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剂量递增放疗联合长期雄激素剥夺治疗对前列腺癌的影响。

Effects of dose-escalated radiotherapy in combination with long-term androgen deprivation on prostate cancer.

作者信息

Tomita Natsuo, Soga Norihito, Ogura Yuji, Furusawa Jun, Shimizu Hidetoshi, Adachi Sou, Tanaka Hiroshi, Kato Daiki, Koide Yutaro, Makita Chiyoko, Tachibana Hiroyuki, Kodaira Takeshi

机构信息

1 Department of Radiation Oncology , Aichi Cancer Center Hospital , Nagoya , Japan.

2 Department of Urology,Aichi Cancer Center Hospital , Aichi Cancer Center Hospital , Nagoya , Japan.

出版信息

Br J Radiol. 2018 Feb;91(1083):20170431. doi: 10.1259/bjr.20170431. Epub 2017 Dec 5.

Abstract

OBJECTIVE

We aimed to examine the effects of a dose escalation for prostate cancer patients receiving long-term androgen deprivation therapy (ADT).

METHODS

A retrospective analysis of 605 patients treated with radiotherapy (RT) and long-term ADT (National Comprehensive Cancer Network criteria-defined intermediate-risk, minimum 10 months; high-risk and very-high-risk, minimum 20 months) was performed. The median ADT time was 31 months. Cox's proportional hazards models were used to compare biochemical disease-free survival (bDFS), clinical relapse-free survival (cRFS) and overall survival (OS) between the ≥70, <78 Gy group and 78 Gy group in a univariate analysis and to assess the effects of the dose escalation on bDFS in a multivariate analysis.

RESULTS

After a median follow-up of 70 months, 5-year bDFS was significantly better in the 78 Gy group than in the ≥70, <78 Gy group [96 vs 83%; hazard ratio 3.6 (95% confidence interval 2.2-6.1); p < 0.001]. 5-year cRFS and OS were similar between the two groups. The multivariate analysis showed that RT dose was still an independent prognostic factor of bDFS (p = 0.005).

CONCLUSION

The results of the present study suggest that dose escalations result in significant improvements in bDFS, even when used in combination with long-term ADT. A longer follow-up is needed to clarify the effects of dose escalations on cRFS and OS. Advances in knowledge: It remains unclear whether high-dose RT is necessary for improving the outcomes of patients receiving long-term ADT. The results suggest that dose escalations result in significant improvements in biochemical control.

摘要

目的

我们旨在研究剂量递增对接受长期雄激素剥夺治疗(ADT)的前列腺癌患者的影响。

方法

对605例接受放疗(RT)和长期ADT(根据美国国立综合癌症网络标准定义为中危,至少10个月;高危和极高危,至少20个月)的患者进行回顾性分析。ADT的中位时间为31个月。采用Cox比例风险模型在单因素分析中比较≥70、<78 Gy组和78 Gy组之间的生化无病生存期(bDFS)、临床无复发生存期(cRFS)和总生存期(OS),并在多因素分析中评估剂量递增对bDFS的影响。

结果

中位随访70个月后,78 Gy组的5年bDFS显著优于≥70、<78 Gy组[96%对83%;风险比3.6(95%置信区间2.2 - 6.1);p < 0.001]。两组的5年cRFS和OS相似。多因素分析显示,放疗剂量仍是bDFS的独立预后因素(p = 0.005)。

结论

本研究结果表明,即使与长期ADT联合使用,剂量递增也能显著改善bDFS。需要更长时间的随访来阐明剂量递增对cRFS和OS的影响。知识进展:对于改善接受长期ADT患者的预后,高剂量放疗是否必要仍不清楚。结果表明剂量递增能显著改善生化控制。

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