Ribeirão Preto Medical School, Department of Medical Imagings, Hematology and Oncology of University of São Paulo (FMRP-USP), Ribeirão Preto, Brazil; Latin America Cooperative Oncology Group (LACOG), Porto Alegre, Brazil.
Latin America Cooperative Oncology Group (LACOG), Porto Alegre, Brazil; Department of Oncology - Division of Radiation Oncology, Juravinski Cancer Centre, McMaster University, Hamilton, ON, Canada.
Radiother Oncol. 2024 Dec;201:110439. doi: 10.1016/j.radonc.2024.110439. Epub 2024 Jul 19.
To evaluate the feasibility, efficacy and safety of stereotactic ablative radiotherapy (SABR) to the primary tumor and lymph nodes in patients with locally advanced non-small cell lung cancer (LA-NSCLC) who are ineligible for or refused concomitant chemoradiation.
In accordance with the PRISMA and MOOSE guidelines, a systematic review with meta-analysis was conducted. The study included reports that assessed the outcomes of SABR treatment in patients with LA-NSCLC. Studies evaluating SBRT as a boost following primary radiotherapy were excluded. The primary outcomes measured were local control (LC) and overall survival (OS). The secondary endpoint was the incidence of severe toxicity (grades 3-5). A meta-regression analysis was performed to explore the relationship between LC, OS, and severe toxicity. The Biologically Effective Dose (BED) was analyzed as a continuous variable. Statistical significance was defined as a p-value < 0.05.
A total of seven studies (3 prospective and 4 retrospective studies) involving 268 patients (SBRT to primary and lymph nodes) were included in the analysis. The pooled 1-year LC rate was 80 % (95 % CI: 63-94 %), and the factors significantly associated with LC were BEDGy10 (p = 0.005) and neoadjuvant chemotherapy (p = 0.005). The 1-year and 2-year OS rates were 74 % (95 % CI: 58-90 %) and 55 % (95 % CI: 34-76 %), respectively. Meta-regression analysis indicated a linear relationship between OS and LC, with a 0.7 % increase in OS for each 1 % improvement in LC (p = 0.005). The pooled rate of grade 3 acute toxicity was 5 % (95 % CI: 1-10 %), and the rate of grade 5 toxicity was 1.7 % (95 % CI: 0-3 %).
Promising results (LC and OS) with limited toxicity (feasibility) using SABR in LA-NSCLC warrant further research, emphasizing the need for larger, well-designed trials for further validation of the approach.
评估立体定向消融放疗(SABR)在不适合或拒绝同期放化疗的局部晚期非小细胞肺癌(LA-NSCLC)患者原发肿瘤和淋巴结中的可行性、疗效和安全性。
根据 PRISMA 和 MOOSE 指南,进行了系统评价和荟萃分析。该研究包括评估 SABR 治疗 LA-NSCLC 患者结局的报告。排除了评估 SBRT 作为原发性放疗后增敏的研究。主要结局测量是局部控制(LC)和总生存(OS)。次要终点是严重毒性(3-5 级)的发生率。进行了荟萃回归分析以探讨 LC、OS 和严重毒性之间的关系。生物有效剂量(BED)被分析为连续变量。统计显著性定义为 p 值 < 0.05。
共纳入了 7 项研究(3 项前瞻性和 4 项回顾性研究),共 268 例患者(原发肿瘤和淋巴结的 SBRT)纳入分析。1 年 LC 率的汇总率为 80%(95%CI:63-94%),与 LC 显著相关的因素是 BEDGy10(p=0.005)和新辅助化疗(p=0.005)。1 年和 2 年 OS 率分别为 74%(95%CI:58-90%)和 55%(95%CI:34-76%)。荟萃回归分析表明 OS 与 LC 之间存在线性关系,LC 每提高 1%,OS 提高 0.7%(p=0.005)。3 级急性毒性的汇总发生率为 5%(95%CI:1-10%),5 级毒性的发生率为 1.7%(95%CI:0-3%)。
SABR 在 LA-NSCLC 中具有有希望的结果(LC 和 OS)和有限的毒性(可行性),值得进一步研究,强调需要更大、设计良好的试验进一步验证该方法。