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Inherent PD-L1 22C3 Expression in Alveolar Macrophages Impacts the Combined Positive Score Status in Breast Cancer With Pulmonary Metastasis
DC Field | Value | Language |
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dc.contributor.author | 구자승 | - |
dc.contributor.author | 김혜민 | - |
dc.contributor.author | 차윤진 | - |
dc.date.accessioned | 2025-05-02T00:14:53Z | - |
dc.date.available | 2025-05-02T00:14:53Z | - |
dc.date.issued | 2025-03 | - |
dc.identifier.issn | 1759-7706 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/205325 | - |
dc.description.abstract | Purpose: This study aimed to determine the impact of inherent programmed death-ligand 1 (PD-L1)-expressing alveolar macrophages (AMs) on the combined positive score (CPS) of PD-L1 (22C3) in metastatic breast cancer in the lungs. Methods: A total of 87 patients with pulmonary metastases of breast cancer were included in this study. Immunohistochemical staining of various PD-L1 antibodies was performed. The CPSs and CPSs excluding the number of PD-L1 positive AMs [CPS(NAM)s] with PD-L1 (22C3) were determined and compared. Results: Among 87 enrolled patients, 22 had luminal A breast cancer, 24 had luminal B breast cancer, 13 had HER-2-positive breast cancer, and 28 had triple-negative breast cancer (TNBC). CPSs ≥ 10 was observed only in luminal B (12.5%) and TNBC (35.7%) subtypes (p < 0.001), whereas CPS(NAM)s ≥ 10 was observed only in TNBC (14.3%) (p = 0.011). Changes from the CPS-positive to the CPS(NAM)-negative status occurred in nine cases (10.3%), with significantly higher proportions being observed in the luminal B (12.5%) and TNBC (21.4%) subtypes (p = 0.007). Tumors showing changes from the CPS-positive to the CPS(NAM)-negative status were larger (p < 0.001); similar findings were observed in the TNBC subgroup (p = 0.001). Conclusion: The inclusion of PD-L1 expressing AMs leads to differences in CPS positivity, especially in large TNBC subtype tumors. | - |
dc.description.statementOfResponsibility | open | - |
dc.language | English | - |
dc.publisher | Wiley Publishing Asia Pty Ltd ; Tianjin Lung Cancer Institute | - |
dc.relation.isPartOf | THORACIC CANCER | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.subject.MESH | Adult | - |
dc.subject.MESH | Aged | - |
dc.subject.MESH | B7-H1 Antigen* / metabolism | - |
dc.subject.MESH | Biomarkers, Tumor / metabolism | - |
dc.subject.MESH | Breast Neoplasms* / metabolism | - |
dc.subject.MESH | Breast Neoplasms* / pathology | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Lung Neoplasms* / metabolism | - |
dc.subject.MESH | Lung Neoplasms* / pathology | - |
dc.subject.MESH | Macrophages, Alveolar* / metabolism | - |
dc.subject.MESH | Macrophages, Alveolar* / pathology | - |
dc.subject.MESH | Middle Aged | - |
dc.subject.MESH | Prognosis | - |
dc.title | Inherent PD-L1 22C3 Expression in Alveolar Macrophages Impacts the Combined Positive Score Status in Breast Cancer With Pulmonary Metastasis | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Pathology (병리학교실) | - |
dc.contributor.googleauthor | Yoon Jin Cha | - |
dc.contributor.googleauthor | Hye Min Kim | - |
dc.contributor.googleauthor | Ja Seung Koo | - |
dc.identifier.doi | 10.1111/1759-7714.70004 | - |
dc.contributor.localId | A00198 | - |
dc.contributor.localId | A04553 | - |
dc.contributor.localId | A04001 | - |
dc.relation.journalcode | J02725 | - |
dc.identifier.eissn | 1759-7714 | - |
dc.identifier.pmid | 40051246 | - |
dc.subject.keyword | PD‐L1 | - |
dc.subject.keyword | alveolar macrophages | - |
dc.subject.keyword | breast cancer | - |
dc.subject.keyword | lung metastasis | - |
dc.contributor.alternativeName | Koo, Ja Seung | - |
dc.contributor.affiliatedAuthor | 구자승 | - |
dc.contributor.affiliatedAuthor | 김혜민 | - |
dc.contributor.affiliatedAuthor | 차윤진 | - |
dc.citation.volume | 16 | - |
dc.citation.number | 5 | - |
dc.citation.startPage | e70004 | - |
dc.identifier.bibliographicCitation | THORACIC CANCER, Vol.16(5) : e70004, 2025-03 | - |
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