Cohen Lauren N, Rogers Christine C, Lloren Jan Irene C, Kamaraju Sailaja, Chaudhary Lubna N, Huang Chiang-Ching, Cobb Adrienne N, Singh Puneet, Kong Amanda L, Teshome Mediget, Cortina Chandler S
Division of Surgical Oncology, Department of Surgery, Medical College of Wisconsin, 8701 Watertown Plank Rd., Milwaukee, WI, 53226, USA.
Zibler School of Public Health, University of Wisconsin at Milwaukee, Milwaukee, WI, USA.
Breast Cancer Res Treat. 2025 Jun 3. doi: 10.1007/s10549-025-07750-2.
Neoadjuvant systemic therapy (NST) for HER2 + breast cancer (HER2 + BC) has historically been used to downstage disease to facilitate surgical de-escalation; however, in 2019, the KATHERINE trial identified a survival benefit to adjuvant T-DM1 for those with residual disease after NST. We aimed to determine national rates of NST for patients with cT1-2 N0 M0 HER2 + BC and identify factors associated with receipt of NST vs upfront surgery with adjuvant systemic therapy (US-AST).
A retrospective cohort study of women with cT1-2 N0 M0 HER2 + BC was performed using the National Cancer Database from 2016-2021. ANOVA, Kruskal-Wallis, Chi-square, Fisher's Exact tests, and a multivariable logistic regression analysis were used.
54,449 patients met inclusion: 30,546 (56.1%) received US-AST and 19,562 (35.9%) received NST. NST utilization increased from 31.1% in 2016-17 to 43.3% in 2020-21. On regression analysis, women diagnosed in 2020-21 were more likely to receive NST (OR 1.9, 95% CI 1.8-2.0). Populations less likely to receive NST included NH-Black women (OR 0.87, 95% CI 0.8-0.95), age ≥ 70 (OR 0.7, 95% CI 0.6-0.8), increasing comorbidities (OR 0.7, 95% CI 0.5-0.9), and Medicare insurance (OR 0.8, 95% CI 0.7-0.8). Patients with cT2 disease were more likely to receive NST vs those with cT1 disease (p < 0.001).
From 2016-2021, national rates of NST for patients with cT1-2 N0 HER2 + BC significantly increased. Race/ethnicity and insurance type were associated with receipt of NST underscoring ongoing disparities in care. Future studies are needed to determine the impact of the disparate rates of NST utilization on oncologic outcomes, given the survival benefit with adjuvant T-DM1 in those with residual disease after NST.
人表皮生长因子受体2阳性乳腺癌(HER2+BC)的新辅助全身治疗(NST)在历史上一直用于降低疾病分期,以促进手术降级;然而,2019年,KATHERINE试验发现,对于新辅助全身治疗后仍有残留疾病的患者,辅助性曲妥珠单抗-美坦新偶联物(T-DM1)具有生存获益。我们旨在确定cT1-2 N0 M0 HER2+BC患者的全国新辅助全身治疗率,并确定与接受新辅助全身治疗或 upfront手术联合辅助全身治疗(US-AST)相关的因素。
使用2016年至2021年的国家癌症数据库对cT1-2 N0 M0 HER2+BC女性患者进行回顾性队列研究。采用方差分析、Kruskal-Wallis检验、卡方检验、Fisher精确检验和多变量逻辑回归分析。
54449例患者符合纳入标准:30546例(56.1%)接受了upfront手术联合辅助全身治疗(US-AST),19562例(35.9%)接受了新辅助全身治疗(NST)。新辅助全身治疗的使用率从2016-2017年的31.1%增至2020-2021年的43.3%。回归分析显示,2020-2021年诊断的女性更有可能接受新辅助全身治疗(比值比[OR]1.9,95%置信区间[CI]1.8-2.0)。不太可能接受新辅助全身治疗的人群包括非裔美国黑人女性(OR 0.87,95%CI 0.8-0.95)、年龄≥70岁(OR 0.7,95%CI 0.6-0.8)、合并症增加(OR 0.7,95%CI 0.5-0.9)以及参加医疗保险(OR 0.8,95%CI 0.7-0.8)。与cT1期疾病患者相比,cT2期疾病患者更有可能接受新辅助全身治疗(p<0.001)。
2016年至2021年,cT1-2 N0 HER2+BC患者的全国新辅助全身治疗率显著增加。种族/民族和保险类型与接受新辅助全身治疗相关,这突出了目前在医疗护理方面存在的差异。鉴于新辅助全身治疗后仍有残留疾病的患者使用辅助性曲妥珠单抗-美坦新偶联物(T-DM1)具有生存获益,未来需要开展研究以确定新辅助全身治疗使用率的差异对肿瘤学结局的影响。