Department of Breast Oncology, Saitama Medical University International Medical Center, 1397-1 Yamane, Hidaka, Saitama, 350-1298, Japan.
Department of Breast Surgery, Osaka National Hospital, 2-1-14, Houenzaka, Chuo-ku Osaka-shi, Osaka, 540-0006, Japan.
Breast Cancer. 2020 Jan;27(1):85-91. doi: 10.1007/s12282-019-00997-w. Epub 2019 Jul 20.
Adding taxane to an anthracycline-based regimen improves survival in node-positive breast cancer patients, as shown by clinical trials and meta-analyses. However, no studies have analyzed the number of metastatic lymph nodes in patients with estrogen receptor (ER)-positive cancer. This study investigated whether adding a taxane to an anthracycline-based regimen improved prognosis in node-positive, ER-positive, human epidermal growth factor receptor 2 (HER2)-negative breast cancer patients in a real-world setting.
Using Japanese Breast Cancer Society registry data, we compared disease-free survival (DFS) of patients with ER-positive, HER2-negative breast cancer, excluding those receiving neoadjuvant chemotherapy, between those who received an anthracycline-based regimen followed by a taxane-based regimen (A + T) and those who received only an anthracycline-based regimen (A w/o T), stratified by lymph node status. A Cox proportional hazards model was used to evaluate DFS in both groups.
There were 4566 eligible patients with ER-positive, HER2-negative breast cancer. During the median follow-up period of 60 months, there were 481 recurrences and 149 deaths. There was no significant difference in DFS between the A + T and A w/o T groups among patients with 1-3 positive nodes, while there was a significant difference among patients with ≥ 4 positive nodes.
In patients with ER-positive, HER2-negative breast cancer, adding taxane to an anthracycline regimen did not improve DFS in patients with metastasis in 1-3 lymph nodes. We considered that the group without the addition of taxane might be present in patients with ER-positive, HER2-negative lymph node metastases.
临床试验和荟萃分析表明,在阳性淋巴结乳腺癌患者中,在蒽环类药物为基础的方案中添加紫杉烷可改善生存。然而,尚无研究分析过雌激素受体(ER)阳性癌症患者的转移性淋巴结数量。本研究旨在探讨在真实环境中,对于阳性淋巴结、ER 阳性、人表皮生长因子受体 2(HER2)阴性的乳腺癌患者,在蒽环类药物为基础的方案中添加紫杉烷是否可改善预后。
利用日本乳腺癌学会注册数据,我们比较了排除接受新辅助化疗的患者后,ER 阳性、HER2 阴性乳腺癌患者的无病生存(DFS),这些患者接受了蒽环类药物为基础的方案(A 组)加紫杉烷类药物为基础的方案(A+T 组)与仅接受蒽环类药物为基础的方案(A 组),按淋巴结状态分层。采用 Cox 比例风险模型评估两组患者的 DFS。
共有 4566 例符合条件的 ER 阳性、HER2 阴性乳腺癌患者。在中位随访 60 个月期间,有 481 例复发和 149 例死亡。在 1-3 个阳性淋巴结患者中,A+T 组与 A 组之间的 DFS 无显著差异,而在≥4 个阳性淋巴结患者中则有显著差异。
在 ER 阳性、HER2 阴性乳腺癌患者中,在蒽环类药物方案中添加紫杉烷并不能改善 1-3 个淋巴结转移患者的 DFS。我们认为,在 ER 阳性、HER2 阴性淋巴结转移的患者中,可能没有添加紫杉烷的情况。