Best Practice & Research Clinical Haematology
Volume 21, Issue 1 , Pages 29-41, March 2008

New approaches in acute myeloid leukemia

  • William Blum, MD (Assistant Professor of Medicine)

      Affiliations

    • Corresponding Author InformationCorresponding author. Tel.: +1 614 293 9273; Fax: +1 614 293 7526.
  • ,
  • Guido Marcucci, MD (Associate Professor of Medicine)

Division of Hematology and Oncology, Department of Internal Medicine, Comprehensive Cancer Center, The Ohio State University, Columbus, OH 43210, USA

Today, treatment of patients with acute myeloid leukemia (AML) remains predominantly a “one-fits-all” approach with intensive cytarabine-based chemotherapy as the mainstay, but we are finally beginning to reap the rewards of decades of basic, translational, and clinical research. Developing individualized, “targeted” therapy for each AML patient based on unique molecular features of disease remains a daunting goal, yet one that we can now begin to envision. Hypothesis-based study designs—from preclinical/laboratory experiments to phase 1 and subsequent efficacy trials—provide the foundation for advances in the diagnosis, risk stratification, and treatment of patients with AML. The following is an outline of several key areas of ongoing AML research.

Key words: acute myeloid leukemia, epigenetics, targeted therapy, ribonucleotide reductase, G3139 (oblimersen sodium, Genasense), core binding factor, KIT mutation, RAS mutation

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S1521-6926(07)00099-0

doi:10.1016/j.beha.2007.11.009

Best Practice & Research Clinical Haematology
Volume 21, Issue 1 , Pages 29-41, March 2008