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基线 18FDG-PET/CT 扫描中的代谢异质性是原发性纵隔 B 细胞淋巴瘤患者预后的预测因素。

Metabolic heterogeneity on baseline 18FDG-PET/CT scan is a predictor of outcome in primary mediastinal B-cell lymphoma.

机构信息

Nuclear Medicine and PET/CT Centre, Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.

Department of Cellular Biotechnologies and Hematology, Sapienza University, Rome, Italy.

出版信息

Blood. 2018 Jul 12;132(2):179-186. doi: 10.1182/blood-2018-01-826958. Epub 2018 May 2.

Abstract

An important unmet need in the management of primary mediastinal B-cell lymphoma (PMBCL) is to identify the patients for whom first-line therapy will fail to intervene before the lymphoma becomes refractory. High heterogeneity of intratumoral F-fluorodeoxyglucose (18FDG) uptake distribution on positron emission tomography/computed tomography (PET/CT) scans has been suggested as a possible marker of chemoresistance in solid tumors. In the present study, we investigated the prognostic value of metabolic heterogeneity (MH) in 103 patients with PMBCL prospectively enrolled in the International Extranodal Lymphoma Study Group (IELSG) 26 study, aimed at clarifying the role of PET in this lymphoma subtype. MH was estimated using the area under curve of cumulative standardized uptake value-volume histogram (AUC-CSH) method. Progression-free survival at 5 years was 94% vs 73% in low- and high-MH groups, respectively ( = .0001). In a Cox model of progression-free survival including dichotomized MH, metabolic tumor volume, total lesion glycolysis (TLG), international prognostic index, and tumor bulk (mediastinal mass > 10 cm), as well as age as a continuous variable, only TLG ( < .001) and MH ( < .001) retained statistical significance. Using these 2 features to construct a simple prognostic model resulted in early and accurate (positive predictive value, 89%; negative predictive value, ≥90%) identification of patients at high risk for progression at a point that would allow the use of risk-adapted treatments. This may provide an important opportunity for the design of future trials aimed at helping the minority of patients who harbor chemorefractory PMBCL. The study is registered at ClinicalTrials.gov as NCT00944567.

摘要

原发性纵隔 B 细胞淋巴瘤(PMBCL)治疗中一个重要的未满足需求是在淋巴瘤发生耐药之前,确定一线治疗将失败的患者。正电子发射断层扫描/计算机断层扫描(PET/CT)扫描上肿瘤内 F-氟脱氧葡萄糖(18FDG)摄取分布的高度异质性已被认为是实体瘤中化学耐药的可能标志物。在本研究中,我们前瞻性地研究了 103 例 PMBCL 患者的代谢异质性(MH)的预后价值,这些患者前瞻性地纳入了国际结外淋巴瘤研究组(IELSG)26 研究,旨在阐明 PET 在这种淋巴瘤亚型中的作用。MH 使用累积标准化摄取值-容积直方图的曲线下面积(AUC-CSH)方法进行评估。低 MH 组和高 MH 组的 5 年无进展生存率分别为 94%和 73%(=.0001)。在包括 MH 二分类、代谢肿瘤体积、总病变糖酵解(TLG)、国际预后指数和肿瘤体积(纵隔肿块>10cm)以及年龄作为连续变量的无进展生存 Cox 模型中,只有 TLG( <.001)和 MH( <.001)保留了统计学意义。使用这两个特征构建一个简单的预后模型,可以早期、准确地(阳性预测值,89%;阴性预测值,≥90%)识别出进展风险高的患者,这将允许使用风险适应治疗。这可能为旨在帮助少数存在化疗耐药 PMBCL 的患者的未来试验设计提供一个重要机会。该研究在 ClinicalTrials.gov 上注册为 NCT00944567。

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