Nomura Y, Tashiro H, Hisamatsu K, Shinozuka K
Department of Breast Surgery, National Kyushu Cancer Center Hospital, Fukuoka, Japan.
Cancer. 1988 Jun 1;61(11):2168-75. doi: 10.1002/1097-0142(19880601)61:11<2168::aid-cncr2820611106>3.0.co;2-f.
Based on estrogen receptor (ER) status and menopausal status, operable breast cancer (International Union Against Cancer [UICC] Stage I, II, and III) patients were randomized for adjuvant endocrine therapy, chemotherapy, and chemoendocrine therapy, and the effects on the disease-free survival (DFS) and overall survival (OS) were compared. Adjuvant endocrine therapy was composed of tamoxifen (TAM) 20 mg/day orally for 2 years in postmenopausal patients. In premenopausal patients, oophorectomy (OVEX) was done before TAM administration. In the chemotherapy arm, the patients were given 0.06 mg/kg of body weight of mitomycin C (MMC) intravenously (IV) and then an oral administration of cyclophosphamide (CPA) 100 mg/body orally in an administration of a 3-month period and a 3-month intermission. This 6-month schedule was repeated four times in 2 years. As the chemoendocrine therapy arm, TAM with MMC + CPA chemotherapy was added. The patients were randomized according to ER and menopausal status. Estrogen receptor-positive (ER+) cancer patients were randomized to three arms: TAM +/- OVEX, MMC + CPA, or MMC + CPA + TAM. For estrogen receptor-negative (ER-) patients, there were two arms: MMC + CPA, or MMC + TAM. The study started in September 1978, and 692 patients entered until the end of 1984 were evaluated. The median follow-up was about 46 months. Totally, a 9.8% rate (68/692) of recurrence was noted, a 7.5% rate (52/692) of mortality. There were no significant differences in DFS or OS among the treatment arms in ER+ or ER- patients. There was significant differences in adverse effects such as bone marrow suppression, gastrointestinal disturbances, cystitis, hair loss between endocrine therapy and chemotherapy or chemoendocrine therapy groups. In this preliminary study, it was concluded that because of less adverse effects of endocrine therapy, it seems rational to select the operable breast cancer patients by the presence or absence of ER, namely, endocrine therapy for ER+ and chemotherapy for ER- cancer patients.
根据雌激素受体(ER)状态和绝经状态,将可手术乳腺癌(国际抗癌联盟[UICC] I、II和III期)患者随机分为辅助内分泌治疗、化疗和化疗内分泌治疗组,并比较其对无病生存期(DFS)和总生存期(OS)的影响。辅助内分泌治疗方案为绝经后患者口服他莫昔芬(TAM)20 mg/天,共2年。绝经前患者在服用TAM前进行卵巢切除术(OVEX)。化疗组患者静脉注射0.06 mg/kg体重的丝裂霉素C(MMC),然后口服环磷酰胺(CPA)100 mg/天,给药3个月,间歇3个月。这种6个月的疗程在2年内重复4次。化疗内分泌治疗组在TAM基础上加用MMC + CPA化疗。患者根据ER和绝经状态进行随机分组。雌激素受体阳性(ER+)癌症患者随机分为三组:TAM +/- OVEX、MMC + CPA或MMC + CPA + TAM。雌激素受体阴性(ER-)患者分为两组:MMC + CPA或MMC + TAM。该研究于1978年9月开始,对截至1984年底入组的692例患者进行了评估。中位随访时间约为46个月。总体而言,复发率为9.8%(68/692),死亡率为7.5%(52/692)。ER+或ER-患者的各治疗组之间在DFS或OS方面无显著差异。内分泌治疗组与化疗组或化疗内分泌治疗组在骨髓抑制、胃肠道紊乱、膀胱炎、脱发等不良反应方面存在显著差异。在这项初步研究中,得出的结论是,由于内分泌治疗的不良反应较少,根据ER的有无来选择可手术乳腺癌患者似乎是合理的,即ER+癌症患者采用内分泌治疗,ER-癌症患者采用化疗。