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Decitabine and venetoclax for IDH1/2‐mutated acute myeloid leukemia

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Kaushansky K, Lichtman MA, Prchal JT, Levi M, Burns LJ, Linch DC, eds. Williams Hematology. 10th ed. New York: McGraw Hill; 2020:721-748. 5. Ho PJ, Wickramasinghe SN, Rees DC, Lee… Click to show full abstract

Kaushansky K, Lichtman MA, Prchal JT, Levi M, Burns LJ, Linch DC, eds. Williams Hematology. 10th ed. New York: McGraw Hill; 2020:721-748. 5. Ho PJ, Wickramasinghe SN, Rees DC, Lee MJ, Eden A, Thein SL. Erythroblastic inclusions in dominantly inherited beta thalassemias. Blood. 1997;89(1):322-328. 6. Alloisio N, Wilmotte R, Morle L, et al. Spectrin Jendouba: an alpha II/31 spectrin variant that is associatedwith elliptocytosis and carries amutation distant from the dimer self-association site.Blood. 1992;80(3):809-815. 7. Marechal J, Wilmotte R, Kanzaki A, et al. Ethnic distribution of allele alpha LELY, a low-expression allele of red-cell spectrin alpha-gene. Br J Haematol. 1995;90(3):553-556. 8. Rifkind RA, Danon D. Heinz body anemia–an Ultrastructural study. I Heinz Body Formation. Blood. 1965;25:885-896. 9. Platt OS, Falcone JF. Membrane protein lesions in erythrocytes with Heinz bodies. J Clin Invest. 1988;82(3):1051-1058. 10. Chen M, Ye Y, Liao L, Deng X, Qiu Y, Lin F. Hereditary spherocytosis overlooked for 7 years in a pediatric patient with β-thalassemia trait and novel compound heterozygous mutations of SPTA1 gene. Hematology. 2020;25(1):438-445. 11. Adhiyanto C, Yamashiro Y, Hattori Y, et al. A new β0-thalassemia mutation (codon 102, aac>atcac) in coexistence with a heterozygous p4.2 nippon gene. Hemoglobin. 2013;37(3):227-240.

Keywords: hematology; venetoclax idh1; idh1 mutated; acute myeloid; mutated acute; decitabine venetoclax

Journal Title: American Journal of Hematology
Year Published: 2021

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