4.6 Article

Case Report: A Case Study Documenting the Activity of Atezolizumab in a PD-L1-Negative Triple-Negative Breast Cancer

Journal

FRONTIERS IN ONCOLOGY
Volume 11, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fonc.2021.710596

Keywords

immunotherapy; breast cancer; biomarkers; ctDNA; case report

Categories

Funding

  1. Instituto de Salud Carlos III [PI19/01846]
  2. Breast Cancer Now [2018NOVPCC1294]
  3. Breast Cancer Research Foundation-AACR Career Development Awards for Translational Breast Cancer Research [19-20-26-PRAT]
  4. Fundacio La Marato [TV3 201935-30]
  5. European Union [H2020-SC1-BHC-2018-2020]
  6. Asociacion de Cancer de Mama Metastasico [CMM_CHIARAG19_001]
  7. Pas a Pas
  8. Save the Mama
  9. Fundacion Cientifica Asociacion Espanola Contra el Cancer [AECC_Postdoctoral17_1062, INVES19056SANS]
  10. FERO-ghd 2020 breast cancer award
  11. Generalitat de Catalunya Peris PhD4MD 2019 [SLT008/18/00122]

Ask authors/readers for more resources

A case study demonstrated significant response to atezolizumab in a PD-L1-negative TNBC patient, potentially due to factors such as high TMB, presence of APOBEC genetic signatures, tumor inflammation signature, and HER2-enriched subtype. Additional translational studies are needed to identify biomarkers for response to immune checkpoint inhibitors beyond PD-L1 expression in TNBC patients.
The immune checkpoint inhibitor atezolizumab is approved for PD-L1-positive triple-negative breast cancer (TNBC). However, no activity of atezolizumab in PD-L1-negative TNBC has been reported to date. Here, we present the case study of a woman with TNBC with low tumor infiltrating lymphocytes and PD-L1-negative disease, which achieved a significant response to atezolizumab monotherapy and durable response after the combination of atezolizumab and nab-paclitaxel. The comprehensive genomic analysis that we performed in her tumor and plasma samples revealed high tumor mutational burden (TMB), presence of the APOBEC genetic signatures, high expression of the tumor inflammation signature, and a HER2-enriched subtype by the PAM50 assay. Some of these biomarkers have been shown to independently predict response to immunotherapy in other tumors and may explain the durable response in our patient. Our work warrants further translational studies to identify biomarkers of response to immune checkpoint inhibitors in TNBC beyond PD-L1 expression and to better select patients that will benefit from immunotherapy.

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