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基于合并症的恩杂鲁胺和阿比特龙治疗转移性去势抵抗性前列腺癌的退伍军人的生存情况。

Survival of veterans treated with enzalutamide and abiraterone for metastatic castrate resistant prostate cancer based on comorbid diseases.

机构信息

Saint Louis Veterans Affairs Medical Center, Saint Louis, MO, USA.

Department of Internal Medicine, Saint Louis University School of Medicine, Saint Louis, MO, USA.

出版信息

Prostate Cancer Prostatic Dis. 2023 Dec;26(4):743-750. doi: 10.1038/s41391-022-00588-5. Epub 2022 Sep 14.

Abstract

BACKGROUND

Comorbid diseases influence patient outcomes, yet little is known about how comorbidities interact with treatments for metastatic castrate-resistant prostate cancer (mCRPC). No head-to-head trials have compared the efficacy of abiraterone and enzalutamide - oral androgen-receptor targeted agents (ARTAs) for mCRPC. In patients with comorbid disease, outcomes with ARTAs may differ due to disparate mechanisms of action, adverse events, and drug interactions.

METHODS

Retrospective observational study of US veterans initiating treatment for mCRPC with abiraterone or enzalutamide between September 2014 and June 2017. Treatment duration and overall survival (OS) was compared based on age and comorbid diseases. The association between ARTA and OS was assessed using Cox proportional hazards and propensity-score matched modeling while adjusting for potential confounders. Sensitivity analyses were performed based on patient age, comorbidities, and subsequent treatments for mCRPC.

RESULTS

Of 5822 veterans treated for mCRPC, 43.0% initially received enzalutamide and 57.0% abiraterone. Veterans initially treated with enzalutamide versus abiraterone were older (mean 75.8 vs. 75.0 years) with higher mean Charlson comorbidity index (4.4 vs. 4.1), and higher rates of cardiovascular disease or diabetes (74.2% vs. 70.6%). In the entire population, veterans initially treated with enzalutamide had longer median OS compared to those initially treated with abiraterone (24.2 vs. 22.1 months, p = 0.001). In veterans with cardiovascular disease or diabetes, median treatment duration with enzalutamide was longer (11.4 vs. 8.6 months, p < 0.001) with longer median OS compared to abiraterone (23.2 vs. 20.5 months, p < 0.001). In a propensity score matched cohort, enzalutamide was associated with decreased mortality compared to abiraterone (HR 0.90, 95% CI 0.84-0.96).

CONCLUSIONS

Veterans with cardiovascular disease or diabetes had longer treatment duration and OS with enzalutamide compared to abiraterone. Further study of ARTA selection may benefit men with metastatic castrate resistant prostate cancer and likely hormone sensitive prostate cancer, especially among patients with comorbid diseases.

摘要

背景

合并症会影响患者的预后,但对于合并症如何与转移性去势抵抗性前列腺癌(mCRPC)的治疗相互作用知之甚少。尚无头对头试验比较阿比特龙和恩扎鲁胺——口服雄激素受体靶向药物(ARTAs)治疗 mCRPC 的疗效。在合并疾病的患者中,由于作用机制、不良反应和药物相互作用的不同,ARTAs 的疗效可能会有所不同。

方法

这是一项回顾性观察性研究,纳入了 2014 年 9 月至 2017 年 6 月期间接受阿比特龙或恩扎鲁胺治疗的美国退伍军人,比较了基于年龄和合并疾病的治疗持续时间和总生存期(OS)。使用 Cox 比例风险和倾向评分匹配模型评估 ARTA 与 OS 的相关性,同时调整潜在混杂因素。根据患者年龄、合并症和 mCRPC 的后续治疗进行敏感性分析。

结果

在接受 mCRPC 治疗的 5822 名退伍军人中,43.0% 最初接受恩扎鲁胺治疗,57.0% 最初接受阿比特龙治疗。与接受阿比特龙治疗的退伍军人相比,最初接受恩扎鲁胺治疗的退伍军人年龄更大(平均 75.8 岁 vs. 75.0 岁),平均 Charlson 合并症指数更高(4.4 分 vs. 4.1 分),心血管疾病或糖尿病的发生率更高(74.2% vs. 70.6%)。在整个队列中,与接受阿比特龙治疗的退伍军人相比,接受恩扎鲁胺治疗的退伍军人的中位 OS 更长(24.2 个月 vs. 22.1 个月,p=0.001)。在患有心血管疾病或糖尿病的退伍军人中,与阿比特龙相比,接受恩扎鲁胺治疗的退伍军人的中位治疗持续时间更长(11.4 个月 vs. 8.6 个月,p<0.001),中位 OS 也更长(23.2 个月 vs. 20.5 个月,p<0.001)。在倾向评分匹配队列中,与阿比特龙相比,恩扎鲁胺与死亡率降低相关(HR 0.90,95%CI 0.84-0.96)。

结论

与阿比特龙相比,患有心血管疾病或糖尿病的退伍军人接受恩扎鲁胺治疗的时间更长,OS 更长。进一步研究 ARTA 的选择可能会使患有转移性去势抵抗性前列腺癌和可能的激素敏感性前列腺癌的男性受益,尤其是患有合并症的患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49f5/10638085/18ea5a855d0f/41391_2022_588_Fig1_HTML.jpg

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