Skip to main navigation Skip to search Skip to main content

Experience with gemtuzumab ozogamycin ("mylotarg") and all-trans retinoic acid in untreated acute promyelocytic leukemia

  • Elihu H. Estey
  • , Francis J. Giles
  • , Miloslav Beran
  • , Susan O'Brien
  • , Sherry A. Pierce
  • , Stefan H. Faderl
  • , Jorge E. Cortes
  • , Hagop M. Kantarjian
  • The University of Texas Health Science Center at Houston
  • Department of Cancer Biology

Research output: Contribution to a Journal (Peer & Non Peer)Articlepeer-review

178 Citations (Scopus)

Abstract

We administered gemtuzumab ozogamycin ("mylotarg"; 9 mg/m2 day 1 or 5) and all-trans retinoic acid (ATRA) to 19 patients with untreated acute promyelocytic leukemia (APL). There were 3 patients who also received idarubicin because of a white blood cell (WBC) count of more than 30 000/μL. In complete remission (CR), patients were to receive 8 courses of mylotarg (9 mg/m2 every 4 to 5 weeks) and ATRA; idarubicin was added only for persistent or recurrent polymerase chain reaction (PCR) positivity. The CR rate was 16/19 (84%). All 12 patients tested to date were PCR-negative 2 to 4 months from CR date; none of the 7 patients evaluated subsequently have reverted to PCR positivity (median follow-up in CR was 5 months, up to 14 months). Mylotarg was well tolerated. A median of 5 post-CR courses have been given to date with 3 patients having currently received 8 post-CR courses, and 4 patients receiving 7 post-CR courses. Mylotarg appears active in APL, and repeated administration is feasible.

Original languageEnglish
Pages (from-to)4222-4224
Number of pages3
JournalBlood
Volume99
Issue number11
DOIs
Publication statusPublished - 1 Jun 2002
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Fingerprint

Dive into the research topics of 'Experience with gemtuzumab ozogamycin ("mylotarg") and all-trans retinoic acid in untreated acute promyelocytic leukemia'. Together they form a unique fingerprint.

Cite this