Mansour E G, Eudey L, Tormey D C, Shatila A H, Osborne C K, Gilchrist K W, Cooper M R, Falkson G
MetroHealth Medical Center, Case Western Reserve University, Cleveland, Ohio.
J Natl Cancer Inst Monogr. 1992(11):97-104.
Postoperative women with breast cancer but without histopathological evidence of metastases to the axillary lymph nodes or clinical evidence of metastases were studied. Six hundred fifty-five "good-risk" patients who were estrogen receptor positive (ER+) with primary tumors less than 3 cm were registered for observation. Twenty-four of these patients were treated with chemotherapy. Five hundred thirty-six "poor-risk" patients who were either ER+ with primary tumors greater than or equal to 3 cm or estrogen receptor negative (ER-) with any primary tumor size were randomly assigned between chemotherapy and observation. Randomization was stratified by type of surgical procedure, number of lymph nodes examined, menopausal status, tumor size, and ER status. The chemotherapy (CMFP) consisted of six 4-week cycles of cyclophosphamide, 100 mg/m2 orally days 1-14; methotrexate, 40 mg/m2 intravenously (IV) days 1 and 8; fluorouracil, 600 mg/m2 IV days 1 and 8; and prednisone, 40 mg/m2 orally days 1-14. Treatment arms in the randomly assigned patients were balanced with respect to pretreatment characteristics. This analysis includes 445 eligible patients entered in the registration arm and 425 eligible patients entered into the randomized treatments. The median follow-up is 4.5 years in the randomly assigned cohort and 4.8 years in the registered cohort. The overall 5-year disease-free survival (DFS) among the randomly assigned patients was 83% with CMFP and 61% with observation (P less than .0001). A DFS treatment benefit was observed in premenopausal and postmenopausal patients as well as in patients with ER+ or ER- tumors. There were fewer local-regional and distant relapses among the CMFP-treated patients.(ABSTRACT TRUNCATED AT 250 WORDS)
对患有乳腺癌但无腋窝淋巴结转移组织病理学证据或转移临床证据的术后女性进行了研究。登记观察了655例“低风险”患者,这些患者雌激素受体阳性(ER+),原发肿瘤小于3厘米。其中24例患者接受了化疗。536例“高风险”患者,要么是原发肿瘤大于或等于3厘米的ER+患者,要么是任何原发肿瘤大小的雌激素受体阴性(ER-)患者,被随机分配接受化疗或观察。随机分组按手术方式、检查的淋巴结数量、绝经状态、肿瘤大小和ER状态进行分层。化疗方案(CMFP)包括六个为期4周的周期,具体为:环磷酰胺,100mg/m²,口服,第1 - 14天;甲氨蝶呤,40mg/m²,静脉注射(IV),第1天和第8天;氟尿嘧啶,600mg/m²,IV,第1天和第8天;泼尼松,40mg/m²,口服,第1 - 14天。随机分组患者的治疗组在预处理特征方面是平衡的。该分析包括登记组中的445例符合条件的患者和随机治疗组中的425例符合条件的患者。随机分组队列的中位随访时间为4.5年,登记队列的中位随访时间为4.8年。随机分组患者中,接受CMFP治疗的总体5年无病生存率(DFS)为83%,观察治疗的为61%(P<0.0001)。在绝经前和绝经后患者以及ER+或ER-肿瘤患者中均观察到DFS治疗益处。CMFP治疗的患者局部区域和远处复发较少。(摘要截断于250字)