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Induction therapy of AML with ara-C plus daunorubicin versus ara-C plus gemtuzumab ozogamicin: a randomized phase II trial in elderly patients
Affiliation:1. Department of Medicine, Hematology and Oncology, University Hospital Frankfurt, Frankfurt;2. Department of Medicine A, Hematology and Oncology, University Hospital Muenster, Muenster;3. Department of Medicine, Hematology and Oncology, University Hospital Essen, Essen;4. St. Marien-Hospital, Hamm;5. Institute for Biostatistics and Clinical Research, University of Muenster, Muenster;6. Pfizer Pharma GmbH, Berlin;7. Department of Medicine, Hematology and Oncology, University Hospital Dresden, Dresden, Germany
Abstract:BackgroundChemotherapy for elderly patients with acute myeloid leukemia (AML) results in a median overall survival (OS) of ≤1 year. Elderly patients often present with cardiac comorbidity. Gemtuzumab ozogamicin (GO) is active in elderly (≥60 years) patients with relapsed AML with low cardiac toxicity.Patients and methodsThis randomized phase II study compared a standard combination of ara-C and daunorubicin (DNR; 7+3) versus ara-C plus gemtuzumab ozogamicin (7+GO) as the first course of induction therapy. Primary objectives were comparison of blast clearance on day 16, event-free survival (EFS), and remission duration. OS, complete remission (CR), and tolerability were secondary objectives.ResultsOne hundred and nineteen patients with de novo AML, treatment-related AML, AML with a history of myelodysplastic syndrome (MDS), or high-risk MDS entered the study. Median age of 115 patients (intent-to-treat population) was 69 years. Protocol outlined a second course 7+3 for patients without blast clearance and two courses of high-dose ara-C consolidation upon CR. Both treatments were equally effective in blast clearance, CR, EFS, remission duration, or OS (median: 7+3, 9 months; 7+GO, 10 months). Induction death rate was higher in the GO group due to veno-occlusive disease.ConclusionThe study did not show significant superiority of 7+GO over standard 7+3.
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