Radiotherapy after radical prostatectomy: immediate or early delayed?

Background Biochemical recurrence after radical prostatectomy (RP) is associated with risk indicators, including Gleason score, preoperative PSA level, tumor stage, seminal vesicle invasion, and positive surgical margins. The 5-year biochemical progression rate among predisposed patients is as high...

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Veröffentlicht in:Strahlentherapie und Onkologie 2012-12, Vol.188 (12), p.1096-1101
Hauptverfasser: Bottke, D., Bartkowiak, D., Schrader, M., Wiegel, T.
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creator Bottke, D.
Bartkowiak, D.
Schrader, M.
Wiegel, T.
description Background Biochemical recurrence after radical prostatectomy (RP) is associated with risk indicators, including Gleason score, preoperative PSA level, tumor stage, seminal vesicle invasion, and positive surgical margins. The 5-year biochemical progression rate among predisposed patients is as high as 50–70%. Post-RP treatment options include adjuvant radiotherapy (ART, for men with undetectable PSA) or salvage radiotherapy (SRT, for PSA persisting or re-rising above detection threshold). Presently, there are no published randomized trials evaluating ART vs. SRT directly. Methods Published data on ART and SRT were reviewed to allow a comparison of the two treatment approaches. Results Three randomized phase III trials demonstrated an almost 20% absolute benefit for biochemical progression-free survival after ART (60–64 Gy) compared to a “wait and see” policy. The greatest benefit was achieved in patients with positive margins and pT3 tumors. SRT can be offered to patients with elevated PSA after RP. In 30–70% of SRT patients, PSA will decrease to an undetectable level, thus giving a second curative chance. The rate of side effects for both treatments is comparably low. The role of irradiation of pelvic lymph nodes and the additional use of hormone therapy and radiation dose are discussed. Conclusion It remains unclear whether early SRT initiated after PSA failure is equivalent to ART. Where SRT is indicated, it should be started as early as possible.
doi_str_mv 10.1007/s00066-012-0234-9
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The 5-year biochemical progression rate among predisposed patients is as high as 50–70%. Post-RP treatment options include adjuvant radiotherapy (ART, for men with undetectable PSA) or salvage radiotherapy (SRT, for PSA persisting or re-rising above detection threshold). Presently, there are no published randomized trials evaluating ART vs. SRT directly. Methods Published data on ART and SRT were reviewed to allow a comparison of the two treatment approaches. Results Three randomized phase III trials demonstrated an almost 20% absolute benefit for biochemical progression-free survival after ART (60–64 Gy) compared to a “wait and see” policy. The greatest benefit was achieved in patients with positive margins and pT3 tumors. SRT can be offered to patients with elevated PSA after RP. In 30–70% of SRT patients, PSA will decrease to an undetectable level, thus giving a second curative chance. The rate of side effects for both treatments is comparably low. The role of irradiation of pelvic lymph nodes and the additional use of hormone therapy and radiation dose are discussed. Conclusion It remains unclear whether early SRT initiated after PSA failure is equivalent to ART. 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The 5-year biochemical progression rate among predisposed patients is as high as 50–70%. Post-RP treatment options include adjuvant radiotherapy (ART, for men with undetectable PSA) or salvage radiotherapy (SRT, for PSA persisting or re-rising above detection threshold). Presently, there are no published randomized trials evaluating ART vs. SRT directly. Methods Published data on ART and SRT were reviewed to allow a comparison of the two treatment approaches. Results Three randomized phase III trials demonstrated an almost 20% absolute benefit for biochemical progression-free survival after ART (60–64 Gy) compared to a “wait and see” policy. The greatest benefit was achieved in patients with positive margins and pT3 tumors. SRT can be offered to patients with elevated PSA after RP. In 30–70% of SRT patients, PSA will decrease to an undetectable level, thus giving a second curative chance. The rate of side effects for both treatments is comparably low. The role of irradiation of pelvic lymph nodes and the additional use of hormone therapy and radiation dose are discussed. Conclusion It remains unclear whether early SRT initiated after PSA failure is equivalent to ART. 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The 5-year biochemical progression rate among predisposed patients is as high as 50–70%. Post-RP treatment options include adjuvant radiotherapy (ART, for men with undetectable PSA) or salvage radiotherapy (SRT, for PSA persisting or re-rising above detection threshold). Presently, there are no published randomized trials evaluating ART vs. SRT directly. Methods Published data on ART and SRT were reviewed to allow a comparison of the two treatment approaches. Results Three randomized phase III trials demonstrated an almost 20% absolute benefit for biochemical progression-free survival after ART (60–64 Gy) compared to a “wait and see” policy. The greatest benefit was achieved in patients with positive margins and pT3 tumors. SRT can be offered to patients with elevated PSA after RP. In 30–70% of SRT patients, PSA will decrease to an undetectable level, thus giving a second curative chance. The rate of side effects for both treatments is comparably low. The role of irradiation of pelvic lymph nodes and the additional use of hormone therapy and radiation dose are discussed. Conclusion It remains unclear whether early SRT initiated after PSA failure is equivalent to ART. Where SRT is indicated, it should be started as early as possible.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer-Verlag</pub><pmid>23128897</pmid><doi>10.1007/s00066-012-0234-9</doi><tpages>6</tpages></addata></record>
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subjects Biomarkers, Tumor - blood
Combined Modality Therapy
Disease-Free Survival
Follow-Up Studies
Guideline Adherence
Humans
Lymphatic Irradiation
Magnetic Resonance Imaging
Male
Medicine
Medicine & Public Health
Neoplasm Grading
Neoplasm Recurrence, Local - pathology
Neoplasm Recurrence, Local - radiotherapy
Neoplasm Recurrence, Local - surgery
Neoplasm Staging
Neoplasm, Residual - pathology
Neoplasm, Residual - radiotherapy
Neoplasm, Residual - surgery
Oncology
Original Article
Prostate-Specific Antigen - blood
Prostatectomy
Prostatic Neoplasms - mortality
Prostatic Neoplasms - pathology
Prostatic Neoplasms - radiotherapy
Prostatic Neoplasms - surgery
Radiotherapy
Radiotherapy Dosage
Radiotherapy Planning, Computer-Assisted
Radiotherapy, Adjuvant - methods
Randomized Controlled Trials as Topic
Salvage Therapy - methods
Time-to-Treatment
title Radiotherapy after radical prostatectomy: immediate or early delayed?
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