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基于 VEGF 和国际预后指数的风险分层模型可准确识别利妥昔单抗时代的低危弥漫性大 B 细胞淋巴瘤患者。

Risk stratification model based on VEGF and International Prognostic Index accurately identifies low-risk diffuse large B-cell lymphoma patients in the rituximab era.

机构信息

Department of Hematology, Affiliated Hospital of Xuzhou Medical University, Xuzhou, 221002, Jiangsu, China.

Department of Epidemiology and Biostatistics, School of Public Health, Xuzhou Medical University, Xuzhou, 221004, Jiangsu, China.

出版信息

Int J Hematol. 2021 Aug;114(2):189-198. doi: 10.1007/s12185-021-03145-3. Epub 2021 Apr 24.

Abstract

Vascular endothelial growth factor affects the invasiveness of solid tumors by regulating angiogenesis. However, it is not clear whether VEGF could be used to predict the prognosis of DLBCL in the era of rituximab-based immunotherapy. We conducted a retrospective study to explore response to therapy and the prognostic value of VEGF on DLBCL in the rituximab era. The subjects were 65 patients with a histological diagnosis of DLBCL from the Affiliated Hospital of Xuzhou Medical University. Kaplan-Meier analysis was performed to estimate the cumulative survival rate of patients with different VEGF and IPI levels, and comparisons between groups were made using the log-rank test. DLBCL patients with elevated VEGF were more likely to have extranodal involvement, advanced stage, Myc/Bcl-2 double expression, and a higher Ki-67 score. Elevated VEGF was associated with poor therapeutic response and survival. When patients were divided into low, low-intermediate, high-intermediate and high-risk groups using the V-IPI model based on VEGF and IPI, PFS rates were 94.4, 74.1, 40.6 and 14.8%, respectively. This model better identified low-risk patients than IPI (85.9, 88.9, 37 and 7.8%). Our results demonstrate that VEGF predicts therapeutic response in DLBCL and the V-IPI model accurately predicts PFS of low-risk DLBCL in the rituximab era.

摘要

血管内皮生长因子通过调节血管生成影响实体瘤的侵袭性。然而,在利妥昔单抗为基础的免疫治疗时代,VEGF 是否可用于预测 DLBCL 的预后尚不清楚。我们进行了一项回顾性研究,以探讨 VEGF 在利妥昔单抗时代对 DLBCL 治疗反应和预后价值。研究对象为来自徐州医科大学附属医院的 65 例组织学诊断为 DLBCL 的患者。Kaplan-Meier 分析用于估计不同 VEGF 和 IPI 水平患者的累积生存率,对数秩检验用于组间比较。VEGF 升高的 DLBCL 患者更有可能出现结外受累、晚期、Myc/Bcl-2 双重表达和更高的 Ki-67 评分。VEGF 升高与治疗反应不良和生存不良相关。当根据 VEGF 和 IPI 将患者分为低、低中、高中和高危组时,PFS 率分别为 94.4%、74.1%、40.6%和 14.8%。该模型比 IPI (85.9%、88.9%、37%和 7.8%)更好地识别低危患者。我们的研究结果表明,VEGF 可预测 DLBCL 的治疗反应,V-IPI 模型可准确预测利妥昔单抗时代低危 DLBCL 的 PFS。

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