表达滤泡树突状细胞的Fc-Epsilon受体(CD23)是滤泡性淋巴瘤的主要预后因素

N. Falaleeva, E. Osmanov, N. Tupitsyn
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引用次数: 0

摘要

表达Fc-epsilon受体(CD23)的滤泡树突状细胞是滤泡性淋巴瘤的主要预后因素。Falaleeva N. A, Osmanov E. A, Tupitsyn N. N. N.俄罗斯联邦卫生部俄罗斯癌症研究中心总结:在232例滤泡性淋巴瘤(FL)患者中研究了表达FceRII或CD23 (FceRIIFDCs)的滤泡树突状细胞作为非肿瘤环境的组成部分。在87.5%的滤泡性淋巴瘤病例中发现fceriifdc,并与肿瘤生长的结节型相关(p = 0.000),但与淋巴瘤的细胞学分级无关。从组织学上看,FceRIIFDC与FL患者的临床预后因素(FLIPI指数)或骨髓受累没有关联。根据治疗结果,即CR频率、OS持续时间和PFS,肿瘤组织中fceriifdc的存在是一个独立的预后因素。fceriifdc阳性组患者骨髓受累显著恶化预后。我们提出了一种新的预后指标(FDC-IP),可以对以下患者组进行生化鉴定:无骨髓受累的fceriifdc阳性患者(预后良好),骨髓受累的fceriifdc阳性患者(预后中等),fceriifdc阴性患者(预后差)。3组的OS和PFS均有显著差异(p = 0.000)。这是根据淋巴瘤生化和其他临床参数评估FL肿瘤行为和治疗结果的可能性的第一个证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fc-Epsilon Receptor (CD23) Expressing Follicular Dendritic Cells as a Main Prognostic Factor in Follicular Lymphoma
Fc-epsilon receptor (CD23)-expressing follicular dendritic cells is a main prognostic factor in follicular lymphoma. Falaleeva N. A., Osmanov E. A., Tupitsyn N. N. Federal State Budgetary Institute N. N. Blokhin Russian Cancer Research Center, Health Ministry of Russian Federation, Moscow, Russia SUMMARY Follicular dendritic cells, expressing FceRII or CD23 (FceRIIFDCs) as a component of non-tumor environment have been studied in 232 follicular lymphoma (FL) patients. FceRIIFDCs were found in 87.5% of follicular lymphoma cases and were associated with a nodular pattern of tumor growth (p = 0.000), but not the cytological grade of lymphoma. There were no associations of FceRIIFDC with clinical prognostic factors (FLIPI indices) or with bone marrow involvement in FL patients by histology. The presence of FceRIIFDCs in tumor tissue was an independent prognostic factor according to treatment results, i.e. frequency of CR, duration of OS and PFS. Bone marrow involvement significantly worsened the prognosis in FceRIIFDC-positive group of patients. We suggest a new prognostic index (FDC-IP) that allows biochemical identification of the following patient groups: FceRIIFDC-positive patients without bone marrow involvement (good prognosis), FceRIIF-DC-positive patients with bone marrow involvement (intermediate prognosis), FceRIIFDC-negative patients (poor prognosis). These 3 groups significantly differ (p = 0.000) both in OS and in PFS. This is the first evidence of the possibility to assess tumor behavior and treatment results in FL according to lymphoma biochemical and other than clinical parameters.
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