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多西他赛化疗联合雄激素抑制和放疗治疗局限性高危前列腺癌的效果:NRG 肿瘤学 RTOG 0521 随机 III 期试验。

Effect of Chemotherapy With Docetaxel With Androgen Suppression and Radiotherapy for Localized High-Risk Prostate Cancer: The Randomized Phase III NRG Oncology RTOG 0521 Trial.

机构信息

1 Sutter Medical Group and Sutter Cancer Centers, Sacramento, CA.

2 NRG Oncology Statistics and Data Management Center, Philadelphia, PA.

出版信息

J Clin Oncol. 2019 May 10;37(14):1159-1168. doi: 10.1200/JCO.18.02158. Epub 2019 Mar 12.

Abstract

PURPOSE

Radiotherapy (RT) plus long-term androgen suppression (AS) are a standard treatment option for patients with high-risk localized prostate cancer. We hypothesized that docetaxel chemotherapy (CT) could improve overall survival (OS) and clinical outcomes among patients with high-risk prostate cancer.

PATIENTS AND METHODS

The multicenter randomized NRG Oncology RTOG 0521 study enrolled patients with high-risk nonmetastatic disease between 2005 and 2009. Patients were randomly assigned to receive standard long-term AS plus RT with or without adjuvant CT.

RESULTS

A total of 612 patients were enrolled; 563 were evaluable. Median prostate-specific antigen was 15.1 ng/mL; 53% had a Gleason score 9 to 10 cancer; 27% had cT3 to cT4 disease. Median follow-up was 5.7 years. Treatment was well tolerated in both arms. Four-year OS rate was 89% (95% CI, 84% to 92%) for AS + RT and 93% (95% CI, 90% to 96%) for AS + RT + CT (hazard ratio [HR], 0.69; 90% CI, 0.49 to 0.97; one-sided = .034). There were 59 deaths in the AS + RT arm and 43 in the AS + RT + CT arm, with fewer deaths resulting from prostate cancer in the AS + RT + CT arm versus AS + RT (23 16 deaths, respectively). Six-year rate of distant metastasis was 14% for AS + RT and 9.1% for AS + RT + CT, (HR, 0.60; 95% CI, 0.37 to 0.99; two-sided = .044). Six-year disease-free survival rate was 55% for AS + RT and 65% for AS + RT + CT (HR, 0.76; 95% CI, 0.58 to 0.99; two-sided = .043).

CONCLUSION

For patients with high-risk nonmetastatic prostate cancer, CT with docetaxel improved OS from 89% to 93% at 4 years, with improved disease-free survival and reduction in the rate of distant metastasis. The trial suggests that docetaxel CT may be an option to be discussed with selected men with high-risk prostate cancer.

摘要

目的

放疗(RT)加长期雄激素抑制(AS)是高危局限性前列腺癌患者的标准治疗选择。我们假设多西他赛化疗(CT)可以改善高危前列腺癌患者的总生存期(OS)和临床结局。

患者和方法

NRG Oncology RTOG 0521 多中心随机研究纳入了 2005 年至 2009 年间患有高危非转移性疾病的患者。患者被随机分配接受标准的长期 AS 加 RT 加或不加辅助 CT。

结果

共纳入 612 例患者;563 例可评估。中位前列腺特异性抗原为 15.1ng/ml;53%的患者有 Gleason 评分 9 至 10 分的癌症;27%的患者有 cT3 至 cT4 疾病。中位随访时间为 5.7 年。两种治疗方法均耐受良好。AS+RT 组的 4 年 OS 率为 89%(95%CI,84%至 92%),AS+RT+CT 组为 93%(95%CI,90%至 96%)(风险比[HR],0.69;90%CI,0.49 至 0.97;单侧=0.034)。AS+RT 组有 59 例死亡,AS+RT+CT 组有 43 例死亡,AS+RT+CT 组死于前列腺癌的死亡人数少于 AS+RT 组(分别为 23 例和 16 例)。AS+RT 组的远处转移 6 年发生率为 14%,AS+RT+CT 组为 9.1%(HR,0.60;95%CI,0.37 至 0.99;双侧=0.044)。AS+RT 组的无病生存期为 55%,AS+RT+CT 组为 65%(HR,0.76;95%CI,0.58 至 0.99;双侧=0.043)。

结论

对于患有高危非转移性前列腺癌的患者,多西他赛 CT 可将 4 年时的 OS 从 89%提高到 93%,改善无病生存率并降低远处转移率。该试验表明,多西他赛 CT 可能是与高危前列腺癌患者讨论的选择之一。

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