Baron D, Pasquier D, Pace-Loscos T, Vandendorpe B, Schiappa R, Ortholan C, Hannoun-Levi J M
Department of Radiotherapy, Centre Antoine Lacassagne, University Cote d'Azur, Nice, France.
Department of Radiotherapy Centre Oscar Lambret, Lille, France.
Clin Transl Radiat Oncol. 2023 Aug 31;43:100673. doi: 10.1016/j.ctro.2023.100673. eCollection 2023 Nov.
To evaluate the oncological outcome after stereotactic body radiation therapy (SBRT) for oligometastatic hormone-sensitive prostate cancer (omHSPC) patients.
MATERIALS-METHODS: In this retrospective, observational, multi-institutional study, omHSPC patients (≤5 metastases) underwent SBRT. Primary endpoint was systemic therapy escalation-free survival (STE-FS) after SBRT. Local (LR), distant (DR), prostatic (PR) and isolated biochemical (iBR) relapses were reported with progression-free survival (PFS) and overall survival (OS). Prognostic factors for STE-FS were investigated. Toxicity was reported.
From 01/07 to 09/19, 119 pts with omHSPC underwent SBRT. With a MFU of 34 months [12-97], median STE-FS was 33.4 months (95%CI 26.6---40.1). Median OS was not reached and PFS was 22.7 months (CI95% 18.6---32.3). Post-SBRT-PSA remained stable or decreased in 87 pts (73.1%). Progression events (LR, MR, PR, iBR) were observed in 72 pts (60.5%), among whom 6 relapsed in the irradiated area (local control rate: 95%). DR, BR, PR were observed in 44 pts (37%), 21pts (17.7%) and 2 pts (1.7%) respectively. In multivariate analysis, post-SBRT biochemical response was an independent prognostic factor for STE-FS. Grade ≥ 3 toxicity occurred in 1pt.
With excellent local control and tolerance, SBRT for omHSPC patients represents an attractive approach to defer systemic therapeutic escalation and prevent its side effects. Accurate patient selection for SBRT requires more data with longer follow-up and higher numbers of patients pending the results of upcoming randomized trials.
评估寡转移激素敏感性前列腺癌(omHSPC)患者接受立体定向体部放射治疗(SBRT)后的肿瘤学结局。
在这项回顾性、观察性、多机构研究中,omHSPC患者(转移灶≤5个)接受了SBRT。主要终点是SBRT后的无全身治疗升级生存期(STE-FS)。报告了局部(LR)、远处(DR)、前列腺(PR)和孤立生化(iBR)复发情况以及无进展生存期(PFS)和总生存期(OS)。研究了STE-FS的预后因素。报告了毒性情况。
2007年1月至2019年9月,119例omHSPC患者接受了SBRT。中位随访时间为34个月[12 - 97个月],中位STE-FS为33.4个月(95%CI 26.6 - 40.1)。总生存期未达到中位值,PFS为22.7个月(95%CI 18.6 - 32.3)。87例患者(73.1%)SBRT后的前列腺特异性抗原(PSA)保持稳定或下降。72例患者(60.5%)出现进展事件(LR、MR、PR、iBR),其中6例在放疗区域复发(局部控制率:95%)。分别在44例患者(37%)、21例患者(17.7%)和2例患者(1.7%)中观察到DR、BR、PR。多因素分析显示,SBRT后的生化反应是STE-FS的独立预后因素。1例患者发生≥3级毒性反应。
SBRT对omHSPC患者具有良好的局部控制和耐受性,是一种有吸引力的延缓全身治疗升级并预防其副作用的方法。准确选择适合SBRT的患者需要更多数据,进行更长时间的随访以及纳入更多患者,以待即将开展的随机试验结果。