Department of Breast Surgery, Hiroshima University Hospital, Hiroshima, Japan.
BMC Cancer. 2011 Mar 31;11:118. doi: 10.1186/1471-2407-11-118.
It is unclear whether individualized treatments based on biological factors have improved the prognosis of recurrent breast cancer. The purpose of this study is to evaluate the survival improvement of patients with recurrent breast cancer after the introduction of third generation aromatase inhibitors (AIs) and trastuzumab.
A total of 407 patients who received first diagnosis of recurrent breast cancer and treatment at National Kyushu Cancer Center between 1992 and 2008 were retrospectively evaluated. As AIs and trastuzumab were approved for clinical use in Japan in 2001, the patients were divided into two time cohorts depending on whether the cancer recurred before or after 2001. Cohort A: 170 patients who were diagnosed between 1992 and 2000. Cohort B: 237 patients who were diagnosed between 2001 and 2008. Tumor characteristics, treatments, and outcome were compared.
Fourteen percent of cohort A and 76% of cohort B received AIs and/or trastuzumab (P < 0.001). The median overall survival (OS) times after breast cancer recurrence were 1.7 years and 4.2 years for these respective cohorts (P < 0.001). Both the time period and treatment of AIs and/or trastuzumab for recurrent disease were significant prognostic factors in multivariate analysis (cohort B vs. cohort A: HR = 0.70, P = 0.01; AIs and/or trastuzumab for recurrent disease: yes vs. no: HR = 0.46, P < 0.001). When patients were categorized into 4 subgroups by the expression of hormone receptor (HR) and HER-2 status, the median OS times of the HR-positive/HER-2-negative, HR-positive/HER-2-positive, HR-negative/HER-2-positive, and HR-negative/HER-2-negative subtypes were 2.2, 2.4, 1.6, and 1.0 years in cohort A and 4.5, 5.1, 5.0, and 1.4 years in cohort B.
The prognosis of patients with recurrent breast cancer was improved over time following the introduction of AIs and trastuzumab and the survival improvement was apparent in HR- and/or HER-2-positive tumors.
基于生物学因素的个体化治疗是否改善了复发性乳腺癌的预后尚不清楚。本研究旨在评估第三代芳香酶抑制剂(AIs)和曲妥珠单抗引入后复发性乳腺癌患者的生存改善情况。
回顾性评估了 1992 年至 2008 年在日本九州国立癌症中心首次诊断为复发性乳腺癌并接受治疗的 407 例患者。由于 AIs 和曲妥珠单抗于 2001 年在日本获准临床使用,因此根据癌症复发是在 2001 年之前还是之后,将患者分为两个时间队列。队列 A:170 例患者于 1992 年至 2000 年确诊。队列 B:237 例患者于 2001 年至 2008 年确诊。比较肿瘤特征、治疗和结局。
队列 A 中有 14%,而队列 B 中有 76%的患者接受了 AIs 和/或曲妥珠单抗(P<0.001)。复发性乳腺癌后中位总生存期(OS)时间分别为 1.7 年和 4.2 年(P<0.001)。多因素分析显示,时间和复发性疾病中 AIs 和/或曲妥珠单抗的治疗均为显著的预后因素(队列 B 与队列 A:HR=0.70,P=0.01;复发性疾病中 AIs 和/或曲妥珠单抗:是 vs. 否:HR=0.46,P<0.001)。当根据激素受体(HR)和 HER-2 状态将患者分为 4 个亚组时,HR 阳性/HER-2 阴性、HR 阳性/HER-2 阳性、HR 阴性/HER-2 阳性和 HR 阴性/HER-2 阴性亚型的中位 OS 时间分别为队列 A 中的 2.2、2.4、1.6 和 1.0 年,队列 B 中的 4.5、5.1、5.0 和 1.4 年。
随着 AIs 和曲妥珠单抗的引入,复发性乳腺癌患者的预后随时间改善,在 HR-和/或 HER-2 阳性肿瘤中生存改善更为明显。