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Androgen Suppression Combined with Elective Nodal and Dose Escalated Radiation Therapy (the ASCENDE-RT Trial): An Analysis of Survival Endpoints for a Randomized Trial Comparing a Low-Dose-Rate Brachytherapy Boost to a Dose-Escalated External Beam Boost for High- and Intermediate-risk Prostate Cancer.雄激素抑制联合选择性淋巴结及剂量递增放射治疗(ASCENDE-RT试验):一项针对高风险和中风险前列腺癌的随机试验的生存终点分析,该试验比较了低剂量率近距离放疗增敏与剂量递增外照射增敏。
Int J Radiat Oncol Biol Phys. 2017 Jun 1;98(2):275-285. doi: 10.1016/j.ijrobp.2016.11.026. Epub 2016 Nov 24.
2
Can we avoid high levels of dose escalation for high-risk prostate cancer in the setting of androgen deprivation?在雄激素剥夺治疗的情况下,我们能否避免对高危前列腺癌进行高强度的剂量递增?
Onco Targets Ther. 2016 May 11;9:2819-24. doi: 10.2147/OTT.S105174. eCollection 2016.
3
High-dose radiotherapy with helical tomotherapy and long-term androgen deprivation therapy for prostate cancer: 5-year outcomes.螺旋断层放疗联合长期雄激素剥夺治疗前列腺癌的大剂量放疗:5年结果
J Cancer Res Clin Oncol. 2016 Jul;142(7):1609-19. doi: 10.1007/s00432-016-2173-9. Epub 2016 May 2.
4
Can we avoid dose escalation for intermediate-risk prostate cancer in the setting of short-course neoadjuvant androgen deprivation?在短程新辅助雄激素剥夺治疗的情况下,我们能否避免对中度风险前列腺癌进行剂量递增?
Onco Targets Ther. 2016 Mar 17;9:1635-9. doi: 10.2147/OTT.S102327. eCollection 2016.
5
Weighing the Addition of Androgen Suppression Therapy to Radiotherapy Dose Escalation for Intermediate-Risk Prostate Cancer.权衡在中危前列腺癌放疗剂量递增基础上加用雄激素抑制疗法的利弊。
J Clin Oncol. 2016 May 20;34(15):1715-7. doi: 10.1200/JCO.2015.66.2320. Epub 2016 Mar 14.
6
Short Androgen Suppression and Radiation Dose Escalation for Intermediate- and High-Risk Localized Prostate Cancer: Results of EORTC Trial 22991.短程雄激素抑制联合放疗治疗中高危局限性前列腺癌:EORTC 试验 22991 结果。
J Clin Oncol. 2016 May 20;34(15):1748-56. doi: 10.1200/JCO.2015.64.8055. Epub 2016 Mar 14.
7
Current use of PSMA-PET in prostate cancer management.PSMA-PET 在前列腺癌管理中的当前应用。
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8
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J Natl Compr Canc Netw. 2016 Jan;14(1):19-30. doi: 10.6004/jnccn.2016.0004.
9
Radiation dose escalation or longer androgen suppression for locally advanced prostate cancer? Data from the TROG 03.04 RADAR trial.局部晚期前列腺癌的放疗剂量升级或更长时间的雄激素抑制?来自 TROG 03.04 RADAR 试验的数据。
Radiother Oncol. 2015 Jun;115(3):301-7. doi: 10.1016/j.radonc.2015.05.016. Epub 2015 Jun 10.
10
High-dose radiotherapy with short-term or long-term androgen deprivation in localised prostate cancer (DART01/05 GICOR): a randomised, controlled, phase 3 trial.高剂量放疗联合短期或长期雄激素剥夺治疗局限性前列腺癌(DART01/05 GICOR):一项随机、对照、3 期临床试验。
Lancet Oncol. 2015 Mar;16(3):320-7. doi: 10.1016/S1470-2045(15)70045-8. Epub 2015 Feb 19.

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.

DOI:10.1259/bjr.20170431
PMID:29166142
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5965477/
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。