Interactive effects of molecular subtypes with tumor size and extracranial metastatic pattern on risk of brain metastasis in breast cancer patients: A population-based study

被引:1
|
作者
Shen, Bo [1 ,2 ]
Li, Jieqing [2 ]
Yang, Mei [2 ]
Liu, Kangkang [3 ]
Zhang, Junsheng [4 ]
Li, Weiping [5 ]
Zhang, Yi [2 ]
Wang, Kun [1 ,2 ]
机构
[1] Shantou Univ, Med Coll, Shantou, Peoples R China
[2] Guangdong Acad Med Sci, Guangdong Prov Peoples Hosp, Canc Ctr, Dept Breast Canc, 123 Huifu West Rd, Guangzhou 510080, Peoples R China
[3] Sun Yat Sen Univ, Affiliated Hosp 8, Dept Res Ctr Med, Shenzhen, Peoples R China
[4] Sun Yat Sen Univ, Collaborat In Novat Ctr Canc Med, State Key Lab Oncol South China, Canc Ctr, Guangzhou, Peoples R China
[5] Guangdong Pharmaceut Univ, Affiliated Hosp 1, Sch Clin Med, Guangzhou, Peoples R China
来源
CANCER MEDICINE | 2023年 / 12卷 / 06期
基金
中国国家自然科学基金;
关键词
brain metastasis; breast cancer; extracranial metastasis; interaction analysis; molecular subtype; tumor size; CHEMOTHERAPY; FEATURES; DISEASE; STAGE;
D O I
10.1002/cam4.5425
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Early detection of brain metastasis (BM) is essential for prognostic improvement in breast cancer (BC) patients. The aim was to identify predictors of BCBM in different molecular subtypes on a population-based level. Methods The Surveillance, Epidemiology, and End Results database was used to select BC patients diagnosed from 2010 to 2018. We evaluated the incidence and risk factors of BCBM and tested the interaction effects between molecular subtypes and other risk factors. Results Among the 527,525 selected patients, molecular subtypes significantly interacted with T stage and extracranial metastasis (ECM) patterns on the risk of BM in the whole BC population (interaction p = 0.002, <0.001, respectively) and after excluding patients with unknown states of key factors. BM development was independent of the T stage only in HR-/HER2- patients (trend p = 0.126). We selected BC patients with single-organ ECM and found a significant interaction between molecular subtypes and ECM patterns (interaction p = 0.013). The impact of ECM patterns on the risk of BM was limited to HR-/HER2- patients (trend p < 0.001), for whom using bone metastasis as a reference, lung metastasis increased the risk of BM (OR = 1.936, 95% CI: 1.300-2.882, p = 0.001). Conclusion T stage and ECM patterns had different associations with BM in different molecular subtypes. HR-/HER2- BC had distinct features on BM development, manifested as a lack of tumor size effect and is associated with lung metastasis. Close surveillance for BM should be considered for HR-/HER2- BC patients.
引用
收藏
页码:6547 / 6557
页数:11
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