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Revisited analysis of a SHIVA01 trial cohort using functional mutational analyses successfully predicted treatment outcome.
Kamal, Maud; Tarcic, Gabi; Dureau, Sylvain; Edelheit, Oded; Barbash, Zohar; Lecerf, Charlotte; Morel, Claire; Miron, Benjamin; Callens, Celine; Servant, Nicolas; Bieche, Ivan; Vidne, Michael; Le Tourneau, Christophe.
Afiliación
  • Kamal M; Department of Drug Development and Innovation, Institut Curie, Paris & Saint-Cloud, France.
  • Tarcic G; NovellusDx, Jerusalem, Israel.
  • Dureau S; Department of Biostatistics, Institut Curie, Paris, France.
  • Edelheit O; NovellusDx, Jerusalem, Israel.
  • Barbash Z; NovellusDx, Jerusalem, Israel.
  • Lecerf C; Department of Drug Development and Innovation, Institut Curie, Paris & Saint-Cloud, France.
  • Morel C; Department of Drug Development and Innovation, Institut Curie, Paris & Saint-Cloud, France.
  • Miron B; NovellusDx, Jerusalem, Israel.
  • Callens C; Department of genetics, Institut Curie, Paris, France.
  • Servant N; Institut Curie/INSERM U900, Saint-Cloud, France.
  • Bieche I; Department of genetics, Institut Curie, Paris, France.
  • Vidne M; NovellusDx, Jerusalem, Israel.
  • Le Tourneau C; Department of Drug Development and Innovation, Institut Curie, Paris & Saint-Cloud, France.
Mol Oncol ; 12(5): 594-601, 2018 05.
Article en En | MEDLINE | ID: mdl-29464843
It still remains to be demonstrated that using molecular profiling to guide therapy improves patient outcome in oncology. Classification of somatic variants is not straightforward, rendering treatment decisions based on variants with unknown significance (VUS) hard to implement. The oncogenic activity of VUS and mutations identified in 12 patients treated with molecularly targeted agents (MTAs) in the frame of SHIVA01 trial was assessed using Functional Annotation for Cancer Treatment (FACT). MTA response prediction was measured in vitro, blinded to the actual clinical trial results, and survival predictions according to FACT were correlated with the actual PFS of SHIVA01 patients. Patients with positive prediction had a median PFS of 5.8 months versus 1.7 months in patients with negative prediction (P < 0.05). Our results highlight the role of the functional interpretation of molecular profiles to predict MTA response.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Análisis Mutacional de ADN Tipo de estudio: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Mol Oncol Asunto de la revista: BIOLOGIA MOLECULAR / NEOPLASIAS Año: 2018 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Análisis Mutacional de ADN Tipo de estudio: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Mol Oncol Asunto de la revista: BIOLOGIA MOLECULAR / NEOPLASIAS Año: 2018 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Estados Unidos