Onozawa Mizuki, Hinotsu Shiro, Saito Atsushi, Uno Satoshi, Akaza Hideyuki
Dept. of Urology, International University of Health and Welfare Narita Hospital.
Gan To Kagaku Ryoho. 2021 Jul;48(7):911-919.
To investigate the real-world use of primary androgen-deprivation therapy(PADT; gonadotropin-releasing hormone agonists[leuprorelin/goserelin]and antagonists[degarelix]/surgical castration), its clinical effectiveness, and the characteristics of Japanese patients with hormone-sensitive prostate cancer treated with PADT.
In this retrospective, observational study, patients using PADT(≥1 record)in the 2016-2018 Japan Study Group of Prostate Cancer registry were followed up from their initial date of PADT until October 2018. The primary endpoints included prostate-specific antigen( PSA)response rate(PSA<4 ng/mL)and duration of initial treatment.
Of 1,895 patients, 47.7%, 24.4%, and 22.0% received leuprorelin, goserelin, and degarelix, respectively; 5.9% underwent surgical castration. The degarelix group had the highest median PSA at diagnosis(116.7 ng/mL)and proportion of patients with clinical Stage Ⅳ prostate cancer (72.9%)and Gleason score 9-10(59.7%). A concomitant antiandrogen was used in >80% and 70% of patients in the leuprorelin/goserelin and degarelix groups, respectively; bicalutamide was used most commonly(99.0%). Median duration of initial treatment was 20.8 months in the degarelix group and not yet reached in the leuprorelin/goserelin groups; continuation rates at 24 months were 44.6% and 81.6%/87.3%, respectively. The PSA response rate was the highest in the leuprorelin group(93.7%); median percentage change in PSA was comparable across all treatment groups(-99.1% to -99.8%).
Real-world use of PADT in patients with hormone-sensitive prostate cancer is likely based on its specific therapeutic attributes and patient characteristics.
探讨一线雄激素剥夺治疗(PADT;促性腺激素释放激素激动剂[亮丙瑞林/戈舍瑞林]和拮抗剂[地加瑞克]/手术去势)在现实世界中的应用情况、其临床疗效以及接受PADT治疗的日本激素敏感性前列腺癌患者的特征。
在这项回顾性观察研究中,对2016 - 2018年日本前列腺癌研究组登记处使用PADT(≥1条记录)的患者从其开始接受PADT治疗之日起随访至2018年10月。主要终点包括前列腺特异性抗原(PSA)反应率(PSA<4 ng/mL)和初始治疗持续时间。
1895例患者中,分别有47.7%、24.4%和22.0%接受了亮丙瑞林、戈舍瑞林和地加瑞克治疗;5.9%接受了手术去势。地加瑞克组诊断时的中位PSA最高(116.7 ng/mL),临床Ⅳ期前列腺癌患者比例(72.9%)和 Gleason评分9 - 10分的患者比例(59.7%)最高。亮丙瑞林/戈舍瑞林组和地加瑞克组分别有超过80%和70%的患者同时使用抗雄激素药物;最常用的是比卡鲁胺(99.0%)。地加瑞克组初始治疗的中位持续时间为20.8个月,亮丙瑞林/戈舍瑞林组尚未达到;24个月时的持续治疗率分别为44.6%和81.6%/87.3%。亮丙瑞林组的PSA反应率最高(93.7%);所有治疗组的PSA中位变化百分比相当(-99.1%至-99.8%)。
激素敏感性前列腺癌患者在现实世界中使用PADT可能基于其特定的治疗属性和患者特征。