Volume 60, Issue 4 pp. 242-246
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Adjuvant six cycles of high-dose adriamycin, cyclophosphamide, methotrexate, 5-fluorouracil (ACMF) vs. 12 cycles of low-dose acmf with tamoxifen for premenopausal, node-positive breast cancer patients: Results of a prospective randomized study

Dr. Takashi Fukutomi MD

Corresponding Author

Dr. Takashi Fukutomi MD

Department of Surgery, National Cancer Center Hospital, Tokyo, Japan

Department of Surgery, National Cancer Center Hospital, 5–1–1, Tsukiji, Chuo-Ku, Tokyo 104, JapanSearch for more papers by this author
Sadako Akashi MD

Sadako Akashi MD

Department of Surgery, National Cancer Center Hospital, Tokyo, Japan

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Takeshi Nanasawa MD

Takeshi Nanasawa MD

Department of Surgery, National Cancer Center Hospital, Tokyo, Japan

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Hiroshi Yamamoto MD

Hiroshi Yamamoto MD

Department of Surgery, National Cancer Center Hospital, Tokyo, Japan

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First published: December 1995
Citations: 3

Abstract

A prospective randomized study was conducted to compare the adjuvant efficacy of six cycles of high-dose ACMF (Adriamycin, ADM; cyclophosphamide, CPA; methotrexate, MTX; 5-fluorouracil, 5-FU) with that of 12 cycles of low-dose ACMF in premenopausal, node-positive breast cancer patients. The six-cycle ACMF group (93 patients) received, intravenously (iv), 130 mg/m2 CPA, 26 mg/m2 MTX, and 600 mg/m2 5-FU on days 1 and 8, and 26 mg/m2 ADM on day 1 of each cycle. The 12-cycle ACMF group (97 patients) received, iv, 65 mg/m2 CPA, 13 mg/m2 MTX, and 300 mg/m2 5-FU on days 1 and 8, and 13 mg/m2 ADM on day 1 of each cycle. These treatments were repeated every 4 weeks, and all the patients took tamoxifen (30 mg/day) for 2 years. The background factors of the two groups were comparable. There were non-significant trends toward better disease-free and overall survival rates in the high-dose, six-cycle ACMF group. Both treatments were well tolerated, but more patients in the low-dose, 12-cycle group refused to continue to receive chemotherapy. These data suggest that escalating doses of ACMF over a shorter period, even with doses within the conventional range, are superior to low-dose, prolonged therapy. © 1995 Wiley-Liss, Inc.

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