Predictors of Nodal Pathologic Complete Response After Neoadjuvant Chemotherapy in Breast Cancer

被引:1
作者
An, Selena J. [1 ]
Thai, Christine Hong Ngoc Che [1 ]
Agala, Chris B. [1 ,2 ]
Abdou, Yara G. [3 ,4 ]
Selfridge, Julia M. [1 ,3 ]
Spanheimer, Philip M. [1 ,3 ,5 ]
机构
[1] Univ North Carolina, Dept Surg, Chapel Hill, NC 27599 USA
[2] Univ North Carolina, Gillings Sch Global Publ Hlth, Dept Epidemiol, Chapel Hill, NC USA
[3] Univ North Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
[4] Univ North Carolina Chapel Hill, Dept Med, Chapel Hill, NC USA
[5] Univ North Carolina, Dept Genet, Chapel Hill, NC 27599 USA
基金
美国国家卫生研究院;
关键词
Neoadjuvant; Nodal; Pathologic complete response; Axilla; Breast cancer; SURGERY; SURVIVAL; THERAPY; BIOPSY; IMPACT; WOMEN;
D O I
10.1245/s10434-025-17906-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Nodal pathologic complete response (npCR) after neoadjuvant treatment in patients with node-positive breast cancer (BC) avoids the morbidity of axillary dissection. In this study, we aimed to identify predictors of npCR. Patients and Methods Adult women with stage 2-3 BC and clinically positive nodes from 2011 to 2021 in the National Cancer Database who received neoadjuvant chemotherapy followed by surgery within 8 months were included. Predictors of npCR were modeled with multivariable logistic regression. Results In total, 47,483 patients were included: 18,978 (40.0%) with npCR and 28,505 (60.0%) with nodal residual disease (nRD). Median age for the npCR group was 53 years (interquartile range [IQR] 21-90 years) compared with 54 years (IQR 21-90 years, p < 0.001) in the nRD group. Triple negative breast cancer (TNBC) was the most common subtype (53.5%) in the npCR group while ER+/HER2- was the most common (46.5%) in the nRD group, p < 0.001. After adjusting for sociodemographic factors, comorbidities, tumor characteristics, and treatment, younger age (odds ratio [OR] 0.99, 95% confidence interval [CI] 0.99-0.99), ER-/HER2+ compared with TNBC (OR 1.32, 95% CI 1.21-1.44), and receipt of immunotherapy (OR 1.60, 95% CI 1.46-1.74) were associated with npCR. Black patients were less likely to have npCR overall (OR 0.90, 95% CI 0.85-0.95) with TNBC and HER2+ tumors, but more likely in ER+/HER2- tumors. Conclusions Both tumor and sociodemographic factors were associated with npCR in patients with BC. Black compared with white patients were more likely to have npCR in the ER+/HER2- subtype but less likely in the hormone receptor-negative and HER2+ subtypes. Mechanisms underlying these differences should be further investigated.
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