Morrison J M, Howell A, Kelly K A, Grieve R J, Monypenny I J, Walker R A, Waterhouse J A
Selly Oak Hospital, Birmingham, UK.
Br J Cancer. 1989 Dec;60(6):911-8. doi: 10.1038/bjc.1989.389.
The aim of this study was to test the effectiveness of a regimen of combination chemotherapy known to be active in advanced breast cancer when given as an adjuvant treatment after mastectomy. A total of 569 patients with cancer of the breast and involvement of axillary lymph nodes were randomised, after simple mastectomy with axillary sampling, to receive either no adjuvant treatment or intravenous adriamycin 50 mg, vincristine 1 mg, cyclophosphamide 250 mg, methotrexate 150 mg and fluorouracil 250 mg (AVCMF) every 21 days for eight cycles. Randomisation was stratified according to menopausal status and tumour size. Treatment was started within 14 days of surgery in 94% of patients. Eighty-eight per cent of patients received at least seven cycles of chemotherapy with no dose reduction. The median relapse-free survival was prolonged by 14 months in patients treated with AVCMF (chi2 1 = 11.7; P = 0.0006). In the premenopausal group this period was 17 months (chi2 1 = 8.8; P = 0.003) compared with 8 months in the post-menopausal group (chi2 1 = 3.3; P = 0.07). Neither overall survival nor survival in these subgroups was significantly influenced by treatment.
本研究的目的是测试一种联合化疗方案的有效性,该方案在晚期乳腺癌中显示出活性,在乳房切除术后作为辅助治疗使用。共有569例患有乳腺癌且腋窝淋巴结受累的患者,在进行单纯乳房切除并取腋窝样本后,被随机分配接受无辅助治疗或静脉注射阿霉素50毫克、长春新碱1毫克、环磷酰胺250毫克、甲氨蝶呤150毫克和氟尿嘧啶250毫克(AVCMF),每21天一个周期,共八个周期。随机分组根据绝经状态和肿瘤大小进行分层。94%的患者在手术后14天内开始治疗。88%的患者接受了至少七个周期的化疗且未减少剂量。接受AVCMF治疗的患者中位无复发生存期延长了14个月(卡方检验1=11.7;P=0.0006)。在绝经前组,这一时期为17个月(卡方检验1=8.8;P=0.003),而绝经后组为8个月(卡方检验1=3.3;P=0.07)。治疗对总生存期或这些亚组的生存期均无显著影响。