
We report on an 66-year old female in whom we diagnosed uterine carcinosarcoma and concurrent breast cancer. As first-line treatment the patient received ifosfamide 4.8 mg/m2 body surface. During her second course of chemotherapy she developed sequentially life-threatening toxicities; severe emesis followed by nephrotoxicity, neurotoxicity and myelosuppression. Early prophylactic administration of rhG-CSF (Filgrastim) helped to overcome severe, potentially fatal myelosuppression. The course of severe toxicities following high doses of ifosfamide might reflect a dependent sequence, where one organ failure causes a subsequent organ failure. Prophylactic treatment of anticipated toxicity should be considered for the management of severe ifosfamide-induced toxicity. Such treatment may consist of sufficient antiemesis, sufficient hydration, as well as a therapy with methylene blue in case of severe neurotoxicity.
Dose-Response Relationship, Drug, Filgrastim, Multiple Organ Failure, Carcinoma, Ductal, Breast, Breast Neoplasms, Combined Modality Therapy, Drug Administration Schedule, Recombinant Proteins, Neoplasms, Multiple Primary, Granulocyte Colony-Stimulating Factor, Uterine Neoplasms, Humans, Female, Ifosfamide, Antineoplastic Agents, Alkylating, Aged, Neoplasm Staging
Dose-Response Relationship, Drug, Filgrastim, Multiple Organ Failure, Carcinoma, Ductal, Breast, Breast Neoplasms, Combined Modality Therapy, Drug Administration Schedule, Recombinant Proteins, Neoplasms, Multiple Primary, Granulocyte Colony-Stimulating Factor, Uterine Neoplasms, Humans, Female, Ifosfamide, Antineoplastic Agents, Alkylating, Aged, Neoplasm Staging
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