| Literature DB >> 26183877 |
Yinjun Lou1, Yafang Ma1, Shanshan Suo1, Wanmao Ni1, Yungui Wang1, Hanzhang Pan1, Hongyan Tong1, Wenbin Qian1, Haitao Meng1, Wenyuan Mai1, Jian Huang1, Wenjuan Yu1, Juyin Wei1, Liping Mao1, Jie Jin2.
Abstract
Prognostic factors for patients with acute promyelocytic leukemia (APL) treated in the context of arsenic trioxide (ATO)-based frontline regimes have not been established clearly. We retrospectively analyzed the clinical features, immunophenotypes, Fms-like tyrosine kinase-3 internal tandem duplication (FLT3-ITD), and outcomes of 184 consecutive newly diagnosed APL patients treated by intravenous ATO-based therapy. The median age was 40 years (14-77 years). The early death rate was 4.9% (9/184 patients). With a median follow-up time of 36 months (9-74 months), the 3-year relapse-free survival (RFS) and overall survival (OS) were 93.3% and 92.2%, respectively. Interestingly, there was no meaningful association between 3-year RFS and initial white blood cell count, FLT3-ITD status, or type of PML-RARA isoforms. In multivariable analysis, the CD56 expression was the only independent risk factor in terms of RFS (hazard ratio, 4.70; P=0.005). These results suggested that ATO-based therapy may ameliorate the unfavorable influence of previously known high-risk features; moreover, CD56 expression remains to be a potentially unfavorable prognostic factor in APL patients.Entities:
Keywords: Acute promyelocytic leukemia; Arsenic trioxide; CD56 expression; FLT3 mutation; Prognostic factors
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Year: 2015 PMID: 26183877 DOI: 10.1016/j.leukres.2015.05.016
Source DB: PubMed Journal: Leuk Res ISSN: 0145-2126 Impact factor: 3.156