Huang Mingxing, Zou Yuheng, Wang Weichen, Li Qianrui, Tian Rong
Department of Nuclear Medicine, West China Hospital, Sichuan University, Chengdu, China.
Department of Nuclear Medicine, West China Hospital, Sichuan University, 37 Guoxue Alley, Chengdu, Sichuan 610041, China.
Ther Adv Med Oncol. 2024 Nov 4;16:17588359241293364. doi: 10.1177/17588359241293364. eCollection 2024.
The value of pretreatment baseline F-fluorodeoxyglucose positron emission tomography (F-FDG PET)/computed tomography (CT) as a prognostic factor for survival of patients with non-small-cell lung cancer (NSCLC) receiving immunotherapy remained uncertain.
To investigate the prognostic ability of baseline F-FDG PET/CT in patients with NSCLC receiving immunotherapy.
A systematic review and meta-analysis.
We searched the PubMed, EMBASE, and Cochrane Central Register of Controlled Trials databases until May 7, 2024, and extracted data related to patient characteristics, semiquantitative parameters of F-FDG PET/CT, and survival. We pooled hazard ratios (HRs) to evaluate the prognostic value of the maximum standardized uptake value (SUV), mean standardized uptake value (SUV), metabolic tumor volume (MTV), and total lesion glycolysis (TLG) for overall survival (OS) and progression-free survival (PFS).
A total of 22 studies (1363 patients, average age range 30-88 years) were included. Baseline F-FDG PET/CT-derived MTV was significantly associated with both OS (HR: 1.124, 95% confidence interval (CI) 1.058-1.195, = 81.70%) and PFS (HR: 1.069, 95% CI: 1.016-1.124, = 71.80%). Other baseline F-FDG PET/CT-derived parameters, including SUV (OS: HR: 0.930, 95% CI: 0.718-1.230; PFS: HR: 0.979, 95% CI: 0.759-1.262), SUV (OS: HR: 0.801, 95% CI: 0.549-1.170; PFS: HR: 0.688, 95% CI: 0.464-1.020), and TLG (OS: HR: 0.999, 95% CI: 0.980-1.018; PFS: HR: 0.995, 95% CI: 0.980-1.010), were not associated with survival. Sensitivity analyses by removing one study at a time did not significantly alter the association between MTV and PFS or between MTV and OS. There was no evidence of publication bias.
Pretreatment baseline F-FDG PET/CT-derived MTV might be a prognostic biomarker in NSCLC patients receiving immunotherapy. Further studies are needed to support routine use.
对于接受免疫治疗的非小细胞肺癌(NSCLC)患者,治疗前基线氟脱氧葡萄糖正电子发射断层扫描(F-FDG PET)/计算机断层扫描(CT)作为生存预后因素的价值仍不确定。
探讨基线F-FDG PET/CT对接受免疫治疗的NSCLC患者的预后评估能力。
系统评价和荟萃分析。
检索截至2024年5月7日的PubMed、EMBASE和Cochrane对照试验中央注册库数据库,并提取与患者特征、F-FDG PET/CT的半定量参数及生存相关的数据。汇总风险比(HR)以评估最大标准化摄取值(SUV)、平均标准化摄取值(SUV)、代谢肿瘤体积(MTV)和总病灶糖酵解(TLG)对总生存期(OS)和无进展生存期(PFS)的预后价值。
共纳入22项研究(1363例患者,平均年龄范围30 - 88岁)。基线F-FDG PET/CT衍生的MTV与OS(HR:1.124,95%置信区间(CI)1.058 - 1.195,P = 81.70%)和PFS(HR:1.069,95% CI:1.016 - 1.124,P = 71.80%)均显著相关。其他基线F-FDG PET/CT衍生参数,包括SUV(OS:HR:0.930,95% CI:0.718 - 1.230;PFS:HR:0.979,95% CI:0.759 - 1.262)、SUV(OS:HR:0.8立,95% CI:0.549 - 1.170;PFS:HR:0.688,95% CI:0.464 - 1.020)和TLG(OS:HR:0.999,95% CI:0.980 - 1.018;PFS:HR:0.995,95% CI:0.980 - 1.010)与生存均无关联。每次剔除一项研究进行的敏感性分析未显著改变MTV与PFS或MTV与OS之间的关联。没有证据表明存在发表偏倚。
治疗前基线F-FDG PET/CT衍生的MTV可能是接受免疫治疗的NSCLC患者的预后生物标志物。需要进一步研究以支持其常规应用。