Drug delivery in acute myeloid leukemia.

Johannes Kohlschütter, Stefan Michelfelder, Martin Trepel
Author Information
  1. Johannes Kohlschütter: University Medical Center Hamburg-Eppendorf, Department of Oncology and Hematology, Martinistrasse 52, D-20246 Hamburg, Germany.

Abstract

BACKGROUND: Acute myeloid leukemia was among the first malignancies to be cured by drug therapy alone, but overall survival rates remain unsatisfactory and have changed little over the past 20 years. Conventional chemotherapeutic regimens, which almost invariably include cytarabine and anthracyclines, are untargeted, and more specific therapies are needed.
OBJECTIVE: We have chosen acute myeloid leukemia as a disease prototype to review established and novel targeted approaches in leukemia treatment.
METHODS: Our selection of the reviewed literature focused on drug delivery aspects.
CONCLUSION: While the toxicity profile of chemotherapeutics has been improved by liposomal formulations and antibody conjugation for leukemia-directed uptake, their efficacy has probably not changed significantly. Drugs with an alternative mode of action, including kinase inhibitors, hold great promise. Further improvements may result from the characterization of novel acute myeloid leukemia (AML) cell surface receptors and of leukemic stem cells, as well as from the design of leukemia-targeted gene therapy vectors.

MeSH Term

Antibodies, Monoclonal
Antigens, CD
Antigens, Differentiation, Myelomonocytic
Antineoplastic Agents
Drug Delivery Systems
Genetic Therapy
Humans
Integrin alpha4beta1
Leukemia, Myeloid, Acute
Liposomes
Neoplastic Stem Cells
Sialic Acid Binding Ig-like Lectin 3

Chemicals

Antibodies, Monoclonal
Antigens, CD
Antigens, Differentiation, Myelomonocytic
Antineoplastic Agents
CD33 protein, human
Integrin alpha4beta1
Liposomes
Sialic Acid Binding Ig-like Lectin 3

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