Department of Breast and Endocrine Surgery, Okayama University Hospital, 2-5-1 Shikata-cho, Kita-ku, Okayama, Japan.
Jpn J Clin Oncol. 2012 Oct;42(10):970-3. doi: 10.1093/jjco/hys120. Epub 2012 Jul 24.
This trial is being conducted to confirm the superiority, in terms of overall survival, of primary tumour resection plus systemic therapy to systemic therapy alone in patients with Stage IV breast cancer who are not refractory to primary systemic therapy. The inclusion criteria for the study are as follows: untreated patients with histologically confirmed invasive breast cancer with one or more measurable metastatic lesions diagnosed by radiological examination. All patients receive primary systemic therapy according to the estrogen receptor and human epidermal growth factor receptor type-2 status of the primary breast cancer after the first registration. After 3 months, the patients without disease progression are randomized to the primary tumour resection plus systemic therapy arm or the systemic therapy alone arm. The primary endpoint is the overall survival, and the secondary endpoints are proportion of patients without tumour progression at the metastatic sites, yearly local recurrence-free survival, proportion of local ulcer/local bleeding, yearly primary tumour resection-free survival, adverse events of chemotherapy, operative morbidity and serious adverse events. The patient recruitment was commenced in May 2011. Enrolment of 410 patients for randomization is planned over a 5 year recruitment period. We hereby report the details of the study.
本试验旨在确认对于非原发性系统治疗耐药的 IV 期乳腺癌患者,原发肿瘤切除术联合全身治疗在总生存方面优于单纯全身治疗。研究的纳入标准如下:未经治疗的组织学证实的浸润性乳腺癌患者,具有一个或多个可测量的转移病灶,通过影像学检查诊断。所有患者在首次登记后根据原发性乳腺癌的雌激素受体和人表皮生长因子受体 2 状态接受原发性全身治疗。3 个月后,无疾病进展的患者随机分配至原发肿瘤切除术联合全身治疗组或单纯全身治疗组。主要终点是总生存,次要终点是转移部位无肿瘤进展的患者比例、每年局部无复发生存率、局部溃疡/局部出血比例、每年原发性肿瘤切除术无复发生存率、化疗不良事件、手术发病率和严重不良事件。患者招募于 2011 年 5 月开始。计划在 5 年的招募期内招募 410 名患者进行随机分组。现将研究详情报告如下。