We tested in vivo efficacy of the combination therapy in two PDXs of BLBC origin with pathogenic BRCA1 alterations: BRCA1 R1443* mutation and truncating BRCA1 2080delA mutation...each model was treated with daily gavage of 50 mg/kg olaparib (a PARP inhibitor) and 25 mg/kg fadraciclib...The combination of CDK2 inhibition with PARP inhibition leads to tumor regression and improved survival in BRCA1 mutant PDX models.