TY - JOUR
T1 - Immunotherapy in Breast Cancer Patients
T2 - A Focus on the Use of the Currently Available Biomarkers in Oncology
AU - Criscitiello, Carmen
AU - Guerini-Rocco, Elena
AU - Viale, Giulia
AU - Fumagalli, Caterina
AU - Sajjadi, Elham
AU - Venetis, Konstantinos
AU - Piciotti, Roberto
AU - Invernizzi, Marco
AU - Malapelle, Umberto
AU - Fusco, Nicola
N1 - Publisher Copyright:
© 2022 Bentham Science Publishers.
PY - 2022/2
Y1 - 2022/2
N2 - 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.
AB - 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.
KW - Biomarkers
KW - Breast cancer
KW - Immunotherapy
KW - Microsatellite instability
KW - Mismatch repair
KW - PD-L1
KW - TILs
KW - Tumor mutational burden
UR - http://www.scopus.com/inward/record.url?scp=85125576376&partnerID=8YFLogxK
U2 - 10.2174/1871520621666210706144112
DO - 10.2174/1871520621666210706144112
M3 - Review article
SN - 1871-5206
VL - 22
SP - 787
EP - 800
JO - Anti-Cancer Agents in Medicinal Chemistry
JF - Anti-Cancer Agents in Medicinal Chemistry
IS - 4
ER -