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阿比特龙联合泼尼松治疗转移性去势敏感性前列腺癌。

Abiraterone plus Prednisone in Metastatic, Castration-Sensitive Prostate Cancer.

机构信息

From Gustave Roussy, University of Paris Sud, Villejuif, France (K.F.); Janssen Research and Development, Los Angeles (N.T.), Beerse, Belgium (P.D.P.), San Diego, CA (T.K.), and Raritan, NJ (Y.C.P.); Instituto de Oncologia de Rosário, Rosário, Argentina (L.F.); National Cancer Center Hospital East, Chiba, Japan (N.M.); 12 de Octubre University Hospital, Madrid (A.R.-A.); P.A. Hertsen Moscow Cancer Research Institute, Moscow (B.Y.A.); Cerrahpaşa Medical Faculty, Istanbul University, Istanbul, Turkey (M.Ö.); Fudan University Shanghai Cancer Center, Shanghai, China (D.Y.); Studienpraxis Urologie, Nürtingen, Germany (S.F.); Oxford University Hospitals Foundation NHS Trust, Oxford, United Kingdom (A.P.); Janssen Global Services, Raritan, NJ (M.B.T.); and BC Cancer Agency, Vancouver, Canada (K.N.C.).

出版信息

N Engl J Med. 2017 Jul 27;377(4):352-360. doi: 10.1056/NEJMoa1704174. Epub 2017 Jun 4.

Abstract

BACKGROUND

Abiraterone acetate, a drug that blocks endogenous androgen synthesis, plus prednisone is indicated for metastatic castration-resistant prostate cancer. We evaluated the clinical benefit of abiraterone acetate plus prednisone with androgen-deprivation therapy in patients with newly diagnosed, metastatic, castration-sensitive prostate cancer.

METHODS

In this double-blind, placebo-controlled, phase 3 trial, we randomly assigned 1199 patients to receive either androgen-deprivation therapy plus abiraterone acetate (1000 mg daily, given once daily as four 250-mg tablets) plus prednisone (5 mg daily) (the abiraterone group) or androgen-deprivation therapy plus dual placebos (the placebo group). The two primary end points were overall survival and radiographic progression-free survival.

RESULTS

After a median follow-up of 30.4 months at a planned interim analysis (after 406 patients had died), the median overall survival was significantly longer in the abiraterone group than in the placebo group (not reached vs. 34.7 months) (hazard ratio for death, 0.62; 95% confidence interval [CI], 0.51 to 0.76; P<0.001). The median length of radiographic progression-free survival was 33.0 months in the abiraterone group and 14.8 months in the placebo group (hazard ratio for disease progression or death, 0.47; 95% CI, 0.39 to 0.55; P<0.001). Significantly better outcomes in all secondary end points were observed in the abiraterone group, including the time until pain progression, next subsequent therapy for prostate cancer, initiation of chemotherapy, and prostate-specific antigen progression (P<0.001 for all comparisons), along with next symptomatic skeletal events (P=0.009). These findings led to the unanimous recommendation by the independent data and safety monitoring committee that the trial be unblinded and crossover be allowed for patients in the placebo group to receive abiraterone. Rates of grade 3 hypertension and hypokalemia were higher in the abiraterone group.

CONCLUSIONS

The addition of abiraterone acetate and prednisone to androgen-deprivation therapy significantly increased overall survival and radiographic progression-free survival in men with newly diagnosed, metastatic, castration-sensitive prostate cancer. (Funded by Janssen Research and Development; LATITUDE ClinicalTrials.gov number, NCT01715285 .).

摘要

背景

醋酸阿比特龙是一种阻断内源性雄激素合成的药物,联合泼尼松用于治疗转移性去势抵抗性前列腺癌。我们评估了醋酸阿比特龙联合泼尼松与雄激素剥夺疗法联合用于新诊断的转移性去势敏感性前列腺癌患者的临床获益。

方法

在这项双盲、安慰剂对照的 3 期临床试验中,我们将 1199 例患者随机分为两组:一组接受雄激素剥夺疗法加醋酸阿比特龙(1000mg 每日,每日一次给予 4 片 250mg 片剂)加泼尼松(5mg 每日)(阿比特龙组);另一组接受雄激素剥夺疗法加双安慰剂(安慰剂组)。主要终点为总生存期和影像学无进展生存期。

结果

在计划的中期分析(406 例患者死亡后)中位随访 30.4 个月后,阿比特龙组的中位总生存期明显长于安慰剂组(未达到 vs. 34.7 个月)(死亡风险比,0.62;95%置信区间[CI],0.51 至 0.76;P<0.001)。阿比特龙组的影像学无进展生存期中位长度为 33.0 个月,安慰剂组为 14.8 个月(疾病进展或死亡的风险比,0.47;95%CI,0.39 至 0.55;P<0.001)。在所有次要终点中,阿比特龙组的结果均明显更好,包括疼痛进展时间、随后前列腺癌治疗、化疗开始和前列腺特异性抗原进展(所有比较 P<0.001),以及随后的症状性骨骼事件(P=0.009)。这些发现导致独立数据和安全监测委员会一致建议试验揭盲,并允许安慰剂组患者交叉接受阿比特龙治疗。阿比特龙组的 3 级高血压和低钾血症发生率较高。

结论

醋酸阿比特龙联合泼尼松与雄激素剥夺疗法联合使用可显著提高新诊断的转移性去势敏感性前列腺癌患者的总生存期和影像学无进展生存期。(由杨森研发资助;LATITUDE 临床试验.gov 编号,NCT01715285)。

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