Outcomes and treatment patterns for stage I human epidermal growth factor receptor 2-positive breast cancer in the Surveillance, Epidemiology, and End Results database, 2010–2019

IF 5.1 2区 医学 Q1 ONCOLOGY Cancer Pub Date : 2025-01-30 DOI:10.1002/cncr.35729
Adrienne G. Waks MD, Paolo Tarantino MD, PhD, Emily L. Chen MD, Rachel A. Freedman MD, MPH, Nancy U. Lin MD, Nabihah Tayob PhD, Carlos T. Vallejo MD, Julieta Leone MD, Sara M. Tolaney MD, MPH, Jose Pablo Leone MD
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Abstract

Background

The risk of recurrence in patients with small, lymph node-negative, human epidermal growth factor receptor 2 (HER2)-positive breast cancers untreated with adjuvant chemotherapy/HER2-directed therapy is uncertain. To investigate this, the authors conducted a retrospective, population-based study of chemotherapy use and breast cancer-specific survival (BCSS) among patients with stage IA HER2-positive breast cancer.

Methods

The authors analyzed Surveillance, Epidemiology, and End Results data from patients diagnosed with stage IA HER2-positive breast cancer from 2010 to 2019. They examined the frequency of chemotherapy use by tumor size and hormone receptor (HR) status and applied multivariate logistic regression to assess the factors associated with receipt of chemotherapy. BCSS was evaluated and performed multivariable Cox regression was performed to evaluate the association between chemotherapy receipt and BCSS.

Results

Among 12,896 patients, 74.0% had HR-positive/HER2-positive breast cancer, and 26.0% had HR-negative/HER2-positive breast cancer. Adjuvant chemotherapy was received by to 58.9% of patients, with lower utilization for those who were older, Hispanic or Asian/Pacific Islander, separated/divorced/widowed, or had a lower median household income. The median follow-up was 46 months. Among the patients who had pathologic T1 (pT1) microscopic, pT1a, or pT1b tumors, the 5-year BCSS rate was 97.6%–99.6% in those who had no evidence of chemotherapy receipt in the medical record versus 98.4%–100.0% in those who did receive chemotherapy. Among patients who had pT1c tumors and had no evidence of chemotherapy receipt, the 5-year BCSS rate was 92.1% for those with HR-negative/HER2-positive breast cancer and 96.0% for those with HR-positive/HER2-positive breast cancer. Patients who had pT1c tumors and received chemotherapy had a 5-year BCSS rate of 96.7% in those with HR-negative/HER2-positive breast cancer and 98.7% in those with HR-positive/HER2-positive breast cancer.

Conclusions

In this large, population-based study of patients with stage IA HER2-positive breast cancer, patients who had tumors ≤1 cm had excellent outcomes with or without chemotherapy. Patients with pT1c tumors had a greater increase in BCSS with the receipt chemotherapy.

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2010-2019年监测、流行病学和最终结果数据库中I期人表皮生长因子受体2阳性乳腺癌的结局和治疗模式
背景:小型、淋巴结阴性、人表皮生长因子受体2 (HER2)阳性乳腺癌患者未经辅助化疗/HER2定向治疗的复发风险尚不确定。为了研究这一点,作者对IA期her2阳性乳腺癌患者的化疗使用和乳腺癌特异性生存率(BCSS)进行了一项回顾性的、基于人群的研究。方法:作者分析了2010年至2019年诊断为IA期her2阳性乳腺癌患者的监测、流行病学和最终结果数据。他们通过肿瘤大小和激素受体(HR)状态检查了化疗使用的频率,并应用多变量逻辑回归来评估与化疗接受相关的因素。评估BCSS并进行多变量Cox回归来评估化疗剂量与BCSS之间的关系。结果:12896例患者中,hr阳性/ her2阳性乳腺癌占74.0%,hr阴性/ her2阳性乳腺癌占26.0%。辅助化疗的接受率为58.9%,老年人、西班牙裔或亚洲/太平洋岛民、分居/离婚/丧偶或家庭收入中位数较低的患者的使用率较低。中位随访时间为46个月。在病理T1 (pT1)显微、pT1a或pT1b肿瘤患者中,在医疗记录中没有化疗证据的患者中,5年BCSS率为97.6%-99.6%,而在接受化疗的患者中为98.4%-100.0%。在没有接受化疗证据的pT1c肿瘤患者中,hr阴性/ her2阳性乳腺癌患者的5年BCSS率为92.1%,hr阳性/ her2阳性乳腺癌患者的5年BCSS率为96.0%。在接受化疗的pT1c肿瘤患者中,hr阴性/ her2阳性乳腺癌患者的5年BCSS率为96.7%,hr阳性/ her2阳性乳腺癌患者的5年BCSS率为98.7%。结论:在这项基于人群的IA期her2阳性乳腺癌患者的大型研究中,肿瘤≤1cm的患者无论是否接受化疗都有很好的预后。pT1c肿瘤患者的BCSS随着化疗的增加而增加。
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来源期刊
Cancer
Cancer 医学-肿瘤学
CiteScore
13.10
自引率
3.20%
发文量
480
审稿时长
2-3 weeks
期刊介绍: The CANCER site is a full-text, electronic implementation of CANCER, an Interdisciplinary International Journal of the American Cancer Society, and CANCER CYTOPATHOLOGY, a Journal of the American Cancer Society. CANCER publishes interdisciplinary oncologic information according to, but not limited to, the following disease sites and disciplines: blood/bone marrow; breast disease; endocrine disorders; epidemiology; gastrointestinal tract; genitourinary disease; gynecologic oncology; head and neck disease; hepatobiliary tract; integrated medicine; lung disease; medical oncology; neuro-oncology; pathology radiation oncology; translational research
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