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Clinical and genomic assessment of PD-L1 SP142 expression in triple-negative breast cancer

PURPOSE: The SP142 PD-L1 assay is a companion diagnostic for atezolizumab in metastatic triple-negative breast cancer (TNBC). We strove to understand the biological, genomic, and clinical characteristics associated with SP142 PD-L1 positivity in TNBC patients. METHODS: Using 149 TNBC formalin-fixed...

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Autores principales: Ahn, Sung Gwe, Kim, Seon-Kyu, Shepherd, Jonathan H., Cha, Yoon Jin, Bae, Soong June, Kim, Chungyeul, Jeong, Joon, Perou, Charles M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8233296/
https://www.ncbi.nlm.nih.gov/pubmed/33770313
http://dx.doi.org/10.1007/s10549-021-06193-9
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author Ahn, Sung Gwe
Kim, Seon-Kyu
Shepherd, Jonathan H.
Cha, Yoon Jin
Bae, Soong June
Kim, Chungyeul
Jeong, Joon
Perou, Charles M.
author_facet Ahn, Sung Gwe
Kim, Seon-Kyu
Shepherd, Jonathan H.
Cha, Yoon Jin
Bae, Soong June
Kim, Chungyeul
Jeong, Joon
Perou, Charles M.
author_sort Ahn, Sung Gwe
collection PubMed
description PURPOSE: The SP142 PD-L1 assay is a companion diagnostic for atezolizumab in metastatic triple-negative breast cancer (TNBC). We strove to understand the biological, genomic, and clinical characteristics associated with SP142 PD-L1 positivity in TNBC patients. METHODS: Using 149 TNBC formalin-fixed paraffin-embedded tumor samples, tissue microarray (TMA) and gene expression microarrays were performed in parallel. The VENTANA SP142 assay was used to identify PD-L1 expression from TMA slides. We next generated a gene signature reflective of SP142 status and evaluated signature distribution according to TNBCtype and PAM50 subtypes. A SP142 gene expression signature was identified and was biologically and clinically evaluated on the TNBCs of TCGA, other cohorts, and on other malignancies treated with immune checkpoint inhibitors (ICI). RESULTS: Using SP142, 28.9% of samples were PD-L1 protein positive. The SP142 PD-L1-positive TNBC had higher CD8+ T cell percentage, stromal tumor-infiltrating lymphocyte levels, and higher rate of the immunomodulatory TNBCtype compared to PD-L1-negative samples. The recurrence-free survival was prolonged in PD-L1-positive TNBC. The SP142-guided gene expression signature consisted of 94 immune-related genes. The SP142 signature was associated with a higher pathologic complete response rate and better survival in multiple TNBC cohorts. In the TNBC of TCGA, this signature was correlated with lymphocyte-infiltrating signature scores, but not with tumor mutational burden or total neoantigen count. In other malignancies treated with ICIs, the SP142 genomic signature was associated with improved response and survival. CONCLUSIONS: We provide multi-faceted evidence that SP142 PDL1-positive TNBC have immuno-genomic features characterized as highly lymphocyte-infiltrated and a relatively favorable survival. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10549-021-06193-9.
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spelling pubmed-82332962021-07-09 Clinical and genomic assessment of PD-L1 SP142 expression in triple-negative breast cancer Ahn, Sung Gwe Kim, Seon-Kyu Shepherd, Jonathan H. Cha, Yoon Jin Bae, Soong June Kim, Chungyeul Jeong, Joon Perou, Charles M. Breast Cancer Res Treat Clinical Trial PURPOSE: The SP142 PD-L1 assay is a companion diagnostic for atezolizumab in metastatic triple-negative breast cancer (TNBC). We strove to understand the biological, genomic, and clinical characteristics associated with SP142 PD-L1 positivity in TNBC patients. METHODS: Using 149 TNBC formalin-fixed paraffin-embedded tumor samples, tissue microarray (TMA) and gene expression microarrays were performed in parallel. The VENTANA SP142 assay was used to identify PD-L1 expression from TMA slides. We next generated a gene signature reflective of SP142 status and evaluated signature distribution according to TNBCtype and PAM50 subtypes. A SP142 gene expression signature was identified and was biologically and clinically evaluated on the TNBCs of TCGA, other cohorts, and on other malignancies treated with immune checkpoint inhibitors (ICI). RESULTS: Using SP142, 28.9% of samples were PD-L1 protein positive. The SP142 PD-L1-positive TNBC had higher CD8+ T cell percentage, stromal tumor-infiltrating lymphocyte levels, and higher rate of the immunomodulatory TNBCtype compared to PD-L1-negative samples. The recurrence-free survival was prolonged in PD-L1-positive TNBC. The SP142-guided gene expression signature consisted of 94 immune-related genes. The SP142 signature was associated with a higher pathologic complete response rate and better survival in multiple TNBC cohorts. In the TNBC of TCGA, this signature was correlated with lymphocyte-infiltrating signature scores, but not with tumor mutational burden or total neoantigen count. In other malignancies treated with ICIs, the SP142 genomic signature was associated with improved response and survival. CONCLUSIONS: We provide multi-faceted evidence that SP142 PDL1-positive TNBC have immuno-genomic features characterized as highly lymphocyte-infiltrated and a relatively favorable survival. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10549-021-06193-9. Springer US 2021-03-26 2021 /pmc/articles/PMC8233296/ /pubmed/33770313 http://dx.doi.org/10.1007/s10549-021-06193-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Clinical Trial
Ahn, Sung Gwe
Kim, Seon-Kyu
Shepherd, Jonathan H.
Cha, Yoon Jin
Bae, Soong June
Kim, Chungyeul
Jeong, Joon
Perou, Charles M.
Clinical and genomic assessment of PD-L1 SP142 expression in triple-negative breast cancer
title Clinical and genomic assessment of PD-L1 SP142 expression in triple-negative breast cancer
title_full Clinical and genomic assessment of PD-L1 SP142 expression in triple-negative breast cancer
title_fullStr Clinical and genomic assessment of PD-L1 SP142 expression in triple-negative breast cancer
title_full_unstemmed Clinical and genomic assessment of PD-L1 SP142 expression in triple-negative breast cancer
title_short Clinical and genomic assessment of PD-L1 SP142 expression in triple-negative breast cancer
title_sort clinical and genomic assessment of pd-l1 sp142 expression in triple-negative breast cancer
topic Clinical Trial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8233296/
https://www.ncbi.nlm.nih.gov/pubmed/33770313
http://dx.doi.org/10.1007/s10549-021-06193-9
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