2-[18F]FDG PET/CT预处理肿瘤负荷和播散特征在晚期套细胞淋巴瘤中的预后作用

IF 3.3 4区 医学 Q2 HEMATOLOGY Hematological Oncology Pub Date : 2024-11-29 DOI:10.1002/hon.70009
Domenico Albano, Nicola Bianchetti, Anna Talin, Francesco Dondi, Alessandro Re, Alessandra Tucci, Francesco Bertagna
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引用次数: 0

摘要

套细胞淋巴瘤(MCL)是一种侵袭性非霍奇金淋巴瘤,预后不良。氟-18-氟脱氧葡萄糖正电子发射断层扫描/计算机断层扫描(2-[18F]FDG PET/CT)及其参数在评估治疗反应和预后中的作用尚不清楚。本研究的目的是探讨肿瘤负荷和2-[18F]FDG PET/CT得出的肿瘤播散特征在晚期MCL中的预后作用。我们回顾性地纳入了120例晚期MCL患者,他们接受了基线2- 2-[18F]FDG PET/CT和治疗末期(eot) PET/CT检查。通过测量最大标准化摄取值体重(SUVbw)、瘦体重(SUVlbm)、体表面积(SUVbsa)、代谢肿瘤体积(MTV)、病变总糖酵解(TLG)和播散特征(Dmax和Dmax-bsa),对基线- pet图像进行视觉和半定量分析。EotPET/CT按照Lugano分类进行判断。根据Kaplan-Meier法绘制无进展生存期(PFS)和总生存期(OS)。在中位随访59个月时,68例患者复发/进展,38例患者死亡,中位PFS和OS分别为27.2个月和57.6个月。单因素分析显示,MIPI评分、笨重疾病、Ki-67指数、代谢反应、预处理MTV和TLG与PFS显著相关,但仅代谢反应、MTV和TLG被证实为独立的预后因素。考虑到OS,只有传播特征被证明是预后特征。综上所述,代谢反应和代谢性肿瘤负荷参数(MTV和TLG)是PFS的最强预测因子,而播散特征可能对OS有重要的预测作用。
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Prognostic Role of Pretreatment Tumor Burden and Dissemination Features From 2-[18F]FDG PET/CT in Advanced Mantle Cell Lymphoma

Mantle cell lymphoma (MCL) is an aggressive non-Hodgkin lymphoma with poor prognosis. The usefulness of fluorine-18-fluorodeoxyglucose positron emission tomography/computed tomography (2-[18F]FDG PET/CT) and its parameters in the evaluation of treatment response and prognosis is not yet clear. The aim of this study was to investigate the prognostic role of tumor burden and tumor dissemination features derived by 2-[18F]FDG PET/CT in advanced MCL. We retrospectively included 120 patients with advanced MCL who underwent baseline 2- 2-[18F]FDG PET/CT and end-of-treatment (eot) PET/CT. The baseline-PET images were analyzed visually and semi-quantitatively by measuring the maximum standardized uptake value body weight (SUVbw), lean body mass (SUVlbm), body surface area (SUVbsa), metabolic tumor volume (MTV), total lesion glycolysis (TLG) and dissemination features (Dmax and Dmax-bsa). EotPET/CT was judged according to the Lugano classification. Progression-free survival (PFS) and overall survival (OS) were plotted according to the Kaplan–Meier method. At a median follow-up of 59 months, relapse/progression occurred in 68 patients while death in 38 patients with a median PFS and OS of 27.2 and 57.6 months, respectively. MIPI score, Bulky disease, Ki-67 index, metabolic response, pretreatment MTV and TLG were significantly associated with PFS at univariate analysis, but only metabolic response, MTV and TLG were confirmed to be independent prognostic factors. Considering OS, only dissemination features were demonstrated to be prognostic features. In conclusions, metabolic response and metabolic tumor burden parameters (MTV and TLG) are strongest predictor of PFS, while dissemination features may have a significant role for predicting OS.

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来源期刊
Hematological Oncology
Hematological Oncology 医学-血液学
CiteScore
4.20
自引率
6.10%
发文量
147
审稿时长
>12 weeks
期刊介绍: Hematological Oncology considers for publication articles dealing with experimental and clinical aspects of neoplastic diseases of the hemopoietic and lymphoid systems and relevant related matters. Translational studies applying basic science to clinical issues are particularly welcomed. Manuscripts dealing with the following areas are encouraged: -Clinical practice and management of hematological neoplasia, including: acute and chronic leukemias, malignant lymphomas, myeloproliferative disorders -Diagnostic investigations, including imaging and laboratory assays -Epidemiology, pathology and pathobiology of hematological neoplasia of hematological diseases -Therapeutic issues including Phase 1, 2 or 3 trials as well as allogeneic and autologous stem cell transplantation studies -Aspects of the cell biology, molecular biology, molecular genetics and cytogenetics of normal or diseased hematopoeisis and lymphopoiesis, including stem cells and cytokines and other regulatory systems. Concise, topical review material is welcomed, especially if it makes new concepts and ideas accessible to a wider community. Proposals for review material may be discussed with the Editor-in-Chief. Collections of case material and case reports will be considered only if they have broader scientific or clinical relevance.
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