Thromboembolic Events in Castration-Resistant Prostate Cancer Patients With and Without Cardiovascular Comorbidities Receiving Oral Androgen Receptor Pathway Inhibitors.

IF 2.6 3区 医学 Q3 ENDOCRINOLOGY & METABOLISM
Prostate Pub Date : 2025-07-01 Epub Date: 2025-05-01 DOI:10.1002/pros.24902
Ibrahim M Asiri, Ronald C Chen, Viraj Master, Lanyu Mi, Sarah E James, Alan H Bryce, Umar Afzal, Irbaz B Riaz, Syed Arsalan Ahmed Naqvi, Steven R H Beach, Ewan K Cobran
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Abstract

Background: This study investigates the association between thromboembolic events (TE) and castration-resistant prostate cancer (CRPC) patients receiving oral androgen receptor pathway inhibitors (ARPi) compared to those undergoing chemotherapy, both with and without a pre-existing history of cardiovascular disease (CVD).

Methods: A total of 2779 men diagnosed with CRPC were identified using the Surveillance, Epidemiology, and End Results (SEER) Medicare Linked Database from 2012 to 2016. Patients were stratified based on their CVD history. Within each CVD stratum (pre-existing CVD vs. no pre-existing CVD), patients were further categorized into two treatment groups: those receiving oral ARPi and those undergoing chemotherapy. Unadjusted and inverse probability treatment weight (IPTW)-adjusted proportional hazards models, using Fine and Gray's method, were applied to evaluate the potential association between ARPi treatment and TE.

Results: Patients with pre-existing CVD treated with ARPi exhibited a significantly lower crude hazard ratio (HR) for TE compared to chemotherapy (HR 0.39, 95% CI 0.27-0.58, p < 0.001). However, after adjustment using IPTW, this association was no longer significant (adjusted hazard ratio [AHR] 1.00, 95% CI 0.75-1.32, p = 0.99). For patients without CVD, ARPi use was also associated with a reduced risk of TE in the crude analysis (HR 0.53, 95% CI 0.32-0.87, p = 0.01), but this effect was not statistically significant after IPTW adjustment (HR 0.99, 95% CI 0.69-1.41, p = 0.94).

Conclusion: ARPi demonstrated no significant effect on TE risk compared to chemotherapy, regardless of pre-existing CVD status. Similarly, when excluding patients with a prior history of TE, ARPi use remained non-significantly associated with new TE in the IPTW-adjusted competing risk analysis, highlighting the need for further investigation.

口服雄激素受体途径抑制剂治疗有或无心血管合并症的去势抵抗性前列腺癌患者的血栓栓塞事件
背景:本研究调查了接受口服雄激素受体途径抑制剂(ARPi)和化疗的去势抵抗性前列腺癌(CRPC)患者,无论是否有心血管疾病(CVD)病史,血栓栓塞事件(TE)和去势抵抗性前列腺癌(CRPC)之间的关系。方法:2012年至2016年,通过监测、流行病学和最终结果(SEER)医疗保险关联数据库,共识别2779名诊断为CRPC的男性。根据CVD病史对患者进行分层。在每个CVD层(已存在CVD与未存在CVD)中,患者进一步分为两个治疗组:口服ARPi组和化疗组。采用Fine和Gray方法,应用未经调整和逆概率处理权(IPTW)调整的比例风险模型来评估ARPi处理与TE之间的潜在关联。结果:与化疗相比,ARPi治疗的已存在CVD患者的TE粗风险比(HR)显著降低(HR 0.39, 95% CI 0.27-0.58, p)。结论:与化疗相比,ARPi对TE风险无显著影响,无论是否存在CVD。同样,当排除有TE病史的患者时,在iptw调整后的竞争风险分析中,ARPi的使用与新发TE的相关性仍然不显著,这突出了进一步研究的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Prostate
Prostate 医学-泌尿学与肾脏学
CiteScore
5.10
自引率
3.60%
发文量
180
审稿时长
1.5 months
期刊介绍: The Prostate is a peer-reviewed journal dedicated to original studies of this organ and the male accessory glands. It serves as an international medium for these studies, presenting comprehensive coverage of clinical, anatomic, embryologic, physiologic, endocrinologic, and biochemical studies.
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