PARP enzymes are essential for DNA damage repair. Cancers with defective homologous recombination DNA repair, such has - and -mutated breast cancers, are targets for PARP inhibitors (PARPi) through the exploitation of synthetic lethality. A number of PARPi are currently undergoing clinical evaluation in breast cancer, with olaparib and talazoparib having demonstrated superior efficacy compared with standard chemotherapy in advanced germline -mutated cancer. This review describes the biological rationale for PARPi and presents the accumulating data on PARPi use in breast cancer.
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http://dx.doi.org/10.6004/jnccn.2018.7031 | DOI Listing |
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