奥拉帕尼
医学
前列腺癌
内科学
不利影响
肿瘤科
阿比曲酮
卡巴齐塔塞尔
癌症
雄激素剥夺疗法
雄激素受体
生物化学
聚合酶
基因
聚ADP核糖聚合酶
化学
作者
Sijin Chen,Dewen Zhong,Chenbo Yu,Desheng Cai,Qichen Wei,Minggen Yang,Tao Li,Qingguo Zhu,Liefu Ye,Yongbao Wei,Jinfeng Wu
标识
DOI:10.1038/s41598-024-70398-3
摘要
Although overall survival data are still premature, the PROpel study found radiological progression-free survival (PFS) benefits of abiraterone and olaparib in patients with metastatic castration-resistant prostate cancer (mCRPC). However, for patients who have not been genetically tested or lack BRCA1/2 mutations (BRCAm), this combination therapy has been questioned as a first-line conventional treatment for mCRPC, mainly due to significant health economics and side effects. In our retrospective study, we found that treatment with low-dose abiraterone plus olaparib as a late-line treatment for mCRPC could lead to prostate-specific antigen (PSA) and symptom PFS in selective cases even without BRCAm. The median PSA–PFS was 8 months (IQR: 6.5–11.5), with a median follow-up duration of 39.0 months (IQR: 27.5–64.5). Gene tests were conducted in all patients, identifying non-BRCA mutations through ctDNA testing (24%), tumor tissue testing (12%), or both (64%). Adverse events occurred in 72% of patients, with 16% experiencing Grade ≥ 3 events. Common adverse events included anemia (64%), decreased appetite (48%), and fatigue (25%). Our findings support low-dose abiraterone plus olaparib as a potential option for mCRPC patients without BRCAm, offering manageable safety and efficacy profiles.
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