Will Baseline Total Lesion Glycolysis Play a Role in Improving the Prognostic Value of the NCCN-IPI in Primary Gastric Diffuse Large B-Cell Lymphoma Patients Treated With the R-CHOP Regimen?

医学 国际预后指标 弥漫性大B细胞淋巴瘤 内科学 养生 肿瘤科 癌症 阶段(地层学) 回顾性队列研究 淋巴瘤 胃肠病学 生物 古生物学
作者
Chong Jiang,Chongyang Ding,Jingyan Xu,Yue Teng,Jieyu Chen,Zhen Wang,Zhengyang Zhou,Chong Jiang,Yue Teng,Zhengyang Zhou
出处
期刊:Clinical Nuclear Medicine [Ovid Technologies (Wolters Kluwer)]
卷期号:46 (1): 1-7 被引量:7
标识
DOI:10.1097/rlu.0000000000003378
摘要

Purpose The aim was to explore whether baseline total lesion glycolysis (TLG) can improve the prognostic value of the National Comprehensive Cancer Network International Prognostic Index (NCCN-IPI) in primary gastric diffuse large B-cell lymphoma (PG-DLBCL) patients treated with an R-CHOP–like regimen. Materials and Methods Ninety-four PG-DLBCL patients who underwent baseline PET/CT between July 2010 and May 2019 were included in this retrospective study. FDG-avid lesions in each patient were segmented to calculate the SUV max , total metabolic tumor volume (TMTV), and TLG. Progression-free survival (PFS) and overall survival (OS) were used as end points to evaluate prognosis. Results During the follow-up period of 5 to 108 months (35.3 ± 23.5 months), high TLG and a high NCCN-IPI were significantly associated with poor PFS and OS. Total lesion glycolysis and the NCCN-IPI were independent predictors of PFS and OS. Patients were stratified into 3 groups according to the combination of TLG and the NCCN-IPI for PFS ( P < 0.001) and OS ( P < 0.001): high-risk group (TLG > 1159.1 and NCCN-IPI 4–8) (PFS and OS, 57.7% and 61.5%, respectively, n = 42), intermediate-risk group (TLG > 1159.1 or NCCN-IPI 4–8) (PFS and OS, both 76.9%, n = 26), and low-risk group (TLG ≤ 1159.1 and NCCN-IPI 0–3) (PFS and OS, 97.6% and 100.0%, respectively, n = 26). Conclusions Both TLG and the NCCN-IPI are independent predictors of PG-DLBCL patient survival. Moreover, the combination of TLG and the NCCN-IPI improved patient risk stratification and might help personalize therapeutic regimens.
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