MITOXANTRONE, VINCRISTINE, AND 5-FLUOROURACIL WITH LEUCOVORIN MODULATION AS INDUCTION CHEMOTHERAPY PRIOR TO HIGH-DOSE INTENSIFICATION IN METASTATIC BREAST-CANCER

Citation
Sf. Williams et al., MITOXANTRONE, VINCRISTINE, AND 5-FLUOROURACIL WITH LEUCOVORIN MODULATION AS INDUCTION CHEMOTHERAPY PRIOR TO HIGH-DOSE INTENSIFICATION IN METASTATIC BREAST-CANCER, Breast cancer research and treatment, 28(3), 1993, pp. 291-294
Citations number
6
Categorie Soggetti
Oncology
ISSN journal
01676806
Volume
28
Issue
3
Year of publication
1993
Pages
291 - 294
Database
ISI
SICI code
0167-6806(1993)28:3<291:MVA5WL>2.0.ZU;2-8
Abstract
We treated 39 women with newly diagnosed stage IV breast cancer with a new regimen of mitoxantrone 18 mg/m(2) on days 1, 29, 57, vincristine 1.4 mg/m(2) (maximum 2.0 mg) on days 1, 8, 15, 22, 29, 36, 43, 50, an d 5-fluorouracil 375 mg/m(2) on days 15-20, 43-47, 71-75 with leucovor in modulation 500 mg/m(2) before each 5FU infusion (MVF). This regimen was utilized as an initial cytoreductive or induction program for the se patients prior to high-dose intensification with autologous stem ce ll rescue. Ten patients (25%) obtained a clinical complete response an d six patients (15%) obtained a partial response for an overall respon se rate of 40%. In addition, 10 patients had evaluable disease that wa s improved or stable (primarily bone and/or bone marrow metastases) af ter MVF induction. Thus, 26 patients (65%) were eligible for high-dose intensification with autologous stem cell rescue after MVF induction. Toxicity was primarily a mild mucositis and more commonly peripheral neuropathy. MVF therapy is an active treatment program for metastatic breast cancer but the neurotoxicity makes it difficult to recommend fo r widespread use.