Division of Oncology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Comprehensive Cancer Center Graz, Medical University of Graz, Graz, Austria.
Ann Surg Oncol. 2018 Mar;25(3):776-783. doi: 10.1245/s10434-017-6080-3. Epub 2017 Sep 11.
This study aimed to quantify the benefit of adjuvant radiotherapy (AXRT) for local control, distant metastasis, and long-term survival outcomes in patients with localized soft tissue sarcoma (STS).
This single-center retrospective observational study enrolled 433 STS patients who underwent surgery with curative intent. An inverse probability of treatment-weighted (IPTW) analysis was implemented to account rigorously for imbalances in prognostic variables between the adjuvant treatment groups.
During a median follow-up period of 5.5 years, the study observed 38 local recurrences (9%), 73 occurrences of distant metastasis (17%), 63 STS-related deaths (15%), and 57 deaths from other causes (13%). As expected, patients receiving AXRT (n = 258, 60%) were more likely to have high-grade G3 tumors (p < 0.0001) than patients not receiving AXRT. A crude analysis showed that AXRT was not associated with improved recurrence-free survival [hazard ratio (HR) 1.00; 95% confidence interval (CI) 0.72-1.38; p = 0.98]. However, after IPTW, AXRT was associated with a 38% relative reduction in the risk of recurrence or death (HR 0.62; 95% CI 0.39-1.00; p = 0.05). This benefit was driven by a strong reduction in the risk of local recurrence (HR 0.42; 95% CI 0.19-0.91; p = 0.03), whereas the relative risk of distant metastasis (HR 0.69; 95% CI 0.39-1.25; p = 0.22) and overall survival (HR 0.76; 95% CI 0.44-1.30; p = 0.32) were only nonsignificantly in favor of AXRT. An exploratory analysis showed an overall survival benefit of AXRT for patients with high-grade G3 tumors (HR 0.51; 95% CI 0.33-0.78; p = 0.002). However, this finding may have been attributable to residual confounding.
In this observational cohort, AXRT was associated with a 58% reduction in the relative risk of local recurrence. No consistent association between AXRT and lower risks of distant metastasis or death was observed.
本研究旨在量化辅助放疗(AXRT)对局限性软组织肉瘤(STS)患者局部控制、远处转移和长期生存结局的获益。
本单中心回顾性观察性研究纳入了 433 名接受根治性手术治疗的 STS 患者。采用逆概率治疗加权(IPTW)分析严格校正辅助治疗组之间预后变量的不平衡。
在中位随访 5.5 年期间,研究观察到 38 例局部复发(9%)、73 例远处转移(17%)、63 例 STS 相关死亡(15%)和 57 例其他原因死亡(13%)。正如预期的那样,接受 AXRT(n=258,60%)的患者更有可能患有高级别 G3 肿瘤(p<0.0001)。粗分析显示,AXRT 与无复发生存率的改善无关[风险比(HR)1.00;95%置信区间(CI)0.72-1.38;p=0.98]。然而,经过 IPTW 后,AXRT 与复发或死亡风险降低 38%相关(HR 0.62;95%CI 0.39-1.00;p=0.05)。这种获益主要归因于局部复发风险的显著降低(HR 0.42;95%CI 0.19-0.91;p=0.03),而远处转移(HR 0.69;95%CI 0.39-1.25;p=0.22)和总生存(HR 0.76;95%CI 0.44-1.30;p=0.32)的相对风险仅无统计学意义地有利于 AXRT。一项探索性分析显示,高级别 G3 肿瘤患者的 AXRT 具有总生存获益(HR 0.51;95%CI 0.33-0.78;p=0.002)。然而,这一发现可能归因于残留混杂。
在这项观察性队列研究中,AXRT 与局部复发的相对风险降低 58%相关。AXRT 与远处转移或死亡风险降低之间没有一致的关联。