Böhmer Dirk, Siegmann Alessandra, Scharl Sophia, Ruf Christian, Wiegel Thomas, Krafcsik Manuel, Thamm Reinhard
Department of Radiation Oncology, Charité University Medicine, Campus Benjamin Franklin, 12203 Berlin, Germany.
Department of Radiation Oncology, University Hospital Ulm, 89081 Ulm, Germany.
Cancers (Basel). 2022 Mar 4;14(5):1320. doi: 10.3390/cancers14051320.
Previous randomized trials have not provided conclusive evidence about dose escalations and associated toxicities for salvage radiotherapy (SRT) in prostate cancer. Here, we retrospectively analyzed whether dose escalations influenced progression-free survival in 554 patients that received salvage radiotherapy for relapses or persistently elevated prostate cancer antigen (PSA) after a radical prostatectomy. Patients received SRT between 1997 and 2017 at two University Hospitals in Germany. We compared patient groups that received radiation doses <7000 cGy (n = 225) or ≥7000 cGy (n = 329) to analyze the influence of radiation dose on progression-free survival. In a second matched-pair analysis of 216 pairs, we evaluated prognostic factors (pT2 vs. pT3−4, Gleason score [GS] ≤ 7 vs. GS ≥ 8, R0 vs. R1, and pre-SRT PSA <0.5 vs. ≥0.5 ng/mL). After a median follow-up of 6.8 (4.2−9.2) years, we found that escalated doses significantly improved progression-free survival (p = 0.0042). A multivariate analysis indicated that an escalated dose, lower tumor stages (pT2 vs. pT3/4), and lower GSs (≤7 vs. 8−10) were associated with improved progression-free survival. There was no significant effect on overall survival. Our data suggested that escalating the radiation dose to ≥7000 cGy for SRT after a prostatectomy significantly improved progression-free survival. Longer follow-ups are needed for a comprehensive recommendation.
既往的随机试验尚未提供关于前列腺癌挽救性放疗(SRT)剂量递增及相关毒性的确凿证据。在此,我们回顾性分析了剂量递增对554例前列腺癌根治术后复发或前列腺癌抗原(PSA)持续升高而接受挽救性放疗患者无进展生存期的影响。1997年至2017年期间,德国两家大学医院的患者接受了SRT。我们比较了接受辐射剂量<7000 cGy(n = 225)或≥7000 cGy(n = 329)的患者组,以分析辐射剂量对无进展生存期的影响。在对216对患者的第二项配对分析中,我们评估了预后因素(pT2与pT3−4、 Gleason评分[GS]≤7与GS≥8、R0与R1以及SRT前PSA<0.5与≥0.5 ng/mL)。中位随访6.8(4.2−9.2)年后,我们发现剂量递增显著改善了无进展生存期(p = 0.0042)。多因素分析表明,剂量递增、较低的肿瘤分期(pT2与pT3/4)以及较低的GSs(≤7与8−10)与改善的无进展生存期相关。对总生存期无显著影响。我们的数据表明,前列腺切除术后SRT将辐射剂量增至≥7000 cGy可显著改善无进展生存期。需要更长时间的随访以给出全面的建议。