Department of Radiation Oncology, Jewish General Hospital, McGill University, Montreal, QC H3T 1E2, Canada.
Department of Clinical Oncology, Tanta University Hospitals, Tanta University, Tanta 6632110, Egypt.
Curr Oncol. 2023 Aug 1;30(8):7252-7262. doi: 10.3390/curroncol30080526.
To report the long-term outcomes of the McGill 0913 study and the potential benefits of combining prostate-bed radiotherapy (PBRT), pelvic-lymph-node radiotherapy (PLNRT), and long term ADT (LT-ADT).
From 2010 to 2016, 46 high-risk prostate cancer patients who experienced biochemical recurrence (BCR) after radical prostatectomy (RP) were enrolled in this single-arm phase II clinical trial. The patients were eligible if they had a Gleason score > 8, locally advanced disease (≥pT3), a preoperative PSA of >20 ng/mL, or positive lymph nodes (LN). The patients were treated with a combination of 24 months of ADT, PBRT, and PLNRT. The primary outcome was biochemical progression-free survival (bPFS) and the predefined secondary endpoints included distant-metastasis-free survival (DMFS), overall survival (OS), and toxicity. In this update, we also report the median follow-up of 8.8 years and 10 years OS.
At a median follow-up of 8.8 years, 43 patients were eligible for analysis. The median pre-salvage PSA was 0.30 μg/L. Half (51%) of the patients ( = 22) had positive margins, 40% ( = 17) had Gleason scores > 8, 63% ( = 27) had extracapsular extension, 42% ( = 18) had seminal vesicle invasion, and 19% ( = 8) had LN involvement. The 10-year bPFS was 68.3 %. The 10-year DMFS was 72.9%. The 10-year OS was 97%. There were two non-cancer-related deaths. The first patient died of congestive heart failure while the other died of an unknown cause. No new toxicity was observed after the initial report.
Our study demonstrates that treatment escalation with PBRT, PLNRT, and LT-ADT improves long term outcomes. In view of the recently published SPPORT study, we conclude that this novel approach of treatment intensification in high-risk post-prostatectomy patients is safe and effective, and that it should be offered as the standard of care.
报告 McGill0913 研究的长期结果,以及联合前列腺床放疗(PBRT)、盆腔淋巴结放疗(PLNRT)和长期 ADT(LT-ADT)的潜在益处。
2010 年至 2016 年,46 例接受根治性前列腺切除术(RP)后出现生化复发(BCR)的高危前列腺癌患者入组本单臂 II 期临床试验。符合条件的患者包括 Gleason 评分>8、局部晚期疾病(≥pT3)、术前 PSA>20ng/mL 或阳性淋巴结(LN)。患者接受 24 个月 ADT、PBRT 和 PLNRT 联合治疗。主要结局是生化无进展生存期(bPFS),预设的次要结局包括远处无转移生存期(DMFS)、总生存期(OS)和毒性。在本次更新中,我们还报告了中位随访 8.8 年和 10 年 OS。
中位随访 8.8 年后,43 例患者符合分析条件。挽救性治疗前 PSA 的中位数为 0.30μg/L。一半(51%)的患者(=22)有阳性切缘,40%(=17)的 Gleason 评分>8,63%(=27)有包膜外延伸,42%(=18)有精囊侵犯,19%(=8)有淋巴结受累。10 年 bPFS 为 68.3%。10 年 DMFS 为 72.9%。10 年 OS 为 97%。有 2 例非癌症相关死亡。第一例患者死于充血性心力衰竭,另一例患者死因不明。初始报告后未观察到新的毒性。
我们的研究表明,联合 PBRT、PLNRT 和 LT-ADT 的治疗升级可改善长期结局。鉴于最近发表的 SPORT 研究,我们得出结论,这种在高危前列腺癌术后患者中强化治疗的新方法是安全有效的,应作为标准治疗方法提供。