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Antibody-targeted chemotherapy of older patients with acute myeloid leukemia in first relapse using Mylotarg (gemtuzumab ozogamicin)

  • Mylotarg Study Group
  • The University of Chicago
  • KU Leuven
  • University of Texas MD Anderson Cancer Center
  • Wayne State University
  • University of Pennsylvania
  • Fred Hutchinson Cancer Research Center
  • University of Washington
  • Hospital Saint Joseph
  • University of Rochester
  • Pfizer
  • HematoLogics Inc
  • Erasmus University Rotterdam
  • Université Paris Cité
  • Centre Hospitalier Régional
  • Northwestern University
  • Johannes Gutenberg University Mainz
  • Hospital A Mignot
  • Technische Universität Dresden
  • Friedrich-Alexander University Erlangen-Nürnberg
  • Hospital Durán i Reynals
  • Academic Medical Center
  • Linköping University
  • Hôpital Maisonneuve-Rosemont
  • City of Hope National Med Center
  • Karolinska Institutet
  • University of Cologne
  • Ospedale Mauriziano Umberto I
  • University of Wales
  • Université de Lille
  • University of Miami
  • Stony Brook University
  • Stanford University
  • University of Michigan, Ann Arbor
  • Hospital Clínic de Barcelona
  • University of Genoa
  • University College Hospital
  • Medizinische Hoschule Hannover
  • Städt Krankenhaus
  • University of Arizona
  • Hospital Clínico San Carlos de Madrid
  • Princess Margaret Cancer Centre
  • University Institute of Architecture of Reggio Calabria
  • Institutio Portugues de Oncologia
  • Huddinge sjh
  • Northwell Health System

Research output: Contribution to journalArticlepeer-review

215 Scopus citations

Abstract

We analyzed the safety and efficacy of Mylotarg (gemtuzumab ozogamicin, an antibody-targeted chemotherapy consisting of a humanized anti-CD33 antibody linked to calicheamicin, a potent antitumor antibiotic) in the treatment of 101 patients ≥60 years of age with acute myeloid leukemia (AML) in untreated first relapse in three open-label trials. Mylotarg is administered as a 2-h intravenous infusion at 9 mg/m2 for two doses with 14 days between doses. The overall remission rate was 28%, with complete remission (CR) in 13% of patients and complete remission with incomplete platelet recovery (CRp) in 15%. Median survival was 5.4 months for all patients and 14.5 months and 11.8 months for patients achieving CR and CRp, respectively. CD33 antigen is present on normal hematopoietic progenitor cells; thus, an expected high incidence of grade 3 or 4 neutropenia (99%) and thrombocytopenia (99%) was observed. The incidences of grade 3 or 4 elevations of bilirubin and hepatic transaminases were 24% and 15%, respectively. There was a low incidence of grade 3 or 4 mucositis (4%) and infections (27%) and no treatment-related cardiotoxicity, cerebellar toxicity, or alopecia. Mylotarg is an effective treatment for older patients with CD33-positive AML in first relapse and has acceptable toxicity.

Original languageEnglish
Pages (from-to)1627-1636
Number of pages10
JournalLeukemia
Volume16
Issue number9
DOIs
StatePublished - 2002

Keywords

  • Antibody-targeted chemotherapy
  • CD33-positive acute myeloid leukemia
  • Calicheamicin
  • Gemtuzumab ozogamicin
  • Humanized anti-CD33 antibody
  • Therapeutic trials

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