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

被引:22
|
作者
Suzuki, Yuka [1 ]
Sakakibara, Ayako [1 ]
Shimada, Kazuyuki [2 ]
Shimada, Satoko [1 ]
Ishikawa, Eri [1 ,3 ]
Nakamura, Shigeo [1 ]
Kato, Seiichi [4 ]
Takahara, Taishi [5 ]
Asano, Naoko [6 ]
Satou, Akira [5 ]
Kohno, Kei [1 ]
机构
[1] Nagoya Univ Hosp, Dept Pathol & Lab Med, Nagoya, Aichi, Japan
[2] Nagoya Univ, Grad Sch Med, Dept Hematol & Oncol, Nagoya, Aichi, Japan
[3] Nagoya Univ, Grad Sch Med, Dept Gastroenterol & Hepatol, Nagoya, Aichi, Japan
[4] Aichi Canc Ctr Hosp, Dept Pathol & Mol Diagnost, Nagoya, Aichi, Japan
[5] Aichi Med Univ Hosp, Dept Surg Pathol, Nagakute, Aichi, Japan
[6] Nagano Prefectural Shinshu Med Ctr, Dept Clin Lab, Suzaka, Japan
基金
日本学术振兴会;
关键词
de novo CD5+diffuse large B-cell lymphoma; extranodal diffuse large B-cell lymphoma; immune evasion; intravascular large B-cell lymphoma; neoplastic PD-L1 expression; DEATH LIGAND 1; RETROSPECTIVE ANALYSIS; PROGNOSTIC-FACTORS; PDL1; EXPRESSION; HIGH-FREQUENCY; LEG TYPE; RITUXIMAB; PD-L1; CHEMOTHERAPY; MANAGEMENT;
D O I
10.1111/pin.12742
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
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.
引用
收藏
页码:13 / 20
页数:8
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