18F-FDG PET/CT 和 CECT 的纹理分析:预测纵隔大块受累的霍奇金淋巴瘤的难治性。

IF 3.3 4区 医学 Q2 HEMATOLOGY
Elisabetta M. Abenavoli, Flavia Linguanti, Matilde Anichini, Vittorio Miele, Francesco Mungai, Marianna Palazzo, Luca Nassi, Benedetta Puccini, Ilaria Romano, Benedetta Sordi, Roberto Sciagrà, Gabriele Simontacchi, Alessandro M. Vannucchi, Valentina Berti
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引用次数: 0

摘要

为识别难治性疾病高风险患者,仍需确定新的预后参数,以改善新诊断霍奇金淋巴瘤(HL)的分层。本研究探讨了从基线 18F-FDG 正电子发射/计算机断层扫描(PET)和对比增强计算机断层扫描(CECT)中提取的代谢和纹理特征与临床数据相结合,在预测纵隔大块受累的典型 HL(cHL)一线治疗难治性(R)方面的潜在价值。我们回顾了 69 例接受 PET 和 CECT 分期检查的 cHL 患者。我们使用免费软件 LIFEx 6.3 进行了病灶分割和纹理参数提取。评估了临床和影像学特征对难治性疾病发展的预后意义。通过接收者操作特征曲线、Cox比例危险回归和Kaplan-Meier分析来研究潜在的独立预测因素并评估其预后价值。在临床特征中,只有根据德国霍奇金小组(GHSG)分类系统划分的分期在R和非R之间存在显著差异。在CECT变量中,只有从二阶矩阵(灰度级共现矩阵(GLCM)和灰度级运行长度矩阵(GLRLM))得出的参数具有明显的预后能力。在 PET 变量中,SUVmean、从一阶分析(直方图、形状)和二阶分析(GLCM、GLRLM、NGLDM)得出的几个变量显示出显著的预测能力。在接收者操作特征分析中,这些变量的准确率超过 70%,其 PFS 曲线在预测难治性方面具有统计学意义。在多变量分析中,只有从 PET 中提取的 HISTO_EntropyPET (HISTO_EntropyPET)和 GHSG 分期是显著的独立预测因子。它们的组合确定了 4 个患者组,其 PFS 曲线明显不同,无论分期如何,HISTO_EntropyPET 值越高的患者预后越差。影像放射组学可为纵隔膨出型 cHL 患者的预后评估提供参考。将HISTO_EntropyPET与GHSG分期相结合,对预测R型与非R型疾病具有最佳预后价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Texture analysis of 18F-FDG PET/CT and CECT: Prediction of refractoriness of Hodgkin lymphoma with mediastinal bulk involvement

To recognize patients at high risk of refractory disease, the identification of novel prognostic parameters improving stratification of newly diagnosed Hodgkin Lymphoma (HL) is still needed. This study investigates the potential value of metabolic and texture features, extracted from baseline 18F-FDG Positron Emission Tomography/Computed Tomography (PET) and Contrast-Enhanced Computed Tomography scan (CECT), together with clinical data, in predicting first-line therapy refractoriness (R) of classical HL (cHL) with mediastinal bulk involvement. We reviewed 69 cHL patients who underwent staging PET and CECT. Lesion segmentation and texture parameter extraction were performed using the freeware software LIFEx 6.3. The prognostic significance of clinical and imaging features was evaluated in relation to the development of refractory disease. Receiver operating characteristic curve, Cox proportional hazard regression and Kaplan-Meier analyses were performed to examine the potential independent predictors and to evaluate their prognostic value. Among clinical characteristics, only stage according to the German Hodgkin Group (GHSG) classification system significantly differed between R and not-R. Among CECT variables, only parameters derived from second order matrices (gray-level co-occurrence matrix (GLCM) and gray-level run length matrix (GLRLM) demonstrated significant prognostic power. Among PET variables, SUVmean, several variables derived from first (histograms, shape), and second order analyses (GLCM, GLRLM, NGLDM) exhibited significant predictive power. Such variables obtained accuracies greater than 70% at receiver operating characteristic analysis and their PFS curves resulted statistically significant in predicting refractoriness. At multivariate analysis, only HISTO_EntropyPET extracted from PET (HISTO_EntropyPET) and GHSG stage resulted as significant independent predictors. Their combination identified 4 patient groups with significantly different PFS curves, with worst prognosis in patients with higher HISTO_EntropyPET values, regardless of the stage. Imaging radiomics may provide a reference for prognostic evaluation of patients with mediastinal bulky cHL. The best prognostic value in the prediction of R versus not-R disease was reached by combining HISTO_EntropyPET with GHSG stage.

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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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