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免疫逃逸相关结外大B细胞淋巴瘤:6例肿瘤性PD-L1阳性结外弥漫性大B细胞淋巴瘤患者的报告

Immune evasion-related extranodal large B-cell lymphoma: A report of six patients with neoplastic PD-L1-positive extranodal diffuse large B-cell lymphoma.

作者信息

Suzuki Yuka, Sakakibara Ayako, Shimada Kazuyuki, Shimada Satoko, Ishikawa Eri, Nakamura Shigeo, Kato Seiichi, Takahara Taishi, Asano Naoko, Satou Akira, Kohno Kei

机构信息

Department of Pathology and Laboratory Medicine, Nagoya University Hospital, Nagoya, Japan.

Department of Hematology and Oncology, Nagoya University Graduate School of Medicine, Nagoya, Japan.

出版信息

Pathol Int. 2019 Jan;69(1):13-20. doi: 10.1111/pin.12742. Epub 2019 Jan 2.

Abstract

We identified six patients with Epstein-Barr virus (EBV)-negative extranodal diffuse large B-cell lymphoma (DLBCL) and immunohistochemical expression of PD-L1 on their tumor cells by examining 283 DLBCL cases with the PD-L1 SP142 clone between 2015 and 2017. They consisted of two men and four women with a median age of 71 years, and were examined in an autopsy (n = 1) and biopsies from the adrenal gland (n = 2), skin (n = 1), pelvic cavity (n = 1), and kidney (n = 1). All showed a monomorphic population of large transformed B-cells leading to diagnoses of DLBCL with two intravascular large B-cell lymphoma (IVLBCL) and one de novo CD5+ type and were featured by an invariable immunephenotype: CD3-, CD20+, BCL-2+, and MUM1+. In addition, CD5 and CD10 were each detected in one case. All cases expressed PD-L1 on >10% to >90% of tumor cells, which was confirmed with two other PD-L1 antibodies (E1J2J and 28-8). Three untreated patients had a rapid, lethal clinical course within 7 months after diagnosis; while, the remaining three achieved complete remission after treatment and were alive at the last follow-up. We suggest immune evasion-related extranodal large B-cell lymphoma should be recognized beyond the currently identified entities of IVLBCL and de novo CD5+ DLBCL.

摘要

2015年至2017年期间,我们通过检测283例采用PD-L1 SP142克隆的弥漫性大B细胞淋巴瘤(DLBCL)病例,确定了6例 Epstein-Barr病毒(EBV)阴性的结外弥漫性大B细胞淋巴瘤患者,其肿瘤细胞上存在PD-L1免疫组化表达。他们包括2名男性和4名女性,中位年龄为71岁,接受了尸检(n = 1)以及来自肾上腺(n = 2)、皮肤(n = 1)、盆腔(n = 1)和肾脏(n = 1)的活检。所有病例均显示为大的转化B细胞单形性群体,诊断为DLBCL,其中2例为血管内大B细胞淋巴瘤(IVLBCL),1例为原发性CD5+型,其特征为免疫表型不变:CD3-、CD20+、BCL-2+和MUM1+。此外,各有1例检测到CD5和CD10。所有病例中,>10%至>90%的肿瘤细胞表达PD-L1,这通过另外两种PD-L1抗体(E1J2J和28-8)得以证实。3例未经治疗的患者在诊断后7个月内出现快速致命的临床病程;而其余3例在治疗后实现完全缓解,在最后一次随访时仍存活。我们建议,除了目前已确定的IVLBCL和原发性CD5+ DLBCL实体之外,还应认识到与免疫逃逸相关的结外大B细胞淋巴瘤。

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