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前列腺癌根治术后挽救性放疗的前列腺特异性抗原反应与无进展生存期和总生存期相关。

The PSA-response to salvage radiotherapy after radical prostatectomy correlates with freedom from progression and overall survival.

作者信息

Bartkowiak Detlef, Bottke Dirk, Thamm Reinhard, Siegmann Alessandra, Hinkelbein Wolfgang, Wiegel Thomas

机构信息

University Hospital Ulm, Department of Radiation Oncology, Ulm, Germany.

Charité University Hospital, Department of Radiation Oncology, Berlin, Germany.

出版信息

Radiother Oncol. 2016 Jan;118(1):131-5. doi: 10.1016/j.radonc.2015.10.028. Epub 2015 Nov 30.

Abstract

BACKGROUND AND PURPOSE

In a retrospective analysis, we examined factors influencing the outcome of prostate cancer (PCa) patients receiving salvage radiotherapy (SRT) for PSA recurrence after radical prostatectomy (RP).

MATERIAL AND METHODS

306 patients received 3D-conformal SRT at a median pre-SRT PSA of 0.298 ng/ml. Post-SRT progression was defined as PSA ⩾0.2 ng/ml above nadir and rising further, or hormone treatment, or clinical recurrence. Data were analyzed with the Kaplan-Meier method and multivariable Cox regression.

RESULTS

Application of SRT at a PSA <0.2 ng/ml correlated significantly with achieving a post-SRT PSA nadir <0.1 ng/ml and with improved freedom from progression (median follow-up 7.2 years). The post-SRT nadir <0.1 ng/ml correlated significantly with less recurrences and with better overall survival. In multivariable Cox analysis restricted to pre-SRT parameters, a pre-SRT PSA ⩾0.2 ng/ml had the strongest impact (hazard ratio 2.4) on progression. If the post-SRT PSA nadir was included in the model, then failing the nadir was the most important risk factor (hazard ratio 8.1).

CONCLUSIONS

Early SRT at a PSA <0.2 ng/ml is a favorable treatment option for post-RP biochemical recurrence. It correlated with a post-SRT PSA-nadir <0.1 ng/ml which was associated with improved freedom from progression and overall survival.

摘要

背景与目的

在一项回顾性分析中,我们研究了影响前列腺癌(PCa)患者在根治性前列腺切除术(RP)后接受挽救性放疗(SRT)治疗PSA复发的因素。

材料与方法

306例患者接受了三维适形SRT,SRT前中位PSA为0.298 ng/ml。SRT后进展定义为PSA比最低点升高≥0.2 ng/ml且持续上升,或接受激素治疗,或临床复发。采用Kaplan-Meier法和多变量Cox回归分析数据。

结果

PSA<0.2 ng/ml时应用SRT与SRT后PSA最低点<0.1 ng/ml以及更好的无进展生存期显著相关(中位随访7.2年)。SRT后最低点<0.1 ng/ml与较少的复发和更好的总生存期显著相关。在仅限于SRT前参数的多变量Cox分析中,SRT前PSA≥0.2 ng/ml对进展的影响最大(风险比2.4)。如果将SRT后PSA最低点纳入模型,那么未达到最低点是最重要的风险因素(风险比8.1)。

结论

PSA<0.2 ng/ml时早期进行SRT是RP后生化复发的一种有利治疗选择。它与SRT后PSA最低点<0.1 ng/ml相关,而这又与更好的无进展生存期和总生存期相关。

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