Actionable molecular alterations in advanced gynaecologic malignancies: updated results from the ProfiLER programme.


Journal

European journal of cancer (Oxford, England : 1990)
ISSN: 1879-0852
Titre abrégé: Eur J Cancer
Pays: England
ID NLM: 9005373

Informations de publication

Date de publication:
09 2019
Historique:
received: 02 03 2019
revised: 05 06 2019
accepted: 15 06 2019
pubmed: 28 7 2019
medline: 9 6 2020
entrez: 28 7 2019
Statut: ppublish

Résumé

The objectives of this study were to identify actionable genomic alterations in the gynaecological subpopulation of the ProfiLER programme and to report clinical efficacy of recommended targeted treatment (RTT). The ProfiLER programme (NCT01774409) is a multicentric prospective trial aiming to implement molecular profiling in patients with advanced refractory cancers. In this programme, tumour DNA is analysed by targeted next-generation sequencing (69 genes) and by whole genome array comparative genomic hybridisation. Clinical cases and genomic profiles are presented in a dedicated molecular tumour board to guide treatment strategies. We report here an analysis of patients with gynaecological cancers included in this trial. From February 2013 to February 2017, 309 patients with gynaecologic cancer were included; 279 (90%) had sufficient quality, and 131 patients (42.4%) had at least one actionable genomic alteration in cancer cells. Four alterations were shared by at least 3% of the patients: 27 (9.7%) PIK3CA mutations, 15 (5.4%) KRAS mutations, 11 (3.9%) ERBB2 amplifications and 9 (3.2%) CDKN2A deletions. Forty-one treatments were initiated among 39 patients (12.6% of the screened population): 8 (20%) had a partial response, and other 10 (24%) had a stable disease. The median progression-free survival was 2.7 months. The median overall survival was 15.6 months for patients who received a RTT. Molecular profiling identified actionable alterations in 42.4% of patients with advanced refractory gynaecologic cancer, but only 12.6% were treated with a RTT. Among them, 46% derived clinical benefit (5.8% of the screened population).

Identifiants

pubmed: 31351267
pii: S0959-8049(19)30385-5
doi: 10.1016/j.ejca.2019.06.017
pii:
doi:

Substances chimiques

Biomarkers, Tumor 0

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

156-165

Informations de copyright

Copyright © 2019 Elsevier Ltd. All rights reserved.

Auteurs

Romain Varnier (R)

Medical Practices Evaluation Team - HESPER EA7425, Centre Léon Bérard, Lyon, France; Université Claude Bernard Lyon 1, Lyon, France.

Olivia Le Saux (O)

Department of Medical Oncology, Centre Léon Bérard, Lyon, France.

Sylvie Chabaud (S)

Department of Clinical Research, Centre Léon Bérard, Lyon, France.

Gwenaëlle Garin (G)

Department of Clinical Research, Centre Léon Bérard, Lyon, France.

Emilie Sohier (E)

Department of Translational Research, Centre Léon Bérard, Lyon, France; Synergie Lyon Cancer, Plateforme de Bioinformatique 'Gilles Thomas', Centre Léon Bérard, Lyon, France.

Qing Wang (Q)

Department of Translational Research, Centre Léon Bérard, Lyon, France.

Sandrine Paindavoine (S)

Synergie Lyon Cancer, Plateforme de Bioinformatique 'Gilles Thomas', Centre Léon Bérard, Lyon, France.

David Pérol (D)

Department of Clinical Research, Centre Léon Bérard, Lyon, France.

Christian Baudet (C)

Department of Translational Research, Centre Léon Bérard, Lyon, France; Synergie Lyon Cancer, Plateforme de Bioinformatique 'Gilles Thomas', Centre Léon Bérard, Lyon, France.

Valéry Attignon (V)

Department of Translational Research, Centre Léon Bérard, Lyon, France.

Daniel Pissaloux (D)

Université Claude Bernard Lyon 1, Lyon, France; Department of Biopathology, Centre Léon Bérard, Lyon, France.

Pierre Heudel (P)

Department of Medical Oncology, Centre Léon Bérard, Lyon, France.

Benoit You (B)

Université Claude Bernard Lyon 1, Lyon, France; CITOHL, IC-HCL, Hospices Civils de Lyon, Université Claude Bernard Lyon 1, Lyon, France.

Cécile Leyronnas (C)

Department of Medical Oncology, Institut Daniel Hollard, Grenoble, France.

Olivier Collard (O)

Department of Medical Oncology, Institut Lucien Neuwirth, Saint-Priest-En-Jarez, France.

Olivier Trédan (O)

Department of Medical Oncology, Centre Léon Bérard, Lyon, France.

Nathalie Bonnin (N)

CITOHL, IC-HCL, Hospices Civils de Lyon, Université Claude Bernard Lyon 1, Lyon, France.

Jérôme Long (J)

Department of Medical Oncology, Institut Daniel Hollard, Grenoble, France.

Jean-Philippe Jacquin (JP)

Department of Medical Oncology, Institut Lucien Neuwirth, Saint-Priest-En-Jarez, France.

Philippe A Cassier (PA)

Department of Medical Oncology, Centre Léon Bérard, Lyon, France.

Olfa Derbel (O)

Department of Medical Oncology, Centre Léon Bérard, Lyon, France; Department of Medical Oncology, Hôpital Privé Jean Mermoz, Lyon, France.

Gilles Freyer (G)

Université Claude Bernard Lyon 1, Lyon, France; CITOHL, IC-HCL, Hospices Civils de Lyon, Université Claude Bernard Lyon 1, Lyon, France.

Alain Viari (A)

Synergie Lyon Cancer, Plateforme de Bioinformatique 'Gilles Thomas', Centre Léon Bérard, Lyon, France; INRIA Grenoble Rhône-Alpes, Montbonnot Saint-Martin, France.

Jean-Yves Blay (JY)

Université Claude Bernard Lyon 1, Lyon, France; Department of Medical Oncology, Centre Léon Bérard, Lyon, France.

Isabelle Ray-Coquard (I)

Medical Practices Evaluation Team - HESPER EA7425, Centre Léon Bérard, Lyon, France; Université Claude Bernard Lyon 1, Lyon, France; Department of Medical Oncology, Centre Léon Bérard, Lyon, France. Electronic address: isabelle.ray-coquard@lyon.unicancer.fr.

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Classifications MeSH