Department of Urology, Toho University Sakura Medical Center, Chiba, Japan.
Department of Urology, Oita University Faculty of Medicine, Oita, Japan.
Jpn J Clin Oncol. 2020 Jul 9;50(7):810-820. doi: 10.1093/jjco/hyaa030.
LATITUDE was a randomized, double-blind, international and phase 3 study of abiraterone acetate plus prednisone in patients with high-risk metastatic hormone-naïve prostate cancer. In the first interim analysis of LATITUDE (clinical cutoff date: 31 October 2016), significant prolongation in overall survival and radiographic progression-free survival (co-primary endpoints) was observed when compared with placebo. The results of the Japanese subgroup analysis of LATITUDE first interim analysis were consistent with those of the overall population. In this study, overall survival and safety results from the final analysis of the Japanese subgroup of the LATITUDE study are presented (clinical cutoff date: 15 August 2018).
Abiraterone acetate (1000 mg/day) and prednisone (5 mg/day) were administered orally in the abiraterone acetate plus prednisone group, and matching placebos in the placebo group.
Of the 1199 patients included in LATITUDE, 70 constituted the Japanese subgroup (abiraterone acetate plus prednisone: n = 35, placebo: n = 35). Following a median (range) follow-up of 56.6 (2.5, 64.2) months, the median overall survival was not reached in both the treatment arms of the Japanese subgroup (hazard ratio: 0.61; 95% confidence interval: 0.27-1.42; nominal P = 0.2502). A total of 23 deaths (abiraterone acetate plus prednisone: 9 [25.7%], placebo group: 14 [40.0%]) were reported in Japanese subgroup. Grade 3/4 adverse events were reported in 24 (68.6%) and 9 (25.7%) patients in the abiraterone acetate plus prednisone and placebo groups, respectively.
In this Japanese subgroup analysis, addition of abiraterone acetate plus prednisone to androgen-deprivation therapy demonstrated favorable efficacy and safety outcomes in patients with newly diagnosed, high-risk metastatic hormone-naïve prostate cancer. Survival benefits observed in the Japanese subgroup first interim analysis were sustained long-term and were consistent with the overall population.
LATITUDE 是一项随机、双盲、国际性的 III 期研究,评估醋酸阿比特龙联合泼尼松在高危转移性去势敏感性前列腺癌患者中的疗效。在 LATITUDE 的第一次期中分析(临床截止日期:2016 年 10 月 31 日)中,与安慰剂相比,观察到总生存期和影像学无进展生存期(共同主要终点)的显著延长。LATITUDE 的日本亚组分析结果与总体人群一致。本研究报告了 LATITUDE 研究日本亚组最终分析的总生存期和安全性结果(临床截止日期:2018 年 8 月 15 日)。
醋酸阿比特龙(1000mg/天)和泼尼松(5mg/天)在醋酸阿比特龙联合泼尼松组中口服给药,在安慰剂组中给予匹配的安慰剂。
在 LATITUDE 中纳入的 1199 例患者中,70 例构成了日本亚组(醋酸阿比特龙联合泼尼松组:n=35,安慰剂组:n=35)。在日本亚组中,中位(范围)随访时间为 56.6(2.5,64.2)个月,两个治疗组的中位总生存期均未达到(风险比:0.61;95%置信区间:0.27-1.42;名义 P=0.2502)。在日本亚组中,共报告了 23 例死亡(醋酸阿比特龙联合泼尼松组:9 例[25.7%],安慰剂组:14 例[40.0%])。在醋酸阿比特龙联合泼尼松组和安慰剂组中,分别有 24 例(68.6%)和 9 例(25.7%)患者发生 3/4 级不良事件。
在这项日本亚组分析中,与单独去势治疗相比,新诊断的高危转移性去势敏感性前列腺癌患者中添加醋酸阿比特龙联合泼尼松治疗可带来有利的疗效和安全性结局。在日本亚组第一次期中分析中观察到的生存获益得到了长期维持,与总体人群一致。