Abstract
To evaluate a regimen including high-dose mitoxantrone in previously untreated adults with AML, 45 patients aged 21-59 (median 41) were given cytarabine, 3 g/m2 days 1-5, mitoxantrone, 80 mg/m2 day 2 and etoposide, 150 mg/m2 days 1,3,5. Post-remission therapy consisted of 5 cycles combining the same agents at reduced doses. Complete remission was seen in 36 patients. The observed 3-year survival is 28%. Cytogenetic pattern and CD34 expression correlated with response and survival. Significant toxicity included myelosuppression, mucositis, diarrhea and hyperbilirubinemia. Ventricular ejection fraction was generally reduced, with clinical cardiac dysfunction in only 2 patients. This high-dose mitoxantrone combination can be administered to young adults with AML with tolerable toxicity and results comparable to those of other dose-intensive regimens.
Publication types
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Clinical Trial
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Clinical Trial, Phase II
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Actuarial Analysis
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Acute Disease
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Adult
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Antineoplastic Combined Chemotherapy Protocols / adverse effects
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Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
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Bone Marrow Transplantation
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Combined Modality Therapy
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Conjunctivitis / chemically induced
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Cytarabine / administration & dosage
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Cytarabine / adverse effects
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Disease-Free Survival
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Etoposide / administration & dosage
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Etoposide / adverse effects
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Female
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Gastrointestinal Diseases / chemically induced
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Humans
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Hyperbilirubinemia / chemically induced
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Leukemia, Myeloid / drug therapy*
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Leukemia, Myeloid / mortality
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Leukemia, Myeloid / therapy
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Male
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Methylprednisolone / administration & dosage
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Middle Aged
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Mitoxantrone / administration & dosage*
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Mitoxantrone / adverse effects
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Remission Induction
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Risk
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Stomatitis / chemically induced
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Stroke Volume / drug effects
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Survival Analysis
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Survival Rate
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Treatment Outcome
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Tretinoin / administration & dosage
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Ventricular Dysfunction, Left / chemically induced
Substances
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Cytarabine
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Tretinoin
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Etoposide
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Mitoxantrone
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Methylprednisolone