| Literature DB >> 26867935 |
Lajos Pusztai1, Thomas Karn2, Anton Safonov3, Maysa M Abu-Khalaf3, Giampaolo Bianchini4.
Abstract
More than 70% of breast cancers contain lymphocytic infiltration in the stroma, and preclinical studies suggest that immunoediting and partial control of cancer progression by the local immune microenvironment operate in most breast cancers. Consistent with this hypothesis, a large number of studies demonstrated a favorable prognostic and chemotherapy response predictive role for immune infiltration in breast cancer. The evidence is particularly strong for triple-negative and HER2-positive cancers. The development of clinically effective immune checkpoint inhibitors now provides an opportunity to test the therapeutic potential of augmenting the local antitumor immune response. Several phase I clinical trials using single-agent anti-PD-1 and anti-PD-L1 antibodies demonstrated objective tumor response rates, with remarkably durable responses, in heavily pretreated, metastatic, triple-negative cancers and somewhat lower responses in estrogen receptor-positive cancers. Currently, close to 50 ongoing, or soon to open, clinical trials evaluate the role of this new treatment modality in breast cancer. Clin Cancer Res; 22(9); 2105-10. ©2016 AACR. ©2016 American Association for Cancer Research.Entities:
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Year: 2016 PMID: 26867935 PMCID: PMC9359478 DOI: 10.1158/1078-0432.CCR-15-1315
Source DB: PubMed Journal: Clin Cancer Res ISSN: 1078-0432 Impact factor: 13.801