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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。

Use of androgen deprivation and salvage radiation therapy for patients with prostate cancer and biochemical recurrence after prostatectomy.

机构信息

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

Inselspital, University of Bern, Bern, Switzerland.

出版信息

Strahlenther Onkol. 2018 Jul;194(7):619-626. doi: 10.1007/s00066-018-1269-3. Epub 2018 Jan 30.

Abstract

AIM

Overview on the use of androgen deprivation therapy (ADT) added to salvage radiation therapy (SRT) for prostate cancer patients with biochemical recurrence after prostatectomy.

METHODS

The German Society of Radiation Oncology (DEGRO) expert panel summarized available evidence published between January 2009 and May 2017, and assessed the validity of the information on outcome parameters including overall survival (OS) and treatment-related toxicity.

RESULTS

Two randomized controlled trials and nine relevant retrospective analyses were identified. The RTOG 9601 trial showed an OS improvement for the combination of 2 years of bicalutamide and SRT compared to SRT alone after a median follow-up of 13 years. This improvement appeared to be restricted to those patients with a prostate specific antigen (PSA) level before SRT of ≥0.7 ng/mL. The GETUG AFU-16 trial showed that after a median follow-up of 5 years, the addition of 6 months of goserelin to SRT improved progression-free survival (PFS; based on biochemical recurrence) as compared to SRT alone. ADT in both trials was not associated with increased major late toxicities. Results of retrospective series were inconsistent with a suggestion that the addition of ADT improved biochemical PFS especially in patients with high-risk factors such as Gleason Score ≥8 and in the group with initially negative surgical margins.

CONCLUSIONS

ADT combined with SRT appears to improve OS in patients with a PSA level before SRT of ≥0.7 ng/mL. In patients without persistent PSA after prostatectomy and PSA levels of <0.7 ng/mL, ADT should not routinely be used, but may be considered in patients with additional risk factors such as Gleason Score ≥8 and negative surgical margins.

摘要

目的

概述去势治疗(ADT)联合挽救性放疗(SRT)在前列腺癌根治术后生化复发患者中的应用。

方法

德国放射肿瘤学会(DEGRO)专家组总结了 2009 年 1 月至 2017 年 5 月期间发表的现有证据,并评估了总生存(OS)和治疗相关毒性等结局参数的信息有效性。

结果

共确定了两项随机对照试验和九项相关的回顾性分析。RTOG 9601 试验表明,与单独 SRT 相比,在中位随访 13 年后,2 年比卡鲁胺联合 SRT 可改善 OS。这种改善似乎仅限于 SRT 前 PSA 水平≥0.7ng/mL 的患者。GETUG AFU-16 试验表明,在中位随访 5 年后,与单独 SRT 相比,SRT 联合 6 个月戈舍瑞林可改善无进展生存(PFS;基于生化复发)。两项试验中的 ADT 均未导致严重晚期毒性增加。回顾性系列研究的结果不一致,提示 ADT 联合治疗可改善生化 PFS,尤其是在具有高风险因素(如 Gleason 评分≥8 和最初切缘阴性)的患者中。

结论

ADT 联合 SRT 似乎可改善 SRT 前 PSA 水平≥0.7ng/mL 的患者的 OS。对于前列腺根治术后 PSA 持续阴性且 PSA<0.7ng/mL 的患者,不应常规使用 ADT,但对于具有其他危险因素(如 Gleason 评分≥8 和切缘阴性)的患者,可考虑使用 ADT。

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