FLT3阳性急性髓性白血病患者的转归巴基斯坦卡拉奇一家三级保健医院的经验。

Maria Zulfiqar, Natasha Ali, Usman Shaikh, Hamzah Jehanzeb, Salman Arif, Zurrya Fasih Khan, Nabiha Saeed, Zeeshan Ansar
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摘要

简介:急性髓性白血病(AML)的分子遗传异常对疾病诊断和决定预后和临床病程至关重要。FLT3和核磷蛋白(NPM)基因的突变是最常见的遗传异常,也已知会影响疾病结局。在大约30%的新发AML患者中发现FLT3突变,并与预后不良相关。本研究旨在确定flt3阳性AML患者对诱导化疗的反应、总生存期(OS)和复发率(RR)。材料与方法:本研究回顾性分析了2015年1月至2022年7月登记的75例新诊断的AML患者。记录患者人口统计学和临床血液学参数,并对FLT3、ITD/TKD和NPM突变进行分子分析。所有患者均接受标准诱导化疗,并评估其治疗反应、OS和RR。结果:共分析了75例急性髓性白血病。样本平均年龄34.9岁,其中男性65.3%,女性34.7%。将患者分为两组:FLT3阳性而NPM阴性(FLT3+/NPM-)组,占17.3%;FLT3和NPM均阴性(FLT3-/NPM-)组,占82.7%。诱导后第28天,FLT3阳性组完全缓解率为69.2%,FLT3阴性组完全缓解率为77.4%。在FLT3+/NPM-组中,55.6%在第28天缓解的病例随后复发,而FLT3-/NPM-的病例为50.0%。该队列和FLT3+组的总中位生存时间为1467天,而FLT3组的中位生存时间由于非常高的存活率而无法估计。结论:与FLT3阴性患者相比,FLT3阳性患者的预后无显著差异。
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Outcomes of Patients with FLT3 Positive Acute Myeloid Leukaemia; an Experience from a Tertiary Care Hospital in Karachi, Pakistan.

Introduction: Molecular genetic abnormalities in acute myeloid leukaemia (AML) are essential for disease diagnosis and determining prognosis and clinical course. Mutations in FLT3 and nucleophosmin (NPM) genes are the most frequent genetic abnormalities, which are also known to impact disease outcomes. FLT3 mutations have been identified in approximately 30% of de novo AML patients and are associated with poor prognoses. This study aimed to determine the response to induction chemotherapy, overall survival (OS) and relapse rate (RR) in patients with FLT3-positive AML.

Materials and methods: In this study, a retrospective analysis was performed of 75 newly diagnosed patients with AML registered between January 2015 and July 2022. Patient demographics and clinical-haematological parameters were noted and molecular analysis for FLT3 ITD/TKD and NPM mutations was performed. All the patients received standard induction chemotherapy and their response to treatment, OS and RR were assessed.

Results: A total of 75 cases of AML were analysed. The mean age of the sample was 34.9 years, of which 65.3% were males and 34.7% were females. The patients were stratified into two groups: Those who were positive for FLT3 while negative for NPM (FLT3+/NPM-), representing 17.3% and those who were negative for both FLT3 and NPM (FLT3-/NPM-), representing 82.7% of cases. On day 28 post-induction, the complete remission rate was 69.2% in the FLT3 positive group and 77.4% in the FLT3 negative group. In the FLT3+/NPM- group, 55.6% of cases who were in remission at day 28 subsequently relapsed, compared to 50.0% of FLT3-/NPM- cases. The overall median survival time for the cohort and FLT3+ group was 1467 days, while that of the FLT3-group could not be estimated due to the very high survival rate.

Conclusion: No significant differences in outcomes were observed in patients who were FLT3 positive compared to those who were FLT3 negative.

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