Monitoring of Triple Negative Breast Cancer After Neoadjuvant Chemotherapy

被引:4
|
作者
Aldrich, Jeffrey [1 ]
Canning, Madison [2 ]
Bhave, Manali [1 ,3 ]
机构
[1] Emory Univ, Winship Canc Inst, Dept Hematol & Med Oncol, Atlanta, GA USA
[2] Emory Univ, Emory Sch Med, Dept Med, Atlanta, GA USA
[3] Emory Univ, Winship Canc Inst, 1365 Clifton Rd NE,Bldg C,Suite 4000, Atlanta, GA 30322 USA
关键词
Clinical trials; ctDNA; Immunotherapy; Neoadjuvant therapy; TNBC;
D O I
10.1016/j.clbc.2023.08.001
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Triple negative breast cancer (TNBC) is an aggressive disease with a poor prognosis that disproportionately affects young women and Afr ican Amer icans, and represents a major unmet need in the field. TNBCs display a more aggressive growth pattern with an increased risk of advanced disease and high recurrence risk in patients with early stage TNBC. The addition of immunotherapy to chemotherapy for the treatment of patients with early stage TNBC in the (neo) adjuvant setting per the pivotal KEYNOTE 522 significantly improved pCR rates. Despite this advancement, however, approximately 35% of patients had residual disease at the time of surgery and reduced event free survival. Further techniques to assess for molecular residual disease after completion of neoadjuvant chemotherapy (NAC) may allow us to identify patients at high risk of relapse who may benefit from salvage adjuvant systemic therapy, while also potentially de-escalating treatment in those achieving a molecular complete response.
引用
收藏
页码:832 / 834
页数:3
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