Fuchs Bruno, Schelling Georg, Glanzmann Christoph, Studer Gabriela
Faculty of Health Sciences & Medicine, University Lucerne, Frohburgstrasse 3, 6002 Luzern, Switzerland.
Sarcoma Service, Department of Orthopedics and Trauma, Sarcoma Center, LUKS University Hospital, 6000 Luzern, Switzerland.
Cancers (Basel). 2025 May 21;17(10):1724. doi: 10.3390/cancers17101724.
The SU2C-SARC032 randomized controlled trial (RCT) tested pembrolizumab combined with preoperative normofractionated radiotherapy as an intensified treatment for high-risk stage III resectable soft tissue sarcoma (STS), demonstrating a moderate improvement in disease-free survival (DFS) compared to preoperative radiotherapy alone, but accompanied by significantly increased toxicity, prolonged treatment durations, elevated resource source, and limited real-world applicability. To address the gap between highly controlled trial outcomes and routine clinical practice, this comparative analysis evaluated a streamlined ultra-hypofractionated preoperative radiotherapy (uhpRT) protocol using real-world data (RWD) as a potentially more balanced approach. Prospectively collected observational RWD from 54 consecutive patients with Stage III (T2 N0 M0) high-risk resectable STS treated at a single institution with uhpRT (25 Gy in 5 fractions in one week, no systemic therapy, median interval of 14 days to surgery) were analyzed. Survival endpoints (overall survival [OS], DFS, local disease-free survival [LDFS], distant disease-free survival [DDFS]), toxicity, and treatment duration were compared qualitatively with published outcomes from the SU2C-SARC032 trial's intensified pembrolizumab arm and control arm. At 2 years, the optimized uhpRT protocol achieved OS (90%), DFS (66%), and DDFS (70%) comparable to the intensified pembrolizumab arm (OS: 88%, DFS: 67%, DDFS (67%)) and clearly exceeded outcomes of the control arm (OS/DFS/DDFS: 85%/52%/52%). Importantly, the uhpRT protocol markedly reduced treatment-related toxicities (0% Grade 3/4 events vs. 56% in the intensified trial arm) and total treatment duration (<1 month vs. 3-11 months). These findings challenge the necessity of broad treatment intensification for high-risk localized STS, strongly supporting the concept of therapeutic optimization. Given substantial real-world variability in treatment practices and feasibility highlighted by recent research, our findings advocate for treatment strategies that prioritize realistic applicability, patient safety, and value-based care principles over pure intensification.
SU2C-SARC032随机对照试验(RCT)对帕博利珠单抗联合术前常规分割放疗作为高危III期可切除软组织肉瘤(STS)的强化治疗进行了测试,结果表明,与单纯术前放疗相比,无病生存期(DFS)有适度改善,但同时毒性显著增加、治疗时间延长、资源消耗增加且实际应用受限。为了弥合高度对照试验结果与常规临床实践之间的差距,本比较分析使用真实世界数据(RWD)评估了一种简化的超分割术前放疗(uhpRT)方案,作为一种可能更平衡的方法。对在单一机构接受uhpRT(一周内分5次给予25 Gy,不进行全身治疗,手术中位间隔时间为14天)的54例连续III期(T2 N0 M0)高危可切除STS患者前瞻性收集的观察性RWD进行了分析。将生存终点(总生存期[OS]、DFS、局部无病生存期[LDFS]、远处无病生存期[DDFS])、毒性和治疗持续时间与SU2C-SARC032试验强化帕博利珠单抗组和对照组已发表的结果进行了定性比较。在2年时,优化后的uhpRT方案实现的OS(90%)、DFS(66%)和DDFS(70%)与强化帕博利珠单抗组相当(OS:88%,DFS:67%,DDFS:67%),且明显超过对照组的结果(OS/DFS/DDFS:85%/52%/52%)。重要的是,uhpRT方案显著降低了治疗相关毒性(3/4级事件为0%,而强化试验组为56%)和总治疗持续时间(<1个月对3 - 11个月)。这些发现对高危局限性STS广泛强化治疗的必要性提出了挑战,有力地支持了治疗优化的概念。鉴于近期研究强调的治疗实践和可行性在现实世界中的巨大差异,我们的发现倡导优先考虑现实适用性、患者安全和基于价值的医疗原则而非单纯强化的治疗策略。