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

被引:0
作者
Ghadjar, Pirus [1 ]
Aebersold, Daniel M. [2 ]
Albrecht, Clemens [3 ]
Boehmer, Dirk [1 ]
Flentje, Michael [4 ]
Ganswindt, Ute [5 ]
Hoecht, Stefan [6 ]
Hoelscher, Tobias [7 ]
Sedlmayer, Felix [8 ]
Wenz, Frederik [9 ]
Zips, Daniel [10 ]
Wiegel, Thomas [11 ]
机构
[1] Charite Univ Med Berlin, Dept Radiat Oncol, Augustenburger Pl 1, D-13353 Berlin, Germany
[2] Univ Bern, Inselspital, Bern, Switzerland
[3] Klinikum Nurnberg Nord, Nurnberg, Germany
[4] Univ Klinikum Wurzburg, Wurzburg, Germany
[5] Ludwig Maximilians Univ Munchen, Munich, Germany
[6] Xcare Grp, Radiol Nukl Med & Strahlentherapie, Saarlouis, Germany
[7] Tech Univ Dresden, Univ Klinikum Carl Gustav Carus, Dresden, Germany
[8] Paracelsus Med Privatuniv, Landeskrankenhaus, Univ Klinikum, Salzburg, Austria
[9] Heidelberg Univ, Univ Med Mannheim, Mannheim, Germany
[10] Univ Klinikum Tubingen, Tubingen, Germany
[11] Univ Klinikum Ulm, Ulm, Germany
关键词
Prostate cancer; Radical prostatectomy; Salvage radiation therapy; Androgen deprivation therapy; Hormone therapy; RADICAL PROSTATECTOMY; RISING PSA; RADIOTHERAPY; ANTIGEN; OUTCOMES; SURVIVAL; TRIAL; MEN; METAANALYSIS; SUPPRESSION;
D O I
10.1007/s00066-018-1269-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Overview on the use of androgen deprivation therapy (ADT) added to salvage radiation therapy (SRT) for prostate cancer patients with biochemical recurrence after prostatectomy. 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. 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.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. ADT combined with SRT appears to improve OS in patients with a PSA level before SRT of >= 0.7ng/mL. In patients without persistent PSA after prostatectomy and PSA levels of < 0.7ng/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.
引用
收藏
页码:619 / 626
页数:8
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