Departments of Breast and Endocrine Surgery, Tokai University School of Medicine, Kanagawa, 143 Shimokasuya, Isehara, Kanagawa, 259-1193, Japan.
Department of Breast and Medical Oncology, National Cancer Center, Tokyo, Japan.
Breast Cancer Res Treat. 2018 Jan;167(1):81-87. doi: 10.1007/s10549-017-4489-9. Epub 2017 Sep 11.
Though advanced and metastatic epidermal growth factor receptor 2 (HER2)-positive disease is not curable, a small proportion of patients with HER2-positive metastatic breast cancer remain in prolonged complete remission with anti-HER2 treatment. We hypothesized that some cases of HER2-positive metastatic breast cancer may be curable. In this large, multicenter retrospective study, we aimed to assess the long-term outcomes for patients with a durable response to trastuzumab.
We retrospectively evaluated the data of patients diagnosed with HER2-positive metastatic breast cancer who received trastuzumab for more than 2 years as the first-line treatment. Patients diagnosed between April 1, 2001 and December 31, 2014 at 19 institutions in Japan were included in the analysis. From 124 potential subjects, 16 were excluded and 108 were evaluated.
The median follow-up length was 7.7 years. Disease progression occurred in 44/108 (40.7%) patients and 13/108 (12%) patients died. The median progression-free survival was 11.2 years, and as more than 80% of patients were alive 10 years after metastatic breast cancer diagnosis. Of the 108 patients, 57 achieved a clinical complete response. Trastuzumab therapy was interrupted for 27 (47.4%) of these patients (based on the doctor's recommendation for 19 patients, owing to adverse events for 4 patients, owing to unknown reasons for 3 patients, and at the request of 1 patient). Disease progression occurred in 4 of the 27 patients after the interruption of trastuzumab treatment. The median duration of trastuzumab therapy for all 27 patients was 5.1 years (0.9-9.3 years).
We found that some patients showed no evidence of disease after the interruption of trastuzumab therapy. Discontinuation of maintenance trastuzumab in this patient population after a limited time should be explored cautiously while awaiting a global collaborative effort for a randomized trial.
尽管晚期和转移性表皮生长因子受体 2(HER2)阳性疾病无法治愈,但仍有一小部分 HER2 阳性转移性乳腺癌患者在接受抗 HER2 治疗后持续完全缓解。我们假设,一些 HER2 阳性转移性乳腺癌病例可能是可治愈的。在这项大型、多中心回顾性研究中,我们旨在评估对曲妥珠单抗有持久反应的患者的长期结局。
我们回顾性评估了在 19 家日本机构接受曲妥珠单抗治疗超过 2 年作为一线治疗的 HER2 阳性转移性乳腺癌患者的数据。该研究纳入了 2001 年 4 月 1 日至 2014 年 12 月 31 日期间诊断的患者。在 124 名潜在受试者中,有 16 名被排除在外,108 名被评估。
中位随访时间为 7.7 年。44/108(40.7%)例患者出现疾病进展,13/108(12%)例患者死亡。中位无进展生存期为 11.2 年,超过 80%的患者在转移性乳腺癌诊断后 10 年仍存活。在 108 例患者中,57 例达到临床完全缓解。这些患者中有 27 例(47.4%)中断了曲妥珠单抗治疗(根据医生建议中断治疗 19 例,因不良事件中断治疗 4 例,因未知原因中断治疗 3 例,1 例患者要求中断治疗)。曲妥珠单抗治疗中断后,有 4 例患者出现疾病进展。27 例患者的曲妥珠单抗治疗中位时间为 5.1 年(0.9-9.3 年)。
我们发现一些患者在曲妥珠单抗治疗中断后没有疾病证据。在等待全球合作进行随机试验的同时,应谨慎探索在有限时间后在这部分患者人群中停止维持性曲妥珠单抗治疗。