Risk of major adverse cardiovascular events among second-line hormonal therapy for metastatic castration-resistant prostate cancer: A real-world evidence study

被引:12
作者
Liu, Jui-Ming [1 ,2 ]
Lin, Cheng-Chia [3 ]
Chen, Miao-Fen [4 ,5 ]
Liu, Kuan-Lin [3 ]
Lin, Cheng-Feng [3 ]
Chen, Tien-Hsing [4 ,6 ,7 ]
Wu, Chun-Te [3 ,4 ]
机构
[1] Minist Hlth & Welf, Taoyuan Gen Hosp, Div Urol, Dept Surg, Taoyuan, Taiwan
[2] Natl Def Med Ctr, Grad Inst Life Sci, Taipei, Taiwan
[3] Chang Gung Mem Hosp, Dept Urol, Keelung, Taiwan
[4] Chang Gung Univ, Coll Med, Taoyuan, Taiwan
[5] Chang Gung Mem Hosp Chiayi, Dept Radiat Oncol, Chiayi, Taiwan
[6] Chang Gung Mem Hosp, Dept Med Res & Dev, Keelung, Taiwan
[7] Chang Gung Mem Hosp, Div Cardiol, Dept Internal Med, Keelung, Taiwan
关键词
abiraterone acetate; castration‐ resistant prostate cancer; Chang Gung Research Database; enzalutamide; major adverse cardiovascular events; ANDROGEN-DEPRIVATION THERAPY; ARTERIAL STIFFNESS; INCREASED SURVIVAL; HEART-FAILURE; ABIRATERONE; ENZALUTAMIDE; MEN; TESTOSTERONE; DISEASE; STROKE;
D O I
10.1002/pros.24096
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background To evaluate the possible major adverse cardiovascular events (MACE) associated with second-line hormonal therapy in patients with metastatic castration-resistant prostate cancer (mCRPC). Methods We performed a population-based real-world cohort study of 4962 prostate cancer patients between 2014 and 2017 utilizing the Chang Gung Research Database of Taiwan. The second-line hormonal therapies included enzalutamide and abiraterone acetate. The outcomes of interest were MACE, including acute coronary syndrome (ACS), ischemic stroke (IS), and heart failure (HF) events that resulted in hospitalization. Cox proportional-hazards models with inverse probability of treatment weighting (IPTW) with propensity scores were used. Results After IPTW, 288 patients were prescribed second-line hormonal therapy and 1575 received first-line androgen-deprivation therapy (ADT). Of all patients diagnosed with MACE, the event rates were 2.92% in the second-line hormonal group and 2.22% in the first-line ADT group. The mean follow-up period was 9.52 months for the second-line hormonal group. Patients who received second-line hormonal therapy exhibited a significantly increased risk for MACE (hazard ratio [HR]: 3.15; 95% confidence interval [CI]: 2.03-4.89), ACS (HR: 4.94; 95% CI: 2.36-10.33), and HF (HR: 2.83; 95% CI: 1.53-5.25), compared with the first-line ADT group, but a similar risk for IS was observed in both groups (HR: 1.70; 95% CI: 0.95-3.04). Conclusions The real-world evidence study revealed increased risks for MACE in mCRPC patients receiving second-line hormonal therapy.
引用
收藏
页码:194 / 201
页数:8
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