Clinicopathological analysis of primary intestinal diffuse large B‐cell lymphoma: Prognostic evaluation of CD5, PD‐L1, and Epstein‐Barr virus on tumor cells. (18th November 2018)

• Record Type: Journal Article
• Authors: Ishikawa, Eri; Kato, Seiichi; Shimada, Kazuyuki; Tanaka, Tsutomu; Suzuki, Yuka; Satou, Akira; Kohno, Kei; Sakakibara, Ayako; Yamamura, Takeshi; Nakamura, Masanao; Miyahara, Ryoji; Goto, Hidemi; Nakamura, Shigeo; Hirooka, Yoshiki
• Is Part Of: Cancer medicine. Volume 7:Number 12(2018:Dec.)
• Page Start: 6051
• Page End: 6063
• Publication Date: 2018-11-18
• Subjects: diffuse large B‐cell lymphoma -- Epstein‐Barr virus -- PD‐L1 -- primary intestinal lymphoma -- rituximab; 616.994005
• DOI: 10.1002/cam4.1875
• Languages: English
• ISSNs: 2045-7634

Abstract

Abstract: Background: Primary intestinal diffuse large B‐cell lymphoma (iDLBCL) is rare. In this study, we investigated the clinicopathological features of this disease to further understand the prognostic value of CD5, programmed cell death ligand 1 (PD‐L1), and Epstein‐Barr virus (EBV) on tumor cells. Methods: Tumor specimens from 62 patients consecutively diagnosed with primary iDLBCL at a single institution were analyzed. Results: Our series consisted of EBV‐positive (EBV + ) iDLBCL (n = 10), de novo CD5 + iDLBCL (n = 4), and DLBCL, not otherwise specified (DLBCL‐NOS; n = 48). Notably, seven of 10 EBV + cases had treated lymphoma‐associated (n = 4) or iatrogenic immunodeficiency (n = 3). Two of 10 EBV + cases expressed PD‐L1 on tumor cells, whereas the remaining eight were positive for PD‐L1 on microenvironment immune cells. Only one DLBCL‐NOS case had neoplastic PD‐L1 expression with a giant cell‐rich appearance. Both EBV‐harboring and PD‐L1 expression on tumor cells, but not CD5, were associated with worse overall survival (OS) in iDLBCL patients receiving rituximab‐containing chemotherapy ( P = 0.0354, P = 0.0092, and P = 0.1097, respectively). Multivariate analysis identified PD‐L1 positivity on tumor cells ( P = 0.0106), PD‐L1 negativity on microenvironment immune cells ( P = 0.0193), and EBV positivity ( P = 0.0324) as poor independent prognostic factors for OS. Among iDLBCL cases without any EBV association, CD5 positivity, or neoplastic PD‐L1 expression, high PD‐L1 expression (≥40%) on microenvironment immune cells predicted an extremely favorable outcome. Conclusion: EBV + iDLBCL mainly comprised immunodeficiency‐associated patients, which may highlight the specificity of the intestine. PD‐L1 expression on tumor cells or microenvironment immune cells was found to have an opposite prognostic impact in iDLBCL. Abstract : Both EBV‐harboring and PD‐L1 expression on tumor cells are associated with poor prognosis in primary iDLBCL, respectively. Primary iDLBCL patients with high PD‐L1 expression on immune cells have a good outcome, with the exception of CD5 +, EBV +, and nPD‐L1 + cases.