Rivkin S E, Green S, Metch B, Cruz A B, Abeloff M D, Jewell W R, Costanzi J J, Farrar W B, Minton J P, Osborne C K
Puget Sound Oncology Consortium, Seattle, WA.
J Clin Oncol. 1994 Oct;12(10):2078-85. doi: 10.1200/JCO.1994.12.10.2078.
To compare chemohormonal therapy, chemotherapy alone, and hormonal therapy alone in postmenopausal patients with estrogen receptor (ER)-positive operable breast cancer and positive axillary nodes with respect to survival and disease-free survival (DFS).
Eight hundred ninety-two postmenopausal women with ER-positive, node-positive breast cancer were enrolled by the Southwest Oncology Group (SWOG) from July 1979 to March 1989 and 74 by the Eastern Cooperative Oncology Group (ECOG) between June 1987 and March 1989. Patients were stratified according to number of involved nodes and type of primary surgery and randomized to receive the following: (1) tamoxifen 10 mg twice daily by mouth for 1 year; (2) cyclophosphamide 60 mg/m2/d by mouth for 1 year, methotrexate 15 mg/m2 intravenously (IV) weekly for 1 year, fluorouracil (5-FU) 400 mg/m2 IV weekly for 1 year, vincristine .625 mg/m2 IV weekly for the first 10 weeks, and prednisone during weeks 1 to 10 with doses decreasing from 30 mg/m2 to 2.5 mg/m2 (CMFVP); or (3) the combination of tamoxifen and CMFVP.
The median follow-up duration is 6.5 years, with a maximum of 12.8 years. Treatment arms are not significantly different with respect to either survival or DFS (log-rank, 2 df, P = .82 and .23, respectively). The 5-year survival rate is 77% for the tamoxifen arm, 78% for CMFVP, and 75% for the combination. No significant differences were observed in node or receptor level subsets. Severe or worse toxicity was experienced by 56% of patients on CMFVP and 61% on CMFVP plus tamoxifen, compared with 5% on tamoxifen alone.
CMFVP chemotherapy, either alone or in combination with tamoxifen, has not been shown to be superior to tamoxifen alone in the treatment of postmenopausal women with node-positive, ER-positive, operable breast cancer.
比较化学激素疗法、单纯化疗和单纯激素疗法在绝经后雌激素受体(ER)阳性可手术乳腺癌且腋窝淋巴结阳性患者中的生存率和无病生存率(DFS)。
1979年7月至1989年3月,西南肿瘤协作组(SWOG)招募了892例绝经后ER阳性、淋巴结阳性乳腺癌患者,1987年6月至1989年3月,东部肿瘤协作组(ECOG)招募了74例。患者根据受累淋巴结数量和原发手术类型进行分层,随机接受以下治疗:(1)他莫昔芬10毫克,每日口服两次,共1年;(2)环磷酰胺60毫克/平方米/天,口服1年,甲氨蝶呤15毫克/平方米,静脉注射(IV),每周1次,共1年,氟尿嘧啶(5-FU)400毫克/平方米,静脉注射,每周1次,共1年,长春新碱0.625毫克/平方米,静脉注射,每周1次,共10周,第1至10周使用泼尼松,剂量从30毫克/平方米降至2.5毫克/平方米(CMFVP);或(3)他莫昔芬与CMFVP联合使用。
中位随访时间为6.5年,最长为12.8年。各治疗组在生存率或DFS方面无显著差异(对数秩检验,2自由度,P分别为0.82和0.23)。他莫昔芬组的5年生存率为77%,CMFVP组为78%,联合组为75%。在淋巴结或受体水平亚组中未观察到显著差异。CMFVP组56%的患者和CMFVP加他莫昔芬组61%的患者经历了严重或更严重的毒性反应,而单纯他莫昔芬组为5%。
在治疗绝经后淋巴结阳性、ER阳性、可手术乳腺癌患者中,CMFVP化疗单独或与他莫昔芬联合使用并未显示优于单纯他莫昔芬。