The landscape of systemic therapy for early stage triple-negative breast cancer

被引:6
|
作者
Lu, Jin-Yu [1 ]
Soto, Alvaro Alvarez [1 ]
Anampa, Jesus D. [1 ]
机构
[1] Montefiore Med Ctr, Albert Einstein Canc Ctr, Albert Einstein Coll Med, Dept Oncol,Sect Breast Med Oncol, Bronx, NY 10461 USA
关键词
Triple-negative breast cancer; systemic adjuvant therapy; immune checkpoint inhibitor; targeted therapy; chemotherapy; pathologic complete response; STANDARD NEOADJUVANT CHEMOTHERAPY; SURGICAL ADJUVANT BREAST; PHASE-III TRIAL; FOLLOW-UP; COMBINATION CHEMOTHERAPY; CAPECITABINE MAINTENANCE; DOSE-DENSE; CARBOPLATIN; DOXORUBICIN; SURVIVAL;
D O I
10.1080/14656566.2022.2095902
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Triple-negative breast cancer (TNBC) is the most aggressive subtype of breast cancer with higher risk of disease recurrence and mortality than other breast cancer subtypes. Historically, chemotherapy has been the primary systemic treatment for early stage TNBC. Recent developments in immune checkpoint inhibitors (ICIs) and novel therapeutic agents have transformed the treatment of TNBC. Areas covered: This review provides a comprehensive overview of the current evidence on treatment of early stage TNBC. We highlight the incorporation of ICIs and other targeted therapies in (neo) adjuvant treatment and the ongoing development of novel therapeutic agents. Expert opinion: The landscape of early TNBC treatment is rapidly evolving, which has given rise to the introduction of ICIs and PARP inhibitors into the systemic therapy. Despite modest improvement in the pathologic complete response (pCR) rate, ICI plus chemotherapy significantly improves long-term outcomes and is now used in (neo)adjuvant treatment of patients with TNBC and high risk for disease recurrence. Capecitabine remains the standard adjuvant treatment for residual disease, with olaparib being an option for patients with germline BRCA1/2 mutations. Early detection of minimal residual disease may identify patients requiring additional therapy to prevent recurrence.
引用
收藏
页码:1291 / 1303
页数:13
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