[18F]FDG Metabolic Tumor Volume as a Prognostic Marker in Neuroendocrine Neoplasm: A Multicenter Study

David L. Chan, Aimee Hayes, Ioannis Karfis, Alice Conner, Magdalena Mileva, Elizabeth Bernard, Shaunak Navalkissoor, Gopinath Gnanasekaran, Stephen J. Clarke, Paul J. Roach, Patrick Flamen, Martyn E. Caplin, Nick Pavlakis, Christos Toumpanakis, Dale L. Bailey
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Abstract

[18F]FDG PET/CT avidity predicts higher-grade disease and worse prognosis in patients with metastatic neuroendocrine neoplasm. However, there is less evidence regarding the role of [18F]FDG-avid tumor volume in predicting prognosis. We planned to determine whether metabolic tumor volume (MTV) on [18F]FDG PET/CT predicts prognosis in patients with advanced gastroenteropancreatic neuroendocrine neoplasm (GEPNEN). Methods: A multicenter retrospective study was performed on patients with advanced GEPNEN who underwent [18F]FDG PET/CT in a previously established cohort. Images were acquired across 3 centers using harmonized protocols and were contoured and verified at a flat SUV threshold of 4 using a semiautomated software workflow. The primary endpoint was overall survival. Patients were dichotomized into high- and low-MTV groups by the median value, with the overall survival of the 2 resulting cohorts compared by log-rank tests and multivariate analyses. Results: In total, 231 patients were included (49% male; median age, 60 y). In 45% of cases the primary was the pancreas, in 42% the small bowel, and in 13% another location. Regarding World Health Organization 2019 grade, 23% were grade 1, 52% grade 2, 21% grade 3, and 4% an unknown grade. The median follow-up was 27 mo (interquartile range, 11–49 mo), and median overall survival was 38.6 mo. Median overall survival was shorter in the high-MTV cohort than in the low-MTV cohort (cut point, 16.5 cm3; 23.8 mo vs. not reached; hazard ratio, 2.49; 95% CI, 1.69–3.66; P < 0.0001). Median time to treatment failure was also shorter in the high-MTV cohort (11.7 mo vs. 16.9 mo; hazard ratio, 1.52; 95% CI, 1.13–2.06; P = 0.005). Increasing histologic grade was associated with higher MTV (P = 0.0006, 1-way ANOVA). Multivariate analysis incorporating age, grade, sex, SUVmax, and MTV showed that only grade (P = 0.001) and MTV (P < 0.001) were independently prognostic. Conclusion: MTV is a prognostic biomarker in advanced GEPNEN. Reports of [18F]FDG PET in GEPNEN may benefit from comments on MTV in addition to the degree of [18F]FDG avidity.

[18]FDG代谢肿瘤体积与神经内分泌肿瘤预后的相关性研究
[18F]FDG PET/CT贪婪度预测转移性神经内分泌肿瘤的高级别病变和较差预后。然而,关于[18F]FDG-avid肿瘤体积在预测预后中的作用的证据较少。我们计划确定[18F]FDG PET/CT上的代谢肿瘤体积(MTV)是否能预测晚期胃肠胰神经内分泌肿瘤(GEPNEN)患者的预后。方法:对先前建立的队列中接受[18F]FDG PET/CT检查的晚期GEPNEN患者进行多中心回顾性研究。使用统一的协议在3个中心获取图像,并使用半自动软件工作流在平坦的SUV阈值4下进行轮廓和验证。主要终点是总生存期。根据中位数将患者分为高mtv组和低mtv组,并通过对数秩检验和多变量分析比较两组患者的总生存期。结果:共纳入231例患者(49%男性;中位年龄60岁)。在45%的病例中,原发灶在胰腺,42%在小肠,13%在其他部位。关于世界卫生组织2019年的分级,23%为1级,52%为2级,21%为3级,4%为未知级别。中位随访时间为27个月(四分位间距为11-49个月),中位总生存期为38.6个月。高mtv组的中位总生存期短于低mtv组(切点为16.5 cm3;23.8月vs.未达到;风险比2.49;95% ci, 1.69-3.66;P & lt;0.0001)。在高mtv组中,治疗失败的中位时间也更短(11.7个月vs 16.9个月;风险比1.52;95% ci, 1.13-2.06;P = 0.005)。组织学分级越高,MTV越高(P = 0.0006,单因素方差分析)。纳入年龄、年级、性别、SUVmax和MTV的多变量分析显示,只有年级(P = 0.001)和MTV (P <;0.001)独立预测预后。结论:MTV是晚期GEPNEN的预后生物标志物。关于GEPNEN中[18F]FDG PET的报道,除了[18F]FDG的贪婪程度外,还可以从MTV上的评论中获益。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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