Tomita Natsuo, Soga Norihito, Ogura Yuji, Furusawa Jun, Shimizu Hidetoshi, Adachi Sou, Tanaka Hiroshi, Kato Daiki, Koide Yutaro, Makita Chiyoko, Tachibana Hiroyuki, Kodaira Takeshi
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.
Br J Radiol. 2018 Feb;91(1083):20170431. doi: 10.1259/bjr.20170431. Epub 2017 Dec 5.
We aimed to examine the effects of a dose escalation for prostate cancer patients receiving long-term androgen deprivation therapy (ADT).
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.
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).
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.
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。
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。
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)。
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。