Department of Breast Surgery, Guangxi Medical University Cancer Hospital, 71 Hedi Road, Nanning, 530021, Guangxi, People's Republic of China.
Breast Cancer Res Treat. 2022 Jun;193(2):393-403. doi: 10.1007/s10549-022-06565-9. Epub 2022 Mar 18.
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.
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.
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.
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.
血红素加氧酶-1(HO-1)具有复杂的生物学功能,是一种候选癌基因,在乳腺癌中具有多种有害功能。在这里,我们评估了 HO-1 蛋白表达与乳腺癌患者新辅助化疗(NAC)临床反应之间的关系。
我们使用免疫组织化学(IHC)方法测定 NAC 前核心针活检中 HO-1 蛋白的表达,然后应用单因素和多因素分析来了解 HO-1 与病理完全缓解(pCR)结果之间的关系。接下来,使用 Kaplan-Meier 和 Log-rank 检验比较无病生存(DFS)和总生存(OS),组间差异,并应用 Cox 比例风险回归分析进行预后评估。
共纳入 575 例局部晚期浸润性乳腺癌患者,其中 111 例(19.3%)NAC 后达到 pCR。多因素分析结果表明,高 HO-1 表达是 pCR 率低的独立预测因子(OR 0.254,95%CI 0.026-0.643,p=0.002)。此外,生存分析结果表明,高 HO-1 表达与较短的 DFS 显著相关(HR 4.843,95%CI 1.205-32.572,p=0.026),但与 OS 无关(HR 3.219,95%CI 0.928-32.124,p=0.071)。此外,HO-1 表达与较低的 pCR 率显著相关(OR 0.102,95%CI 0.013-0.352,p=0.001),DFS 较差(HR 8.562,95%CI 1.592-34.950,p=0.009)和 OS(HR 7.835,95%CI 1.220-56.213,p=0.023)与三阴性乳腺癌(TNBC)患者相关。
我们的研究结果表明,HO-1 表达不仅是预测 pCR 的生物标志物,而且是新辅助治疗中乳腺癌患者的预后因素,特别是在 TNBC 亚组中。