Prognostic Implication of Programmed Death-1-Positive Tumor-infiltrating Lymphocytes in Diffuse Large B-Cell Lymphoma
- Authors
- Ko, Young Sin; Oh, Young Ha; Park, Chan Kum; Kim, Wook Youn; Han, Hye Seung; Lim, So Dug; Hwang, Tae Sook; Kim, Wan Seop
- Issue Date
- Dec-2011
- Publisher
- Korean Society of Pathologists
- Keywords
- Lymphoma, large B-cell, diffuse; Programmed death-1 (PD-1); Lymphoma; Prognostic factor
- Citation
- Korean Journal of Pathology, v.45, no.6, pp 573 - 581
- Pages
- 9
- Indexed
- SCIE
SCOPUS
- Journal Title
- Korean Journal of Pathology
- Volume
- 45
- Number
- 6
- Start Page
- 573
- End Page
- 581
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/166977
- DOI
- 10.4132/KoreanJPathol.2011.45.6.573
- ISSN
- 1738-1843
2092-8920
- Abstract
- Background: Programmed death-1 (PD-1) is physiologically expressed by germinal center-associated helper T-cells and has an inhibitory effect on T-cell activity. Methods: We examined 63 cases of diffuse large B-cell lymphoma (DLBCL) and determined the number of PD-1-positive helper T-cells in a representative tumor area after immunohistochemical staining using a monoclonal antibody against PD-1. The PD-1-positive cells were counted in 3 high-power fields (HPFs; 400 x). Results: Patients were divided into 2 groups: one with a high number of PD-1-positive cells (> 20/HPF, n=33) and one with a low number of PD-1-positive cells (<= 20/HPF, n=30). The former group showed decreased overall survival, but at a statistically non-significant level (p=0.073). A high number of PD-1-positive cells was more common in patients at an advanced clinical stage and with high international prognostic index score (p=0.025 and p=0.026, respectively). The number of extranodal sites also somewhat correlated with the PD-1 staining status (p=0.071). However, the number of PD-1-positive cells was not associated with patient age, serum lactate dehydrogenase level, and Eastern Cooperative Oncology Group performance score. Conclusions: The high number of PD-1-positive cells might be associated with an unfavorable outcome in DLBCL patients.
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