Mathews Vikram, Thomas Maria, Srivastava Vivi M, George Biju, Srivastava Alok, Chandy Mammen
Department of Haematology, Christian Medical College, Vellore, 632004 India.
Haematologica. 2007 Jul;92(7):994-5. doi: 10.3324/haematol.10802.
Ninety-eight newly diagnosed cases of PML-RARalpha positive APL were treated with a regimen of single agent ATO. FLT3 activating mutations were seen in 33% and an additional cytogenetic finding was noted in 23.2%. FLT3 activating mutations were significantly associated with a bcr3 PML-RARalpha isoform (p=0.012) and a delay in achieving a molecular remission (p=0.022). Neither FLT3 activating mutations nor secondary cytogenetic changes had an impact on clinical outcome.
98例新诊断的PML-RARα阳性急性早幼粒细胞白血病患者接受了单药三氧化二砷治疗方案。33%的患者出现FLT3激活突变,23.2%的患者有其他细胞遗传学发现。FLT3激活突变与bcr3 PML-RARα异构体显著相关(p=0.012),且在实现分子缓解方面出现延迟(p=0.022)。FLT3激活突变和继发性细胞遗传学改变均未对临床结局产生影响。