Previous Page  40 / 40
Information
Show Menu
Previous Page 40 / 40
Page Background

BRCAmut is the best biomarker to predict the highest benefit of PARP inhibitors

HRD tests can select patients BRCAwt with a longer PFS, but PARP inhibitors can

benefit any patient with HGSOC independently of biomarkers

Olaparib, Niraparib and Rucaparib improve PFS significantly as maintenance after

platinum in BRCAmut patients, and to a lesser extent in BRCAwt patients

There are a class toxicity of PARP inhibitors: asthenia, anemia, and nausea

With Niraparib, in patients <77 Kg or <150.000 platelets it is recommended a

starting dose of 200 mg/day to reduce the risk of thrombocitopenia

Rucaparib needs to be monitored for possible hepatotoxicity

There is a sinergy between PARP inhbitors and immunotherapy or antiangiogenic,

pending to confirm in phase III studies

Maintenance with PARP inhibitors in ovarian cancer

Take home messages