Division of Thoracic Surgery, McGill University Health Centre, Montréal, Quebec, Canada.
Department of Thoracic and Cardiovascular Surgery, The University of Texas MD Anderson Cancer Center, Houston, Texas; Department of Epidemiology, Human Genetics and Environmental Sciences, The University of Texas Health Science Center (UTHealth) School of Public Health, Houston, Texas.
Ann Thorac Surg. 2019 Jan;107(1):277-284. doi: 10.1016/j.athoracsur.2018.07.033. Epub 2018 Sep 15.
Induction chemoradiation for resectable N2 non-small cell lung cancer (NSCLC) is used with the intent to optimize locoregional control, whereas induction chemotherapy given in systemic doses is meant to optimally target potential distant disease. However, the optimal preoperative treatment regimen is still unknown and practice patterns continue to vary widely. We compared multiinstitutional oncologic outcomes for N2 NSCLC from 4 experienced lung cancer treatment centers.
This collaborative retrospective study unites 4 major thoracic oncology centers. Patients with N2 NSCLC undergoing surgical resection after induction chemotherapy (CxT) or concurrent chemoradiation (CxRT) were included. Primary outcomes were overall and disease-free survival (OS and DFS).
822 patients were identified (CxT = 662 and CxRT = 160). There were no differences in 5-year OS (CxT 39.9% versus CxRT 42.9%, p = 0.250) nor in DFS (CxT 28.7% versus 29.8%, p = 0.207). Recurrence rates (CxT 46.8% versus CxRT 51.6%, p = 0.282) and recurrence patterns were not significantly different (Local: CxT 9.8% versus CxRT 9.7%; and Distant: CxT 30.4% versus CxRT 33.1%, p = 0.764). There was no difference in perioperative mortality. In the analyses of patients who underwent pretreatment invasive mediastinal staging (n = 555), there were still no significant differences in OS (p = 0.341) and DFS (p = 0.455) between the 2 treatment strategies.
Both treatment strategies produce equivalent and better than expected outcomes compared with historical controls for N2 NSCLC, with no differences in recurrence patterns. How these conventional therapeutic strategies will compare with those involving immunotherapy combined with surgical locoregional disease control for N2 disease remains to be determined.
可切除 N2 非小细胞肺癌(NSCLC)采用诱导放化疗旨在优化局部区域控制,而全身剂量给予诱导化疗旨在最佳靶向潜在远处疾病。然而,最佳术前治疗方案仍不清楚,且实践模式仍存在很大差异。我们比较了 4 个经验丰富的肺癌治疗中心的 N2 NSCLC 的多机构肿瘤学结果。
这项合作回顾性研究联合了 4 个主要的胸科肿瘤中心。纳入接受诱导化疗(CxT)或同步放化疗(CxRT)后行手术切除的 N2 NSCLC 患者。主要结局是总生存(OS)和无病生存(DFS)。
共纳入 822 例患者(CxT 662 例,CxRT 160 例)。5 年 OS 无差异(CxT 39.9% vs CxRT 42.9%,p=0.250),DFS 也无差异(CxT 28.7% vs CxRT 29.8%,p=0.207)。复发率(CxT 46.8% vs CxRT 51.6%,p=0.282)和复发模式无显著差异(局部:CxT 9.8% vs CxRT 9.7%;远处:CxT 30.4% vs CxRT 33.1%,p=0.764)。围手术期死亡率无差异。在对行术前侵袭性纵隔分期的患者(n=555)进行分析时,2 种治疗策略在 OS(p=0.341)和 DFS(p=0.455)方面仍无显著差异。
与 N2 NSCLC 的历史对照相比,这两种治疗策略都产生了等效甚至更好的结果,且复发模式无差异。这些传统治疗策略与将免疫治疗与手术局部区域疾病控制相结合用于 N2 疾病的策略相比如何,还有待确定。