Introduction: The prognosis of acute myeloid leukemia (AML) is improved in the last two decades, even though induction and consolidation chemotherapy has not involved new drugs. The more effective use of well-known agents as well as refinement of supportive care during the inevitable phase of severe pancytopenia following intensive chemotherapy accounts for the reduction of treatment-related death rate. In addition, mortality due to allogeneic and autologous stem cell transplantation has also been reduced, due to adoption of more effective therapies for graft versus host disease and other transplant-related complications. Areas covered: The multitude of chromosomal and molecular abnormalities makes the treatment of AML a challenging prospect. In addition, genetic aberrations are not mutually exclusive and coexist in the leukemic cells. As a consequence, the clinical development of new biologic agents proceeds slowly. Data for this review were identified from PubMed and references from relevant articles published in English from 2000 to 2011. Expert opinion: In Phase II studies, different new agents have been found to be active in AML and are currently under investigation in Phase III trials also in combination with conventional chemotherapy. In the near future, we would have more information about the possibility of introducing new drugs into daily practice.
机构:
Mem Sloan Kettering Canc Ctr, Leukemia Serv, 1275 York Ave, New York, NY 10065 USAMem Sloan Kettering Canc Ctr, Leukemia Serv, 1275 York Ave, New York, NY 10065 USA
机构:
Hackensack Univ Med Ctr, Div Pediat Hematol Oncol, Hackensack, NJ 07601 USAHackensack Univ Med Ctr, Div Pediat Hematol Oncol, Hackensack, NJ 07601 USA
Chen, Jing
Glasser, Chana L.
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机构:
NYU Winthrop Hosp, Div Pediat Hematol Oncol, Mineola, NY 11501 USAHackensack Univ Med Ctr, Div Pediat Hematol Oncol, Hackensack, NJ 07601 USA