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Gewählte Publikation:

Scheithauer, W; Dittrich, C; Kornek, G; Haider, K; Linkesch, W; Gisslinger, H; Depisch, D.
Phase II study of amonafide in advanced breast cancer.
Breast Cancer Res Treat. 1991; 20(1):63-67 Doi: 10.1007/BF01833358
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Co-Autor*innen der Med Uni Graz
Linkesch Werner
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Abstract:
Twenty-eight patients with advanced breast cancer refractory to prior hormone and/or first-line chemotherapy (with or without anthracycline drugs) were treated with the investigational agent amonafide at a dose of 800 mg/m2 intravenously over 3 hours repeated every 4 weeks. Five objective tumour responses of 5.0 months' median duration were observed in the 20 patients without previous anthracycline exposure, including 1 CR. Leukopenia was the dose-limiting toxicity; though it was generally modest with the 800 mg/m2 amonafide starting dose, an initial dose reduction should be considered in patients with prior radiotherapy and/or bone marrow involvement. Other adverse reactions included nausea/vomiting (53%), phlebitis/erythema along the vein injected (7%), and mild neurotoxic symptoms during the drug administration such as headache, tinnitus, and diaphoresis (21%). Amonafide is an active compound for the treatment of patients with advanced breast cancer and should be considered for further evaluation and incorporation in combination chemotherapy.
Find related publications in this database (using NLM MeSH Indexing)
Adult -
Aged -
Antineoplastic Agents - administration and dosage
Breast Neoplasms - drug therapy
Cardiomyopathies - chemically induced
Drug Evaluation - chemically induced
Female - chemically induced
Humans - chemically induced
Imides - chemically induced
Infusions, Intravenous - chemically induced
Isoquinolines - administration and dosage
Leukopenia - chemically induced
Middle Aged - chemically induced
Naphthalimides - chemically induced
Nausea - chemically induced

Find related publications in this database (Keywords)
AMONAFIDE
ADVANCED BREAST CANCER
CHEMOTHERAPY
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