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Journal of Cancer Research and Clinical Oncology logoLink to Journal of Cancer Research and Clinical Oncology
. 1995 Mar;121(Suppl 3):R21–R24. doi: 10.1007/BF02351067

Dexverapamil as resistance modifier in acute myeloid leukaemia

R Pirker 1,, S Zöchbauer 1, H Kupper 2, A Laßmann 2, A Gsur 1, M Frass 1, G Krajnik 1, P Knöbl 1, K Lechner 1
PMCID: PMC12200899  PMID: 8698738

Abstract

In order to evaluate dexverapamil as a resistance modifier in acute myeloid leukaemia, we have added dexverapamil (4×300 mg/d orally) to DA chemotherapy (daunorubicin, cytosine arabinoside) in six patients with acute myeloid leukaemia. Two patients (1 first and 1 second relapse) achieved complete remission and two patients (1 refractory disease, 1 third relapse) showed some improvement. One patient in first relapse died due to disease progression and one drug-refractory patient remained refractory. The peak plasma levels of dexverapamil and nordexverapamil ranged from about 600 to 4100 ng/ml and from 450 to 1130 ng/ml, respectively. Major sideeffects were hypotension and sinus bradycardia. These results show the need for further evaluation of dexverapamil as a resistance modifier in acute myeloid leukaemia.

Key words: Acute myeloid leukaemia, Drug resistance, MDR1 gene, Dexverapamil, Daunorubicin

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