e17063 Background: Intraductal carcinoma of the prostate (IDC-P) is a clinicopathological entity of prostate cancer characterized by increased homologous recombination repair deficiency (HRD). This study aimed to evaluate the predictive value of IDC-P for the efficacy of olaparib combined with novel hormonal therapy (NHT) in metastatic castration-resistant prostate cancer (mCRPC) after progression on NHT. Methods: A total of 64 consecutive patients treated with olaparib plus NHT after NHT progression were analyzed, including 33 IDC-P and 31 prostate adenocarcinoma (PAC) cases. Main outcomes included progression-free survival (PFS) and treatment change-free survival (TFS). Prostate-specific antigen (PSA) response, overall survival and adverse events were also evaluated. Additionally, paired blood and tissue samples from 187 PCa patients were analyzed to assess HRD scores. Results: After a median follow-up of 35.0 months, patients with IDC-P showed significantly longer PFS and TFS than those with PAC (PFS: 6.2 vs. 3.0 months, p 0.9 3 3 (4.7%) 2 (6.5%) 1 (3.0%) 4 11 (17%) 5 (16%) 6 (18%) 5 50 (78%) 24 (77%) 26 (79%) Metastatic burden 0.02 <5 20 (31%) 14 (45%) 6 (18%) ≥5 44 (69%) 17 (55%) 27 (82%) Visceral metastasis 9 (14%) 4 (13%)
Zhu et al. (Thu,) studied this question.
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