Torso FDG-PET parameters as prognostic biomarkers for advanced non-small cell lung cancer patients undergoing first-line immunotherapy and chemotherapy

躯干FDG-PET参数作为接受一线免疫治疗和化疗的晚期非小细胞肺癌患者的预后生物标志物

阅读:1

Abstract

BACKGROUND: The objective of this study was to investigate the prognostic significance of parameters derived from ¹⁸F-fluorodeoxyglucose (FDG) positron emission tomography (PET) imaging in patients with advanced non-small cell lung cancer (NSCLC) receiving first-line treatment with immune checkpoint inhibitors (ICIs) and platinum-based chemotherapy, focusing on both primary tumors and metastatic sites located in the torso. METHODS: This retrospective study analyzed 70 patients diagnosed with stage III or IV NSCLC who underwent FDG PET/computed tomography (CT) prior to initiating first-line treatment with ICI-based combination therapy. Key metabolic metrics-including maximum standardized uptake value (SUVmax), metabolic tumor volume (MTV), and total lesion glycolysis (TLG)-were quantified across all detectable lesions within the torso. Associations between these PET-derived parameters and clinical outcomes, including progression-free survival (PFS) and overall survival (OS), were examined using Kaplan-Meier survival estimates and Cox proportional hazards regression. RESULTS: MTV-torso and TLG-torso were significantly higher in patients with poor Eastern Cooperative Oncology Group performance status (PS ≥ 2). In univariate analyses, PS, MTV-torso, and TLG-torso were significantly associated with both PFS and OS. In multivariate analyses, PS and MTV-torso remained independent predictors of both outcomes. Patients with lower MTV-torso (< 225.81) had significantly higher mean PFS (582.3 vs. 154.5 days, P < 0.001) and OS (1,047.6 vs. 291.4 days, P < 0.001). SUVmax-torso was not significantly associated with survival. CONCLUSIONS: Among the FDG PET-based volumetric indices, MTV-torso emerged as an independent predictor of both PFS and OS in patients with advanced NSCLC undergoing first-line treatment with ICI and platinum-based chemotherapy. These findings support the use of torso-based metabolic tumor burden assessment as a valuable tool for prognostic stratification in this patient population.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。