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日本队列中肿瘤 PD-L1 阳性 EBV 弥漫性大 B 细胞淋巴瘤,非特指型的临床病理分析。

Clinicopathological analysis of neoplastic PD-L1-positive EBV diffuse large B cell lymphoma, not otherwise specified, in a Japanese cohort.

机构信息

Department of Surgical Pathology, Aichi Medical University Hospital, 1-1, Yazakokarimata, Nagakute, 480-1195, Japan.

Department of Gastroenterology and Hepatology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

出版信息

Virchows Arch. 2021 Mar;478(3):541-552. doi: 10.1007/s00428-020-02901-w. Epub 2020 Aug 15.

Abstract

The programmed death 1 (PD1)/PD1 ligand (PD-L1) axis plays an important role in the pathogenesis of Epstein-Barr virus-positive diffuse large B cell lymphoma, not otherwise specified (EBV+ DLBCL, NOS). Here, we describe PD-L1 expression by EBV+ DLBCL, NOS in order to evaluate its possible contribution to the pathogenesis of this tumor. The study included 57 cases of EBV+ DLBCL, NOS. The median patient age was 69 years and 95% (n = 54) were aged > 45. Extranodal lesions were present in 39 (69%) at initial diagnosis. PD-L1 expression (mAb SP142-positive staining) was present in more than 5% of tumor cells in only six cases (11%), in clear contrast to the 77% reported in cases aged under 45 years. Among the PD-L1+ cases, three were nodal lesions. All six PD-L1+ cases progressed in the 3 years after diagnosis and four of the six patients died of the disease within 2 years. PD-L1+ cases had significantly shorter PFS (P = 0.002) and relatively short OS (P = 0.26), compared with PD-L1- cases. EBV+ DLBCL, NOS in the elderly infrequently expressed PD-L1 and had poor prognosis. PD-L1 expression in EBV+ DLBCL, NOS of the elderly sheds light on the pathogenetic role of immune senescence.

摘要

程序性死亡受体 1(PD1)/PD1 配体(PD-L1)轴在 EBV 阳性弥漫性大 B 细胞淋巴瘤,非特指型(EBV+ DLBCL,NOS)的发病机制中起着重要作用。在此,我们描述了 EBV+ DLBCL,NOS 中的 PD-L1 表达,以评估其对这种肿瘤发病机制的可能贡献。该研究包括 57 例 EBV+ DLBCL,NOS。患者中位年龄为 69 岁,95%(n=54)年龄大于 45 岁。初次诊断时,39 例(69%)存在结外病变。只有 6 例(11%)肿瘤细胞中 PD-L1 表达(SP142 单抗阳性染色)超过 5%,与 45 岁以下病例报道的 77%形成鲜明对比。在 PD-L1+病例中,有 3 例为淋巴结病变。在诊断后 3 年内,所有 6 例 PD-L1+病例均进展,其中 6 例患者中的 4 例在 2 年内死于该疾病。与 PD-L1-病例相比,PD-L1+病例的 PFS(P=0.002)明显更短,OS 相对较短(P=0.26)。老年 EBV+ DLBCL,NOS 很少表达 PD-L1,预后不良。老年 EBV+ DLBCL,NOS 中 PD-L1 的表达揭示了免疫衰老在发病机制中的作用。

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