Princess Margaret Cancer Centre, Toronto, Canada; Faculty of Medicine, University of New South Wales, Kensington, Australia; Kinghorn Cancer Centre, St Vincents Hospital, Darlinghurst, Sydney, Australia.
Duke Cancer Institute Center for Prostate and Urologic Cancers, Durham NC, USA.
Eur J Cancer. 2022 Jul;170:296-304. doi: 10.1016/j.ejca.2022.03.042. Epub 2022 May 11.
The associations of metformin and statins with overall survival (OS) and prostate specific antigen response rate (PSA-RR) in trials in metastatic castration-resistant prostate cancer remain unclear.
To determine whether metformin or statins ± abiraterone acetate plus prednisone/prednisolone (AAP) influence OS and PSA-RR.
DESIGN, SETTING AND PARTICIPANT: COU-AA-301 and COU-AA-302 patients were stratified by metformin and statin use. Cox proportional hazards models were used to estimate hazards ratio (HR) stratified by concomitant medications, and a random effects model was used to pool HR. We compared PSA-RR using Chi χ test.
In COU-AA-301-AAP, metformin was associated with improved PSA-RR (41.1% versus 28.6%) but not prolonged OS. In COU-AA-301-placebo-P, there was no association between metformin and prolonged OS or PSA-RR. In COU-AA-302-AAP, metformin was associated with prolonged OS (adjHR 0.69, 95% CI 0.48-0.98) and improved PSA-RR (72.7% versus 60.0%). In COU-AA-302-P, metformin was associated with prolonged OS (adjHR 0.66, 95% CI 0.47-0.93). In pooled analysis, OS was prolonged among those treated with metformin (pooled HR 0.77, 95% CI 0.62-0.95).In COU-AA-301-AAP, statins were associated with an improved OS (adjHR 0.76, 95% CI 0.62-0.93), while there was no difference in COU-AA-301-P. There was no association with statins and OS in either COU-AA-302 groups. When pooling HR, OS was prolonged among those treated with statins (pooled HR 0.78, 95% CI 0.68-0.88).
Within the limitations of post-hoc sub-analyses, metformin and statins are associated with a prolonged OS and increased PSA-RR, particularly in combination with AAP.
在转移性去势抵抗性前列腺癌的临床试验中,二甲双胍和他汀类药物与总生存期(OS)和前列腺特异性抗原反应率(PSA-RR)的关系仍不清楚。
确定二甲双胍或他汀类药物联合使用是否会影响 OS 和 PSA-RR。
设计、地点和参与者:COU-AA-301 和 COU-AA-302 患者按是否使用二甲双胍和他汀类药物进行分层。采用 Cox 比例风险模型估计同时使用药物的风险比(HR),并采用随机效应模型对 HR 进行合并。我们使用 Chi χ检验比较 PSA-RR。
在 COU-AA-301-AAP 中,与使用安慰剂相比,二甲双胍与 PSA-RR 的改善相关(41.1% vs. 28.6%),但与 OS 无关。在 COU-AA-301-P 中,二甲双胍与 OS 或 PSA-RR 无关。在 COU-AA-302-AAP 中,与安慰剂相比,二甲双胍与 OS 和 PSA-RR 的改善相关(调整 HR 分别为 0.69,95%CI 0.48-0.98 和 72.7% vs. 60.0%)。在 COU-AA-302-P 中,二甲双胍与 OS 相关(调整 HR 为 0.66,95%CI 0.47-0.93)。在合并分析中,使用二甲双胍的患者 OS 延长(合并 HR 为 0.77,95%CI 0.62-0.95)。在 COU-AA-301-AAP 中,他汀类药物与 OS 改善相关(调整 HR 为 0.76,95%CI 0.62-0.93),而在 COU-AA-301-P 中无差异。在 COU-AA-302 两组中,他汀类药物与 OS 无关。在合并 HR 分析中,使用他汀类药物的患者 OS 延长(合并 HR 为 0.78,95%CI 0.68-0.88)。
在事后亚分析的限制范围内,二甲双胍和他汀类药物与 OS 延长和 PSA-RR 增加相关,尤其是与 AAP 联合使用时。