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Comparative analysis of PD-L1 expression and tumor-infiltrating lymphocytes in metaplastic breast carcinoma and gynecologic carcinosarcoma: A single-institution retrospective study.
Lin, Michelle S; Monroig-Bosque, Paloma C; Coffey, Donna M; Haley, Susan L; Okoye, Ekene I; Deavers, Michael T; Schwartz, Mary R; Crumley, Suzanne M.
Afiliación
  • Lin MS; Department of Pathology and Genomic Medicine, Houston Methodist Hospital, 6565 Fannin St. M227, Houston, TX 77030, United States of America. Electronic address: mslin@houstonmethodist.org.
  • Monroig-Bosque PC; Department of Pathology and Genomic Medicine, Houston Methodist Hospital, 6565 Fannin St. M227, Houston, TX 77030, United States of America. Electronic address: pmonroig@hrplabs.com.
  • Coffey DM; Department of Pathology and Genomic Medicine, Houston Methodist Hospital, 6565 Fannin St. M227, Houston, TX 77030, United States of America. Electronic address: dcoffey@houstonmethodist.org.
  • Haley SL; Department of Pathology and Genomic Medicine, Houston Methodist Hospital, 6565 Fannin St. M227, Houston, TX 77030, United States of America. Electronic address: slhaley@houstonmethodist.org.
  • Okoye EI; Department of Pathology and Genomic Medicine, Houston Methodist Hospital, 6565 Fannin St. M227, Houston, TX 77030, United States of America. Electronic address: eiokoye@houstonmethodist.org.
  • Deavers MT; Department of Pathology and Genomic Medicine, Houston Methodist Hospital, 6565 Fannin St. M227, Houston, TX 77030, United States of America. Electronic address: mdeavers@houstonmethodist.org.
  • Schwartz MR; Department of Pathology and Genomic Medicine, Houston Methodist Hospital, 6565 Fannin St. M227, Houston, TX 77030, United States of America. Electronic address: mschwartz@houstonmethodist.org.
  • Crumley SM; Department of Pathology and Immunology, Washington University School of Medicine, Saint Louis, MO 63110, United States of America. Electronic address: crumley@wustl.edu.
Ann Diagn Pathol ; 73: 152360, 2024 Jul 14.
Article en En | MEDLINE | ID: mdl-39029301
ABSTRACT
Metaplastic breast carcinoma (MBC) and gynecologic carcinosarcoma (GCS) are rare, clinically aggressive cancers that demonstrate epithelial components and mesenchymal or sarcomatoid components. In this study, we assessed PD-L1 expression and tumor-infiltrating lymphocytes (TILs) in MBC and GCS. Overall, PD-L1 positivity using the SP142 clone was seen in 50 % of MBC and 51.9 % of GCS cases, with PD-L1 expression in tumor cells significantly higher in MBC cases (p = 0.034), and PD-L1 expression in immune cells similar in MBC and GCS cases. PD-L1 expression was significantly higher in epithelial components than in mesenchymal components in both MBC and GCS cases (p = 0.0005). TILs were low in the majority of MBC and GCS cases (≥ 10 %) and generally correlated with PD-L1 expression; however, many PD-L1 positive cases with low TILs were seen. PD-L1 expression using the 22C3 clone was additionally assessed, with positivity seen in 62.9 % of MBC cases and 30 % of GCS cases. Concordance between SP142 and 22C3 results was seen in 62.5 % of MBC cases and 80 % of GCS cases. Overall, our findings suggest that a subset of MBC and GCS cases may benefit from immune checkpoint inhibitor therapy. Our findings also illustrate unique aspects of PD-L1 expression patterns in these tumors which may harbor additional prognostic and therapeutic significance.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Ann Diagn Pathol Asunto de la revista: PATOLOGIA Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Ann Diagn Pathol Asunto de la revista: PATOLOGIA Año: 2024 Tipo del documento: Article