Sudden death among patients with acute promyelocytic leukemia treated with arsenic trioxide

Author:

Westervelt Peter1,Brown Randy A.1,Adkins Douglas R.1,Khoury Hanna1,Curtin Peter1,Hurd David1,Luger Selina M.1,Ma Margaret K.1,Ley Timothy J.1,DiPersio John F.1

Affiliation:

1. From the Division of Bone Marrow Transplantation and Stem Cell Biology, and the Division of Molecular Oncology, Washington University School of Medicine, St Louis, MO; Division of Hematology/Oncology, Oregon Health Sciences University, Portland; Division of Hematology/Oncology, Comprehensive Cancer Center of Wake Forest University, Winston-Salem, NC; and Division of Hematology/Oncology, University of Pennsylvania School of Medicine, Philadelphia.

Abstract

Arsenic trioxide has been shown to be effective in treating acute promyelocytic leukemia (APL), with minimal overall toxicity reported to date. A phase I/II study was initiated in June 1998 using arsenic trioxide for relapsed APL to determine the maximum tolerated or minimal effective dose and to determine the efficacy of treatment at that dose. Ten patients received 1 to 4 monthly cycles of treatment with 0.1 mg/kg per day intravenous arsenic trioxide. Six of 7 patients evaluable for response achieved cytogenetic or molecular complete remission. However, 3 patients died suddenly during the first cycle of treatment. Autopsies obtained on 2 of these failed to identify a cause of sudden death, despite evidence of pulmonary hemorrhage in one. A third patient, for whom an autopsy was not performed, became asystolic and died while on continuous cardiac telemetry. These observations suggest that arsenic trioxide may be significantly or even fatally toxic at doses currently used and that caution is warranted in its use.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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