Abstract

PARP inhibitors (PARPi) have shown significant benefits in cancer patients with deficient homologous recombination repair (HRD; induced by BRCA mutations for example). However, they show no or very limited efficacy in tumors with active or proficient homologous recombination repair (HRP). In the current study, we propose a novel therapeutic strategy, based on drug combination to achieve synthetic lethality independently of the tumor genetics.

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