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Emerging PARP inhibitors for treating breast cancer
Authors:Marie Robert  Anne Patsouris  Jean-Sébastien Frenel  Carole Gourmelon  Paule Augereau  Mario Campone
Affiliation:1. René Gauducheau, Institut de Cancérologie de l’Ouest, St Herblain, FranceMarie.Robert@ico.unicancer.fr;3. Paul Papin, Institut de Cancérologie de l’Ouest, Angers, France;4. René Gauducheau, Institut de Cancérologie de l’Ouest, St Herblain, France;5. Medical oncology, Centre de Recherche en Cancérologie Nantes-Angers (CRNA), Saint-Herblain, France
Abstract:
ABSTRACT

Introduction: Some breast cancers harbor defects in DNA repair pathways, including BRCA1 and BRCA2 mutations, leading to a genomic instability. Compromised DNA-damage repair response is found in 11 to 42% of triple negative breast cancers, with a frequency varying according to family history and ethnicity. The oral PARP inhibitors are a promising strategy in breast cancer exploiting Homologous Deficient Recombination deficiency (HRD) by a synthetic lethal approach. Several PARP inhibitors have currently reached early phase trials with studies on going in the adjuvant, neoadjuvant and metastatic setting.

Area covered: Here, we review completed and ongoing trials with PARP inhibitors as well as their mechanisms of activity and acquired resistance.

Expert opinion: PARP inhibitors show promising results in breast cancer. However, several issues are raised including the identification of biomarkers to predict treatment response and strategies to counteract emerging resistance.
Keywords:Breast cancer  BRCA1/2  BRCAness  PARP inhibitors
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