Responses to checkpoint inhibition in metastatic triple negative breast cancer driven by divergent myeloid phenotypes

Our findings highlight CD33<sup>+</sup> cell phenotype as a key determinant of response to chemo-immunotherapy, which can be assessed from peripheral blood. This offers a valuable tool in the context of metastatic TNBC, in which tissue sampling is often challenging.

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Publication Details

Journal
Communications Medicine
Published
2025-05-17
DOI
https://doi.org/10.1038/s43856-025-00860-4
Citations
2
Primary Topic
Cancer Genomics and Diagnostics
Type
article
Field-Weighted Citation Impact
1.87
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article

Responses to checkpoint inhibition in metastatic triple negative breast cancer driven by divergent myeloid phenotypes

Avia D. Wilkerson, Patricia Rayman, Tyler Alban, Zahraa Al‐Hilli et al.
2 citations
Communications Medicine
Cancer Genomics and Diagnostics
1.87
article

Responses to checkpoint inhibition in metastatic triple negative breast cancer driven by divergent myeloid phenotypes

Avia D. Wilkerson, Patricia Rayman, Tyler Alban, Zahraa Al‐Hilli, Alberto J. Montero, Jennifer Powers, Salendra Singh, Paul G. Pavicic, Ivan Jurić, C. Marcela Díaz‐Montero, Jennifer S. Ko, Timothy A. Chan, Prerana Bangalore Parthasarathy
article en
2 citations

Abstract

Our findings highlight CD33<sup>+</sup> cell phenotype as a key determinant of response to chemo-immunotherapy, which can be assessed from peripheral blood. This offers a valuable tool in the context of metastatic TNBC, in which tissue sampling is often challenging.

Communications MedicineVol. 5(1)
Cleveland Clinic (US), University Hospitals Seidman Cancer Center (US)
Good health and well-being
Openalex Percentile: Top 15%
Cancer Genomics and Diagnostics
1.87
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