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Arsenic derivatives in hematologic malignancies: a role beyond acute promyelocytic leukemia?
Author(s) -
Verstovsek Srdan,
Giles Francis,
QuintásCardama Alfonso,
Perez Nichole,
RavandiKashani Farhad,
Beran Miloslav,
Freireich Emil,
Kantarjian Hagop
Publication year - 2006
Publication title -
hematological oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.918
H-Index - 44
eISSN - 1099-1069
pISSN - 0278-0232
DOI - 10.1002/hon.787
Subject(s) - arsenic trioxide , acute promyelocytic leukemia , medicine , hematologic neoplasms , myelodysplastic syndromes , multiple myeloma , hematologic disease , leukemia , disease , hematologic malignancy , arsenic , oncology , cancer research , cancer , chemistry , bone marrow , gene , retinoic acid , biochemistry , organic chemistry
The importance of arsenic trioxide (As 2 O 3 ) has been underscored over the last decade due to its efficacy against acute promyelocytic leukemia (APL), a disease in which this agent has been associated with complete hematologic and molecular remission rates of 87% and 83%, respectively. The different molecular mechanisms of action of As 2 O 3 suggest its applicability in hematologic malignancies other than APL. However, responses obtained thus far have consisted of improvements in signs and symptoms without the elimination of a given disease. Toxicities derived from As 2 O 3 are significant but manageable and reversible. However, the risk/benefit ratio of As 2 O 3 in hematologic malignancies other than APL is still unclear. The development of new generations of orally bioavailable inorganic, as well as new organic, arsenic compounds with improved toxicity profiles may bolster the therapeutic application of arsenic derivatives in hematologic malignancies such as leukemia, multiple myeloma and myelodysplastic syndromes. Copyright © 2006 John Wiley & Sons, Ltd.

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