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未另行指定的CD20阳性外周T细胞淋巴瘤:病例系列及文献复习

CD20-positive peripheral T-cell lymphoma not otherwise specified: a case series and review of the literature.

作者信息

Zhou Pan, Wang Lifu, Pei Xiaohang, Yang Liu, Zhou Yunmeng, Ma Rongjun, Chen Yuqing, Zhu Zunmin, Yuan Xiaoli

机构信息

Department of Hematology, Henan Provincial People's Hospital, Zhengzhou University People's Hospital, Zhengzhou, China.

Department of Pathology, Henan Provincial People's Hospital, Zhengzhou University People's Hospital, Zhengzhou, China.

出版信息

Front Oncol. 2025 Apr 9;15:1553969. doi: 10.3389/fonc.2025.1553969. eCollection 2025.

Abstract

Peripheral T-cell lymphoma not otherwise specified (PTCL-NOS) is a heterogeneous and aggressive malignancy that usually lacks B-cell associated antigens. Here, we identified three cases of PTCL-NOS that uniformly expressed T-cell specific antigens (CD2 and CD3) and the B marker CD20 (CD20+ PTCL-NOS). Molecular studies showed clonal rearrangement of the chain T-cell receptor genes without evidence of a clonal rearrangement of the immunoglobulin gene. All three patients were diagnosed with the advanced stages and had bone marrow (BM) involvement, of which one patient was confirmed by PET-CT and the other two patients were confirmed by BM biopsy. However, we surprisingly found that BM-infiltrated lymphoma cells did not express CD20. Whole-exome sequencing analysis revealed that the most common mutations were on the and genes. Although all the patients had relatively low Ki67 indices, they achieved poor response to the first-line treatment with CHOP-like chemotherapy. Subsequently, one patient was treated at a local hospital with an unspecified regimen, and the other two patients ultimately received rituximab combined chemotherapy as a salvage treatment after receiving multiple second-line therapies. However, the outcomes of these patients remained unsatisfactory. Therefore, it currently appears to be quite challenging to provide appropriate and effective treatment for patients with CD20+ PTCL-NOS.

摘要

外周T细胞淋巴瘤,非特殊类型(PTCL-NOS)是一种异质性侵袭性恶性肿瘤,通常缺乏B细胞相关抗原。在此,我们鉴定出3例PTCL-NOS病例,这些病例均表达T细胞特异性抗原(CD2和CD3)以及B细胞标志物CD20(CD20+ PTCL-NOS)。分子研究显示T细胞受体基因的链存在克隆重排,而免疫球蛋白基因无克隆重排证据。所有3例患者均诊断为晚期且有骨髓(BM)受累,其中1例经PET-CT证实,另外2例经BM活检证实。然而,我们意外地发现BM浸润的淋巴瘤细胞不表达CD20。全外显子测序分析显示,最常见的突变位于和基因上。尽管所有患者的Ki67指数相对较低,但他们对CHOP样一线化疗反应不佳。随后,1例患者在当地医院接受了未明确的治疗方案,另外2例患者在接受多种二线治疗后最终接受利妥昔单抗联合化疗作为挽救治疗。然而,这些患者的结局仍不尽人意。因此,目前为CD20+ PTCL-NOS患者提供恰当有效的治疗似乎颇具挑战性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5993/12014747/193fed0612f8/fonc-15-1553969-g001.jpg

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