All-trans-Retinoic Acid in Acute Promyelocytic Leukemia

Acute promyelocytic leukemia is a distinct subtype of acute myeloid leukemia 1 in which a balanced reciprocal translocation between chromosomes 15 and 17 results in the union of portions of the promyelocytic leukemia gene with the gene for retinoic acid receptor alpha. 2 This chimeric gene encodes t...

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Veröffentlicht in:The New England journal of medicine 1997-10, Vol.337 (15), p.1021-1028
Hauptverfasser: Tallman, Martin S, Andersen, Janet W, Schiffer, Charles A, Appelbaum, Frederick R, Feusner, James H, Ogden, Angela, Shepherd, Lois, Willman, Cheryl, Bloomfield, Clara D, Rowe, Jacob M, Wiernik, Peter H
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Sprache:eng
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Zusammenfassung:Acute promyelocytic leukemia is a distinct subtype of acute myeloid leukemia 1 in which a balanced reciprocal translocation between chromosomes 15 and 17 results in the union of portions of the promyelocytic leukemia gene with the gene for retinoic acid receptor alpha. 2 This chimeric gene encodes the promyelocytic leukemia–retinoic acid receptor alpha fusion protein. 3 – 6 Although 65 to 80 percent of patients with acute promyelocytic leukemia have a complete remission with standard chemotherapy, 7 , 8 approximately 10 to 20 percent die either before or during chemotherapy of bleeding attributable to disseminated intravascular coagulation, fibrinolysis, and proteolysis. 9 All- trans -retinoic acid differentiates leukemic . . .
ISSN:0028-4793
1533-4406
DOI:10.1056/NEJM199710093371501