Hashimoto Kosuke, Kaira Kyoichi, Imai Hisao, Mouri Atsuto, Shiono Ayako, Miura Yu, Yamaguchi Ou, Kobayashi Kunihiko, Kagamu Hiroshi, Kuji Ichiei
Departments of Respiratory Medicine.
Nuclear Medicine, International Medical Center, Saitama Medical University, Hidaka City, Saitama, Japan.
J Immunother. 2022 Oct 1;45(8):349-357. doi: 10.1097/CJI.0000000000000434. Epub 2022 Aug 19.
Combined chemotherapy plus programmed death-1 (PD-1) blockade is an established treatment against patients with advanced non-small cell lung cancer (NSCLC). However, a promising predictor besides programmed death ligand-1 expression remains uncertain. We examined the prognostic significance of baseline 18 F-FDG-positron emission tomography for predicting first-line combined chemotherapy plus PD-1 blockade in NSCLC patients. Forty-five patients with advanced NSCLC who received 18 F-FDG-positron emission tomography immediately before combined platinum-based chemotherapy with PD-1 blockade as first-line setting were eligible for this study, and assessment of maximum of standard uptake value (SUV max ), metabolic tumor volume (MTV), and total lesion glycolysis (TLG) on 18 F-FDG uptake was performed. The objective response rate, median progression-free survival, and overall survival were 51.2%, 206 days, and 681 days, respectively. High SUV max , TLG, and MTV significantly correlated with age and performance status (PS), C-reactive protein (CRP), and PS, CRP, albumin, and baseline tumor size, respectively. Univariate analysis identified albumin, TLG and MTV as significant predictors of progression-free survival, and CRP, albumin, TLG and MTV as significant factors for predicting overall survival. High TLG was confirmed as an independent factor associated with poor prognosis in multivariate analysis. In particular, TLG is identified as the most powerful predictor in patients with good PS, adenocarcinoma, programmed death ligand-1≥1%, and low baseline tumor size. The tumor metabolic volume by MTV and TLG at pretreatment was clarified as a significant predictor for combined chemotherapy with PD-1 blockade, but not maximal glycolytic level by SUV max .
联合化疗加程序性死亡受体1(PD-1)阻断是晚期非小细胞肺癌(NSCLC)患者的既定治疗方法。然而,除了程序性死亡配体1表达外,一种有前景的预测指标仍不明确。我们研究了基线18F-FDG正电子发射断层扫描对NSCLC患者一线联合化疗加PD-1阻断的预后意义。45例晚期NSCLC患者在接受以铂类为基础的联合化疗加PD-1阻断作为一线治疗前立即接受了18F-FDG正电子发射断层扫描,符合本研究条件,并对18F-FDG摄取的最大标准摄取值(SUVmax)、代谢肿瘤体积(MTV)和总病灶糖酵解(TLG)进行了评估。客观缓解率、中位无进展生存期和总生存期分别为51.2%、206天和681天。高SUVmax、TLG和MTV分别与年龄和体能状态(PS)、C反应蛋白(CRP)以及PS、CRP、白蛋白和基线肿瘤大小显著相关。单因素分析确定白蛋白、TLG和MTV是无进展生存期的重要预测指标,CRP、白蛋白、TLG和MTV是总生存期的重要预测因素。多因素分析证实高TLG是与预后不良相关的独立因素。特别是,TLG被确定为PS良好、腺癌、程序性死亡配体1≥1%且基线肿瘤大小低的患者中最有力的预测指标。预处理时MTV和TLG所反映的肿瘤代谢体积被明确为联合化疗加PD-1阻断的重要预测指标,但SUVmax所反映的最大糖酵解水平不是。