic
AU - Hollebecque, Antoine
AU - Verlingue, Loic
AU - Ileana, Ecaterina
AU - Rosellini, Silvia
AU - Ammari, Samy
AU - Ngo-Camus, Maud
AU - Bahleda, Rastislav
AU - Gazzah, Anas
AU - Varga, Andrea
AU - Postel-Vinay, Sophie
AU - Loriot, Yohann
AU - Even, Caroline
AU - Breuskin, Ingrid
AU - Auger, Nathalie
AU - Job, Bastien
AU - De Baere, Thierry
AU - Deschamps, Frederic
AU - Vielh, Philippe
AU - Scoazec, Jean Yves
AU - Lazar, Vladimir
AU - Richon, Catherine
AU - Ribrag, Vincent
AU - Deutsch, Eric
AU - Angevin, Eric
AU - Vassal, Gilles
AU - Eggermont, Alexander
AU - André, Fabrice
AU - Soria, Jean Charles
N1 - Publisher Copyright:
© 2017 AACR.
PY - 2017
Y1 - 2017
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85020241056&partnerID=8YFLogxK
U2 - 10.1158/2159-8290.CD-16-1396
DO - 10.1158/2159-8290.CD-16-1396
M3 - Article
C2 - 28365644
AN - SCOPUS:85020241056
SN - 2159-8274
VL - 7
SP - 586
EP - 595
JO - Cancer Discovery
JF - Cancer Discovery
IS - 6
ER -