期刊
INTERNATIONAL JOURNAL OF ONCOLOGY
卷 57, 期 6, 页码 1245-1261出版社
SPANDIDOS PUBL LTD
DOI: 10.3892/ijo.2020.5135
关键词
triple-negative breast cancer; clinical studies; immunotherapy; DNA-damage response; targeted therapy; therapeutic strategy
类别
Triple-negative breast cancer (TNBC) accounts for 10-15% of all breast cancer cases. TNBCs lack estrogen and progesterone receptors and express low levels of HER2, and therefore do not respond to hormonal or anti-HER2 therapies. TNBC is a particularly aggressive form of breast cancer that generally displays poorer prognosis compared to other breast cancer subtypes. TNBC is chemotherapy sensitive, and this treatment remains the standard of care despite its limited benefit. Recent advances with novel agents have been made for specific subgroups with PD-L1(+) tumors or germline Brca-mutated tumors. However, only a fraction of these patients responds to immune checkpoint or PARP inhibitors and even those who do respond often develop resistance and relapse. Various new agents and combination strategies have been explored to further understand molecular and immunological aspects of TNBC. In this review, we discuss clinical trials in the management of TNBC as well as perspectives for potential future treatments.
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