4.3 Article

Expression of Programmed Death Ligand 1 (PD-L1) in Posttreatment Primary Inflammatory Breast Cancers and Clinical Implications

期刊

AMERICAN JOURNAL OF CLINICAL PATHOLOGY
卷 149, 期 3, 页码 253-261

出版社

OXFORD UNIV PRESS INC
DOI: 10.1093/AJCP/AQX162

关键词

PD-L1; Inflammatory breast cancer; Survival; Prognosis; Breast; Immunohistochemistry

资金

  1. faculty research fund of The University of Texas MD Anderson Cancer Center
  2. NATIONAL CANCER INSTITUTE [P30CA016672] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Objectives: Inflammatory breast carcinoma (IBC) is rare but is the most lethal type of breast cancer. Programmed death ligand 1 (PD-L1) expression in IBCs has been understudied. Methods: In this study, tissue microarrays of 68 IBCs were immunostained with a PD-L1 antibody using an antibody clone (28-8) and detection system approved by the US Food and Drug Administration for selecting patients with non-small cell lung cancer and melanoma for anti-PD-L1 therapy. Results: Positive PD-L1 expression was found in 25 (36.8%) of 68 samples but was not significantly associated with the clinicopathologic variables examined. Univariate analysis of overall survival (OS) revealed that worse OS was significantly associated with positive PD-L1, negative estrogen receptor, and triple-negative status. The 5-year OS rate was 36.4% for patients with PD-L1-positive IBC and 47.3% for those with PD-L1-negative IBC. In multivariate analyses, PD-L1 status remained a statistically independent predictor of OS. Conclusions: These findings indicate that PD-L1 inhibitors could potentially improve the clinical outcome of patients with PD-L1-positive IBC.

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