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乳腺癌辅助治疗:西南肿瘤协作组研究

Adjuvant therapy of breast cancer: Southwest Oncology Group studies.

作者信息

Osborne C K, Rivkin S E, McDivitt R W, Green S, Stephens R L, Costanzi J J, O'Bryan R

出版信息

NCI Monogr. 1986(1):71-4.

PMID:3534592
Abstract

The Southwest Oncology Group has conducted a series of randomized studies of adjuvant therapy in patients with primary breast cancer and positive axillary nodes. The first study, during which combined chemotherapy with cyclophosphamide, methotrexate, 5-fluorouracil, vincristine, and prednisone (CMFVP) administered for 1 year was compared with single agent therapy with melphalan (L-PAM) for 2 years, was activated in 1975 and closed in 1978. Of the 366 patients who were eligible, 191 received L-PAM and 175 were given CMFVP. The 2 groups were comparable with regard to known prognostic factors. At a median follow-up of 8 years, CMFVP continues to be superior to L-PAM in disease-free (P = .005) and overall survival (P = .01). Thirty-five percent of patients on CMFVP have died compared with 46% on L-PAM. The greatest survival benefit is apparent in premenopausal women and women with 4 or more positive axillary nodes. Acute toxicity was more frequent with CMFVP than with L-PAM, but it was acceptable and reversible with both regimens. Long-term toxicity was limited to myeloproliferative disease in 2 patients on L-PAM and 1 on CMFVP. The second-generation series of studies, activated in 1979, were designed according to nodal status, estrogen receptor (ER) status, and menopausal status. We randomized ER-negative, node-negative patients to 6 months of combination chemotherapy or to no treatment. Because of slow accrual, the study was closed and patients are now being entered onto a similar intergroup study with the Eastern Cooperative Oncology Group. We randomized ER-negative, node-positive patients to either 1 or 2 years of CMFVP.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

西南肿瘤协作组开展了一系列针对原发性乳腺癌伴腋窝淋巴结阳性患者的辅助治疗随机研究。第一项研究于1975年启动,1978年结束,该研究比较了为期1年的环磷酰胺、甲氨蝶呤、5-氟尿嘧啶、长春新碱和泼尼松联合化疗(CMFVP)与为期2年的美法仑单药治疗(L-PAM)。在366例符合条件的患者中,191例接受L-PAM治疗,175例接受CMFVP治疗。两组在已知预后因素方面具有可比性。中位随访8年时,CMFVP在无病生存率(P = .005)和总生存率(P = .01)方面仍优于L-PAM。接受CMFVP治疗的患者中有35%死亡,而接受L-PAM治疗的患者中有46%死亡。最大的生存获益在绝经前女性和腋窝淋巴结4个或更多阳性的女性中最为明显。CMFVP的急性毒性比L-PAM更频繁,但两种方案的毒性均可接受且可逆。长期毒性仅限于2例接受L-PAM治疗的患者和1例接受CMFVP治疗的患者出现骨髓增殖性疾病。1979年启动的第二代系列研究根据淋巴结状态、雌激素受体(ER)状态和绝经状态进行设计。我们将ER阴性、淋巴结阴性的患者随机分为接受6个月联合化疗或不接受治疗。由于入组缓慢,该研究已结束,患者现正进入与东部肿瘤协作组进行的类似组间研究。我们将ER阴性、淋巴结阳性的患者随机分为接受1年或2年的CMFVP治疗。(摘要截短于250字)

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