三阴性乳腺癌
医学
乳腺癌
免疫疗法
肿瘤科
免疫检查点
PARP抑制剂
肿瘤微环境
化疗
内科学
靶向治疗
癌症
癌症研究
聚ADP核糖聚合酶
生物
基因
聚合酶
生物化学
作者
Julia Dixon-Douglas,Sibylle Loibl,Carsten Denkert,Melinda L. Telli,Sherene Loi
出处
期刊:American Society of Clinical Oncology educational book
[American Society of Clinical Oncology]
日期:2022-07-01
卷期号: (42): 47-59
被引量:9
摘要
Triple-negative breast cancer (TNBC) is the most aggressive histologic subtype of breast cancer for which, until recently, treatment options have been limited to chemotherapy. In recent years, an improved understanding of the importance of tumor-infiltrating lymphocytes and the tumor microenvironment in TNBC has led to investigation of immune checkpoint inhibitors for treatment. There is now evidence from several randomized controlled trials that supports the addition of immune checkpoint inhibitors to first-line treatment of advanced TNBC and to neoadjuvant chemotherapy for stage II-III TNBC. In parallel, the PARP inhibitors have emerged as a targeted therapy option for patients with HER2-negative breast cancer harboring mutations in BRCA1, BRCA2, and PALB2. Here, we review the recent clinical trials that inform the integration of immune checkpoint inhibitors into treatments for TNBC and discuss ongoing challenges-including patient selection, management of resistance to post-checkpoint inhibitor therapy, and combining immunotherapy with targeted therapies, including PARP inhibitors.
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