Hunutlu Fazıl Çağrı, Öztop Hikmet, Gürsoy Vildan, Ersal Tuba, Elgün Ezel, Yavuz Şeyma, İldemir Ekizoğlu Selin, Ekizoğlu Azim Ali, Özkocaman Vildan, Özkalemkaş Fahir
Division of Hematology, Department of Internal Medicine, Faculty of Medicine, Bursa Uludag University, Bursa 16059, Turkey.
Department of Internal Medicine, Faculty of Medicine, Bursa Uludag University, Bursa 16059, Turkey.
Diagnostics (Basel). 2025 Jan 14;15(2):185. doi: 10.3390/diagnostics15020185.
Although the cure rates of classical Hodgkin Lymphoma (cHL) are as high as 90% using the current treatment protocols, the prognosis is poor for primary refractory patients. Thus, a biomarker that can predict patients with early progression at the time of diagnosis is an unmet clinical need. Endothelial activation and stress index (EASIX) and its variant modified EASIX (mEASIX) is a scoring system currently used for the prediction of prognosis in hematologic malignancies. This study aimed to investigate the prognostic value of the mEASIX score in newly diagnosed cHL patients. Data from 206 patients who underwent positron emission tomography (PET)-guided doxorubicin, bleomycin, vinblastine, and dacarbazine (ABVD) therapy for cHL between January 2007 and November 2023 were retrospectively analyzed. The prognostic value of the mEASIX score was evaluated using the receiver operating characteristic (ROC) analysis, Cox regression analysis, and the Kaplan-Meier method, and then compared with standard risk assessment methods. The median age at diagnosis was 33 years, and the rate of patients in the advanced stage was 67%. ROC analysis determined an optimal mEASIX score cut-off of 17.28, categorizing patients into mEASIX (47%) and mEASIX (53%) groups. The 5-year progression-free survival (PFS) (60% vs. 84.3%) and overall survival (OS) (79.6% vs. 95.8%) were significantly lower in the mEASIX group ( < 0.001). Additionally, multivariate analysis showed that the independent variables affecting PFS included the nodular sclerosing subtype (HR: 0.4), bone marrow involvement (HR: 2.6), and elevated mEASIX (HR: 3.1). Independent variables, which had an effect on OS included elevated mEASIX (HR:3.8) and higher IPS-3 scores (HR:1.9). Furthermore, a higher mEASIX score (≥17.28) was identified as an independent variable indicating primary refractory disease (OR: 6.5). mEASIX is a powerful and easy-to-access marker for the detection of primary refractory disease and prognosis in newly diagnosed cHL cases.
尽管使用当前治疗方案,经典型霍奇金淋巴瘤(cHL)的治愈率高达90%,但原发性难治性患者的预后较差。因此,一种能够在诊断时预测早期进展患者的生物标志物是尚未满足的临床需求。内皮激活和应激指数(EASIX)及其变体改良EASIX(mEASIX)是目前用于预测血液系统恶性肿瘤预后的评分系统。本研究旨在探讨mEASIX评分在新诊断cHL患者中的预后价值。回顾性分析了2007年1月至2023年11月期间206例接受正电子发射断层扫描(PET)引导下多柔比星、博来霉素、长春碱和达卡巴嗪(ABVD)治疗cHL患者的数据。使用受试者工作特征(ROC)分析、Cox回归分析和Kaplan-Meier方法评估mEASIX评分的预后价值,然后与标准风险评估方法进行比较。诊断时的中位年龄为33岁,晚期患者比例为67%。ROC分析确定mEASIX评分的最佳临界值为17.28,将患者分为mEASIX(47%)和mEASIX(53%)组。mEASIX组的5年无进展生存期(PFS)(60%对84.3%)和总生存期(OS)(79.6%对95.8%)显著更低(<0.001)。此外,多因素分析显示影响PFS的独立变量包括结节硬化亚型(HR:0.4)、骨髓受累(HR:2.6)和mEASIX升高(HR:3.1)。影响OS的独立变量包括mEASIX升高(HR:3.8)和较高的国际预后评分系统(IPS)-3评分(HR:1.9)。此外,较高的mEASIX评分(≥17.28)被确定为指示原发性难治性疾病的独立变量(OR:6.5)。mEASIX是检测新诊断cHL病例中原发性难治性疾病和预后的一种强大且易于获取的标志物。