Prognostic implications of the tumor immune microenvironment and immune checkpoint pathway in primary central nervous system diffuse large B‐cell lymphoma in the North Indian population. Issue 2 (23rd December 2021)

• Record Type: Journal Article
• Authors: Parkhi, Mayur; Chatterjee, Debajyoti; Bal, Amanjit; Vias, Poorva; Yadav, Budhi Singh; Prakash, Gaurav; Gupta, Sunil Kumar; Radotra, Bishan Dass
• Is Part Of: Apmis. Volume 130:Issue 2(2022)
• Page Start: 82
• Page End: 94
• Publication Date: 2021-12-23
• Subjects: Central nervous system -- diffuse large B‐cell lymphoma -- tumor microenvironment -- PD‐L1 -- tumor‐infiltrating lymphocytes; Pathology -- Periodicals; Microbiology -- Periodicals; Immunology -- Periodicals; 572
• DOI: 10.1111/apm.13195
• Languages: English
• ISSNs: 0903-4641

Abstract

Abstract : Primary central nervous system‐diffuse large B‐cell lymphoma (PCNS‐DLBCL) is a rare, extranodal malignant lymphoma carrying poor prognosis. The prognostic impact of tumor microenvironment (TME) composition and the PD‐1/PD‐L1 immune checkpoint pathway are still undetermined in PCNS‐DLBCL. We aimed to quantify the tumor‐infiltrating lymphocytes (TILs), tumor‐associated macrophages (TAMs), and PD‐L1 expression in the PCNSL and evaluated their prognostic significance. All patients with histopathologically diagnosed PCNS‐DLBCL over a period of 7 years were recruited. Immunohistochemistry for CD3, CD4, CD8, FOXP3, CD68, CD163, PD‐1, and PD‐L1 was performed on the tissue microarray. Forty‐four cases of PCNS‐DLBCL, who satisfied the selection criteria, were included with mean age of 55 ± 12.3 years and male‐to‐female ratio of 0.91:1. The mean overall survival (OS) and disease‐free survival (DFS) was 531.6 days and 409.8 days, respectively. Among TILs, an increased number of CD3+ T cells showed better OS and DFS, without achieving statistical significance. CD4 positive T‐cells were significantly associated with the longer OS (p = 0.037) and DFS (p = 0.023). TAMs (68CD and CD163 positive) showed an inverse relationship with OS and DFS but did not reach statistical significance (p > 0.05). Increased PD‐L1 expression in immune cells, but not in tumor cells, was associated with significantly better DFS (p = 0.037). The TME plays a significant role in the prognosis of PCNS‐DLBCL. Increased number of CD4+ T cells and PD‐L1–expressing immune cells is associated with better prognosis in PCNS‐DLBCL. Further studies with larger sample size are required to evaluate the role of targeted therapy against the TME and immune check point inhibitors in this disease.