Predictive and prognostic effect of HO-1 expression in breast cancer patients undergoing neoadjuvant chemotherapy

被引:5
作者
Tan, Qixing [1 ]
Qin, Qinghong [1 ]
Huang, Zhen [1 ]
Lian, Bin [1 ]
Mo, Qinguo [1 ]
Wei, Changyuan [1 ]
机构
[1] Guangxi Med Univ, Canc Hosp, Dept Breast Surg, 71 Hedi Rd, Nanning 530021, Guangxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Breast cancer; HO-1; Neoadjuvant chemotherapy; Biomarker; Prognosis; PATHOLOGICAL COMPLETE RESPONSE; SURGICAL ADJUVANT BREAST; OXYGENASE; EXPRESSION; HEME OXYGENASE-1; TUMOR-GROWTH; LUNG-CANCER; CELL-PROLIFERATION; POOR-PROGNOSIS; INHIBITION; METABOLISM;
D O I
10.1007/s10549-022-06565-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Heme oxygenase-1 (HO-1) has complex biological function, and is a candidate oncogene with a wide variety of deleterious functions in breast cancer. Here, we evaluated the relationship between expression of HO-1 protein with clinical response to neoadjuvant chemotherapy (NAC) in breast cancer patients. Methods We used immunohistochemistry (IHC) to determine expression of HO-1 protein from core needle biopsy before NAC, then applied univariate and multivariate analyses to understand the relationship between HO-1 with pathological complete response (pCR) outcomes. Next, Kaplan-Meier and Log-rank tests were used to compare disease-free survival (DFS) and overall survival (OS), between groups, and Cox proportional hazards regression analysis applied for prognostic evaluation. Results A total of 575 patients with locally advanced invasive breast cancer were included in the study, of which 111 (19.3%) achieved pCR after NAC. Results from multivariate analysis showed that high HO-1 expression was an independent predictor of low pCR rate (OR 0.254, 95% CI 0.026-0.643, p = 0.002). Moreover, results from survival analysis showed that high HO-1 expression was significantly associated with shorter DFS (HR 4.843, 95% CI 1.205-32.572, p = 0.026), but not with OS (HR 3.219, 95% CI 0.928-32.124, p = 0.071). Furthermore, HO-1 expression was significantly associated with lower pCR rate (OR 0.102, 95% CI 0.013-0.352), p = 0.001), poor DFS (HR 8.562, 95% CI 1.592-34.950, p = 0.009), and OS (HR 7.835, 95% CI 1.220-56.213, p = 0.023) of patients with triple-negative breast cancer (TNBC) patients. Conclusion Our results indicated that HO-1 expression is not only a biomarker for predicting pCR, but also a prognostic factor in breast cancer patients in a neoadjuvant setting, especially in TNBC subgroups.
引用
收藏
页码:393 / 403
页数:11
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