PD‐L1 (SP142) expression in neoplastic cells predicts a poor prognosis for patients with intravascular large B‐cell lymphoma treated with rituximab‐based multi‐agent chemotherapy Article Swipe
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· 2020
· Open Access
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· DOI: https://doi.org/10.1002/cam4.3104
Background Intravascular large B‐cell lymphoma (IVLBCL) is a rare form of diffuse large B‐cell lymphoma (DLBCL) arising in extranodal sites. PD‐L1 expression of tumor cells has been reported in IVLBCL cells, but its clinicopathological relevance remains to be elucidated. Aims This study was aimed to reveal the characteristics of PD‐L1 + IVLBCL. Methods and results Neoplastic PD‐L1 expression was examined in 34 cases of IVLBCL and clinicopathological characteristics between patients with PD‐L1 + and PD‐L1 − IVLBCL were compared. We assessed PD‐L1 expression with SP142 antibody. Twelve (35%) of 34 cases showed positivity for PD‐L1. The PD‐L1 + group had significantly lower survival rates compared to the PD‐L1 − group. The PD‐L1 + IVLBCL group also had a significantly lower age distribution and a lower frequency of patients older than 60 years compared to the PD‐L1 − group. Very recently, we speculate that there is possible link between PD‐L1 + IVLBCL and PD‐L1 + extranodal DLBCL‐NOS (eDLBCL) because features of the two groups showed overlapping. Therefore, we compared the clinicopathological characteristics of the PD‐L1 + IVLBCL and PD‐L1 + eDLBCL. There were no significant differences in clinicopathological parameters and prognosis. Conclusion The worse prognosis of the PD‐L1 + group might be caused by immune evasion mechanisms, which are linked to PD‐L1 expression. Therefore, PD‐L1 + IVLBCL cases might be regarded as good candidates for targeted immunotherapy. We also highlighted the overlapping features of PD‐L1 + IVLBCL and PD‐L1 + eDLBCL. This result suggests that they should be regarded as one entity, immune evasion‐related extranodal large B‐cell lymphoma.
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- Type
- article
- Language
- en
- Landing Page
- https://doi.org/10.1002/cam4.3104
- https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/cam4.3104
- OA Status
- gold
- Cited By
- 19
- References
- 51
- Related Works
- 10
- OpenAlex ID
- https://openalex.org/W3023407502
Raw OpenAlex JSON
- OpenAlex ID
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https://openalex.org/W3023407502Canonical identifier for this work in OpenAlex
- DOI
-
https://doi.org/10.1002/cam4.3104Digital Object Identifier
- Title
-
PD‐L1 (SP142) expression in neoplastic cells predicts a poor prognosis for patients with intravascular large B‐cell lymphoma treated with rituximab‐based multi‐agent chemotherapyWork title
- Type
-
articleOpenAlex work type
- Language
-
enPrimary language
- Publication year
-
2020Year of publication
- Publication date
-
2020-05-05Full publication date if available
- Authors
-
Yuka Suzuki, Kei Kohno, Kosei Matsue, Ayako Sakakibara, Eri Ishikawa, Satoko Shimada, Kazuyuki Shimada, Seiyo Mabuchi, Taishi Takahara, Seiichi Kato, Shigeo Nakamura, Akira SatouList of authors in order
- Landing page
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https://doi.org/10.1002/cam4.3104Publisher landing page
- PDF URL
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https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/cam4.3104Direct link to full text PDF
- Open access
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YesWhether a free full text is available
- OA status
-
goldOpen access status per OpenAlex
- OA URL
-
https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/cam4.3104Direct OA link when available
- Concepts
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Intravascular large B-cell lymphoma, Lymphoma, Immunohistochemistry, Medicine, PD-L1, Rituximab, Chemotherapy, Immune system, Immunotherapy, Pathology, Internal medicine, Cancer research, ImmunologyTop concepts (fields/topics) attached by OpenAlex
- Cited by
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19Total citation count in OpenAlex
- Citations by year (recent)
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2025: 3, 2024: 2, 2023: 2, 2022: 3, 2021: 6Per-year citation counts (last 5 years)
- References (count)
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51Number of works referenced by this work
- Related works (count)
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10Other works algorithmically related by OpenAlex
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| corresponding_author_ids | https://openalex.org/A5059183289 |
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| institutions_distinct_count | 12 |
| corresponding_institution_ids | https://openalex.org/I4210099598 |
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| citation_normalized_percentile.is_in_top_10_percent | False |