不适合移植的大 B 细胞淋巴瘤二线使用 axicabtagene ciloleucel:ALYCANTE 最终分析
Second-line axicabtagene ciloleucel in large B-cell lymphoma ineligible for transplantation: ALYCANTE final analysis.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Primary gastric EBV-positive cytotoxic-molecule-negative T-cell lymphoma with TET2 multihit mutations: a case report.
Primary gastric EBV-positive cytotoxic-molecule-negative T-cell lymphoma with TET2 multihit mutations: a case report.
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结外NK/T细胞淋巴瘤(ENKTL)是一种EBV阳性的NK细胞或细胞毒性T细胞谱系淋巴瘤。根据世界卫生组织造血淋巴肿瘤分类第五版(WHO-HAEM5),缺乏细胞毒性分子的EBV阳性病例不能归类为ENKTL。据我们所知,这是首例记录在案的原发性胃EBV阳性T细胞淋巴瘤且不表达细胞毒性分子的病例。一名76岁女性最初表现为病变局限于胃,随后连续性延伸至十二指肠。活检显示小至中等大小的非典型T细胞,胞质淡染,核不规则折叠,并伴有血管内浸润。肿瘤细胞CD3、TCRβF1和CD4阳性,CD56、TIA-1、颗粒酶B、穿孔素和PD-L1阴性。EBV编码RNA原位杂交突出显示了肿瘤性T细胞。这些发现不符合WHO-HAEM5中任何T/NK细胞实体的标准,包括ENKTL和非特指型外周T细胞淋巴瘤(PTCL, NOS)。靶向测序显示TET2多重打击突变,提示克隆性造血相关发病机制。鉴于患者年龄和肿瘤位置,我们给予减量DeVIC方案,随后放疗,获得部分缓解。该病例扩展了EBV相关T细胞淋巴瘤的谱系,并强调需要更多病例来完善分类和管理。
Extranodal NK/T-cell lymphoma (ENKTL) is an Epstein-Barr virus (EBV)-positive lymphoma of the NK- or cytotoxic T-cell lineage. According to the World Health Organization Classification of Hematolymphoid Tumors, Fifth Edition (WHO-HAEM5), EBV-positive cases lacking cytotoxic molecules cannot be classified as ENKTL. To the best of our knowledge, this is the first documented case of primary gastric EBV-positive T-cell lymphoma lacking the expression of cytotoxic molecules.
A 76-year-old woman initially presented with a disease confined to the stomach, with subsequent contiguous extension into the duodenum. Biopsies revealed small- to medium-sized atypical T cells with pale cytoplasm and irregularly folded nuclei, as well as intravascular infiltration. Tumor cells were positive for CD3, TCRβF1, and CD4 and negative for CD56, TIA-1, granzyme B, perforin, and PD-L1. EBV-encoded RNA in situ hybridization highlighted neoplastic T cells.
These findings did not fulfill the criteria for any T/NK cell entity of WHO-HAEM5 including ENKTL and peripheral T-cell lymphoma not otherwise specified (PTCL, NOS). Targeted sequencing revealed TET2 multihit mutations, suggesting clonal hematopoiesis-linked pathogenesis.
Given the patient's age and tumor location, we administered a reduced dose of DeVIC, followed by radiotherapy, achieving partial remission. This case expands the spectrum of EBV-associated T-cell lymphomas and highlights the need for additional cases to refine the classification and management.
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