Bleomycin, vinorelbine and trofosfamide in relapsed stage IV cutaneous malignant melanoma patients |
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Authors: | Jens Atzpodien Lars Morawek Michael Fluck Martina Reitz |
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Affiliation: | 1. Fachklinik Hornheide an der Westf?lischen Wilhelms-Universit?t Münster, Dorbaumstr. 300, 48157, Münster, Germany 2. Europ?isches Institut für Tumor Immunologie und Pr?vention (EUTIP), Mühlenpfad 5, Bad Honnef, Germany
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Abstract: | Purpose To evaluate the efficacy of bleomycin, vinorelbine, and trofosfamide (BVT) in 28 patients with pretreated relapsed AJCC stage IV cutaneous malignant melanoma. Methods Patients in relapse after first- or second-line therapy received 8 mg/m2 intravenous (i.v.) bleomycin, 25 mg/m2 i.v. vinorelbine, on days 1 and 6, each, and oral (p.o.) trofosfamide 60 mg/m2/day, days 1–7. BVT therapy was repeated every 5 weeks until progression of disease occurred. A maximum of six BVT cycles (mean, 2.2 cycles) was administered per patient. Results Three patients (11%) reached a partial response; 5 (18%) patients showed stable disease, and 20 (71%) patients progressed upon BVT therapy. Median overall survival of all 28 patients was 6 months (6-month survival rate, 52%). Patients with partial remission or stable disease (n = 8) exhibited a median overall survival of 10 months (6-month survival rate, 75%), while patients with disease progression (n = 20) showed a median overall survival of 3 months (6-month survival rate, 43%). Most side effects were limited to WHO grade I/II mild anemia, leucocytopenia, fatigue, nausea/vomiting, pain, and anorexia. WHO grade III/IV side effects occurred in 7% (anorexia) and 4% (fatigue) of patients. Conclusion Treatment with BVT was efficient in 29% of pretreated relapsed stage IV cutaneous melanoma patients, with overall good tolerability and safety. |
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Keywords: | Melanoma Bleomycin, vinorelbine, and trofosfamide |
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