| Literature DB >> 34229592 |
Carmen Criscitiello1,2, Elena Guerini-Rocco1,3, Giulia Viale4, Caterina Fumagalli3, Elham Sajjadi1,3, Konstantinos Venetis1,3, Roberto Piciotti1,3, Marco Invernizzi5, Umberto Malapelle6, Nicola Fusco1,3.
Abstract
Immune Checkpoint Inhibitors (ICIs) have remarkably modified the way solid tumors are managed, including breast cancer. Unfortunately, only a relatively small number of breast cancer patients significantly respond to these treatments. To maximize the immunotherapy benefit in breast cancer, several efforts are currently being put forward for the identification of i) the best therapeutic strategy (i.e. ICI monotherapy or in association with chemotherapy, radiotherapy, or other drugs); ii) optimal timing for administration (e.g. early/advanced stage of disease; adjuvant/ neoadjuvant setting); iii) most effective and reliable predictive biomarkers of response (e.g. tumor-infiltrating lymphocytes, programmed death-ligand 1, microsatellite instability associated with mismatch repair deficiency, and tumor mutational burden). In this article, we review the impacts and gaps in the characterization of immune-related biomarkers raised by clinical and translational research studies with immunotherapy treatments. Particular emphasis has been put on the documented evidence of significant clinical benefits of ICI in different randomized clinical trials, along with preanalytical and analytical issues in predictive biomarkers pathological assessment. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.Entities:
Keywords: Breast cancer; PD-L1; TILs; biomarkers; immunotherapy; microsatellite instability; mismatch repair; tumor mutational burden
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Year: 2022 PMID: 34229592 DOI: 10.2174/1871520621666210706144112
Source DB: PubMed Journal: Anticancer Agents Med Chem ISSN: 1871-5206 Impact factor: 2.505