A combination of drugs may prove
to be a more effective treatment for chronic myelogenous leukemia
New research discovers a combination of drugs that may
prove to be a more effective treatment for a lethal form of leukemia. The study,
published by Cell Press in the May issue of the journal Cancer Cell, reports that
the new therapeutic strategy effectively targets notoriously intractable leukemia
stem cells that often escape standard treatment and are a main factor in disease
relapse.
Chronic myelogenous leukemia (CML) is a deadly form of
leukemia that is associated with chromosome rearrangements that result in the
expression of the BCR-ABL oncoprotein. "Treatment of CML with the BCL-ABL
inhibitor imatinib mesylate (IM, Gleevec) has emerged as the first-line treatment
for patients with CML," explains senior study author Dr. Ravi Bhatia, the
director of Stem Cell and Leukemia Research at the City of Hope National Medical
Center in Duarte, California. "However, although most CML patients initially
respond well to IM treatment, there is evidence that primitive quiescent leukemia
stem cells are retained in patients achieving remission after IM treatment and
that these stem cells are responsible for disease recurrence."
Dr. Bhatia and colleagues were interested in examining
whether histone deacetylase inhibitors (HDACi) that have shown some promise as
a treatment for several other cancers, might be effective at eliminating CML stem
cells. HDACi were of interest because they not only target rapidly dividing cancer
cells but also have been shown to eliminate non-proliferating cancer cells. The
researchers found that treatment with a combination of HDACi and IM effectively
reduced CML cells that were resistant to IM alone. Further, a combination of HDACi
and IM markedly diminished leukemia stem cells in a mouse model of CML.
The group went on to show that the interaction of HDACi
and IM inhibited genes involved in regulating leukemia stem cell survival. "Our
studies indicate that treatment with HDACi combined with IM is effective against
CML leukemia stem cells that resist elimination by IM alone," concludes Dr.
Bhatia. "Several HDACi are in clinical development, and our studies support
clinical trials of HDACi in combination with tyrosine kinase inhibitors to eliminate
leukemia stem cells in patients with CML."
The researchers include Bin Zhang, City of Hope National
Medical Center, Duarte, CA; Adam C. Strauss, City of Hope National Medical Center,
Duarte, CA; Su Chu, City of Hope National Medical Center, Duarte, CA; Min Li,
City of Hope National Medical Center, Duarte, CA; Yinwei Ho, City of Hope National
Medical Center, Duarte, CA; Keh-Dong Shiang, City of Hope National Medical Center,
Duarte, CA; David S. Snyder, City of Hope National Medical Center, Duarte, CA;
Claudia S. Huettner, Dana-Farber Cancer Institute, Boston, MA; Leonard Shultz,
The Jackson Laboratory, Bar Harbor, ME; Tessa Holyoake, University of Glasgow,
Scotland, UK; and Ravi Bhatia, City of Hope National Medical Center, Duarte, CA.
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