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联合放疗和雄激素剥夺治疗在中危前列腺癌中的作用:来自前列腺癌 DEGRO 工作组的声明。

Role of combined radiation and androgen deprivation therapy in intermediate-risk prostate cancer : Statement from the DEGRO working group on prostate cancer.

机构信息

Department of Radiation Oncology, Charité Universitätsmedizin Berlin, Augustenburger Platz 1, 13353, Berlin, Germany.

Department of Radiation Oncology, Inselspital, University of Bern, Bern, Switzerland.

出版信息

Strahlenther Onkol. 2020 Feb;196(2):109-116. doi: 10.1007/s00066-019-01553-3. Epub 2019 Nov 29.

DOI:10.1007/s00066-019-01553-3
PMID:31784804
Abstract

OBJECTIVE

This article aims to provide an overview of the role of combined radiation and androgen deprivation (ADT) therapy in patients with intermediate-risk prostate cancer.

MATERIALS AND METHODS

The current German, European, and NCCN (National Comprehensive Cancer Network) guidelines as well as relevant literature in the PubMed database which provide information on sub-classification within the intermediate-risk group and the use of ADT in terms of oncological outcome were reviewed.

RESULTS

Different recommendations for risk-group assessment of patients with localized prostate cancer are available. Subdivision of intermediate risk into a favorable and an unfavorable group seems to be justified to allow for a more individualized therapy in a quite heterogenous group of patients. So far, multiple randomized trials have shown a benefit when radiation therapy (RT) is combined with ADT. The use of dose-escalated RT without ADT also appears to be an adequate therapy associated with a very low rate of cancer-specific deaths. Therefore, taking into account the increased rate of toxicity associated with ADT, dose-escalated RT alone might be justified, especially in favorable intermediate-risk patients.

CONCLUSION

Dose-escalated RT alone appears to be an appropriate treatment in favorable intermediate-risk patients. Addition of short course ADT (4-6 months) might improve outcomes in unfavorable intermediate-risk patients.

摘要

目的

本文旨在概述联合放射治疗和雄激素剥夺治疗(ADT)在中危前列腺癌患者中的作用。

材料和方法

回顾了目前德国、欧洲和 NCCN(美国国家综合癌症网络)指南以及 PubMed 数据库中关于中危组亚分类和 ADT 在肿瘤学结果方面应用的相关文献。

结果

目前有不同的局部前列腺癌患者风险组评估建议。将中危分为有利和不利亚组似乎是合理的,以便为一组相当异质的患者提供更个体化的治疗。到目前为止,多项随机试验表明,放射治疗(RT)联合 ADT 具有获益。不联合 ADT 进行剂量递增 RT 似乎也是一种有效的治疗方法,癌症特异性死亡的发生率非常低。因此,考虑到 ADT 相关毒性增加的发生率,单独进行剂量递增 RT 可能是合理的,特别是在有利的中危患者中。

结论

单独进行剂量递增 RT 似乎是有利中危患者的合适治疗方法。在不利的中危患者中,添加短期 ADT(4-6 个月)可能会改善预后。

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本文引用的文献

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Effect of Standard vs Dose-Escalated Radiation Therapy for Patients With Intermediate-Risk Prostate Cancer: The NRG Oncology RTOG 0126 Randomized Clinical Trial.标准剂量与剂量递增放疗治疗中危前列腺癌患者的效果:NRG 肿瘤学 RTOG 0126 随机临床试验。
JAMA Oncol. 2018 Jun 14;4(6):e180039. doi: 10.1001/jamaoncol.2018.0039.
2
Use of androgen deprivation and salvage radiation therapy for patients with prostate cancer and biochemical recurrence after prostatectomy.雄激素剥夺治疗联合挽救性放疗用于前列腺癌根治术后生化复发患者。
Strahlenther Onkol. 2018 Jul;194(7):619-626. doi: 10.1007/s00066-018-1269-3. Epub 2018 Jan 30.
3
2005 年至 2015 年期间德国局限性高危前列腺癌男性患者中激素治疗的不充分应用:基于登记数据的分析。
BMC Cancer. 2022 Jun 7;22(1):624. doi: 10.1186/s12885-022-09677-z.
4
Ultrahypofractionation of localized prostate cancer : Statement from the DEGRO working group prostate cancer.局限性前列腺癌的超分割治疗:来自 DEGRO 工作组前列腺癌声明。
Strahlenther Onkol. 2021 Feb;197(2):89-96. doi: 10.1007/s00066-020-01723-8. Epub 2020 Dec 10.
5
Treatment strategies to prevent and reduce gynecomastia and/or breast pain caused by antiandrogen therapy for prostate cancer : Statement from the DEGRO working group prostate cancer.用于预防和减少前列腺癌抗雄激素治疗所致男性乳房发育症和/或乳房疼痛的治疗策略:DEGRO 工作组前列腺癌声明。
Strahlenther Onkol. 2020 Jul;196(7):589-597. doi: 10.1007/s00066-020-01598-9. Epub 2020 Mar 12.
Androgen-deprivation therapy, dementia, and cognitive dysfunction in men with prostate cancer: How much smoke and how much fire?
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Cancer. 2018 Apr 1;124(7):1326-1334. doi: 10.1002/cncr.31153. Epub 2018 Jan 16.
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J Clin Oncol. 2018 Feb 20;36(6):581-590. doi: 10.1200/JCO.2017.74.2940. Epub 2017 Nov 29.
5
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8
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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.
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JAMA Oncol. 2017 Jan 1;3(1):49-55. doi: 10.1001/jamaoncol.2016.3662.