Prostate-specific antigen after salvage radiotherapy for postprostatectomy biochemical recurrence predicts long-term outcome including overall survival

Authors

  • Detlef Bartkowiak Department of Radiation Oncology, University Hospital Ulm, Germany
  • Reinhard Thamm Department of Radiation Oncology, University Hospital Ulm, Germany
  • Dirk Bottke Department of Radiation Oncology, Esslingen Hospital, Germany
  • Alessandra Siegmann Department of Radiation Oncology, Charité University Hospital Berlin, Germany
  • Dirk Böhmer Department of Radiation Oncology, Charité University Hospital Berlin, Germany
  • Volker Budach Department of Radiation Oncology, Charité University Hospital Berlin, Germany
  • Thomas Wiegel Department of Radiation Oncology, University Hospital Ulm, Germany

DOI:

https://doi.org/10.1080/0284186X.2017.1364869

Abstract

Background: For patients with recurrent prostate cancer after radical prostatectomy (RP), salvage radiotherapy (SRT) is a second chance of cure. However, depending on risk factors, 40–70% of the patients experience further progression. With a focus on the pre- and post-SRT serum level of the prostate-specific antigen (PSA), we assessed the determinants of the long-term outcome after SRT.

Patient and methods: Between 1997 and 2011, 464 patients received 3D-conformal SRT with median 66.6 Gy. The median PSA level before SRT was 0.31 ng/ml. In our retrospective analysis, post-SRT progression was defined as either a rising PSA >0.2 ng/ml above the nadir, or the application of anti-androgens or clinical recurrence. A PSA <0.1 ng/ml was termed undetectable. We analyzed the data with the Kaplan–Meier method (Logrank test) and multivariable Cox regression.

Results: The median follow-up was 5.9 years. Overall, 178 patients had recurrence, 13 developed distant metastases and 30 died. Univariate, a pre-RP PSA <10 ng/ml, pathological stage pT <3, Gleason score <8, positive surgical margins, a pre-SRT PSA <0.2 ng/ml and a post-SRT PSA nadir <0.1 ng/ml correlated with fewer and later second recurrences. In a multivariable Cox model, pT, Gleason score, margin status and pre-SRT PSA were significant covariates of progression. If the post-SRT PSA response was included in the regression analysis, then a nadir ≥0.1 ng/ml was the strongest risk factor. Initiating SRT at a PSA <0.2 ng/ml correlated with a post-SRT PSA <0.1 ng/ml. Men who achieved an undetectable post-SRT PSA nadir also had lower rates of metastases and a better overall survival. However, there were too few events for Cox regression analysis of these two endpoints.

Conclusions: Early SRT at a PSA <0.2 ng/ml correlates with re-achieving an undetectable PSA, which predicts improved freedom from progression and metastases and better overall survival.

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Published

2018-03-04

How to Cite

Bartkowiak, D., Thamm, R., Bottke, D., Siegmann, A., Böhmer, D., Budach, V., & Wiegel, T. (2018). Prostate-specific antigen after salvage radiotherapy for postprostatectomy biochemical recurrence predicts long-term outcome including overall survival. Acta Oncologica, 57(3), 362–367. https://doi.org/10.1080/0284186X.2017.1364869