The role of CBFβ::MYH11 fusion gene in acute lysis pneumopathy: A dual impact on risk and prognosis.

IF 3.8 2区 医学 Q1 HEMATOLOGY
Shuangwei Ying, Luxin Yang, Lulu Zhang, Ruimin Hong, Wenda Luo, Yanping Shao, Jie Sun, Qunyi Guo, Yi Luo
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引用次数: 0

Abstract

Acute lysis pneumopathy (ALP) is a rare but fatal complication that can occur during induction chemotherapy for newly diagnosed acute myeloid leukaemia (AML). Currently, there is a paucity of large case reports detailing high-risk and poor prognostic factors associated with its occurrence. To provide evidence-based guidance on ALP, we conducted a retrospective analysis of 608 patients with newly diagnosed AML (non-M3), among whom 20 developed ALP during hydroxycarbamide (hydroxyurea) therapy and/or induction chemotherapy, resulting in an overall incidence rate of 3.3% (20/608) and a mortality rate of 35% (7/20). Multivariable logistic regression revealed that male (odds ratio [OR] 5.852, 95% confidence interval [CI]: 1.006-34.028, p = 0.049), elevated leucocyte counts (OR 1.125, 95% CI: 1.050-1.205, p = 0.001) and CBFβ::MYH11 fusion positivity (OR 13.821, 95% CI: 3.002-63.634, p = 0.001) were independent risk factors for the occurrence of ALP. Notably, CBFβ::MYH11 fusion positivity was associated with improved survival in ALP patients (p = 0.015). This study provides preliminary insights into the risk and prognostic factors of ALP.

CBFβ::MYH11融合基因在急性溶解性肺病中的作用:对风险和预后的双重影响
急性溶解性肺病(ALP)是一种罕见但致命的并发症,可发生在新诊断的急性髓性白血病(AML)诱导化疗期间。目前,缺乏详细描述与其发生相关的高风险和预后不良因素的大型病例报告。为了提供ALP的循证指导,我们对608例新诊断的AML(非m3)患者进行了回顾性分析,其中20例患者在羟基脲治疗和/或诱导化疗期间发生ALP,总发病率为3.3%(20/608),死亡率为35%(7/20)。多变量logistic回归分析显示,男性(优势比[OR] 5.852, 95%可信区间[CI]: 1.006 ~ 34.028, p = 0.049)、白细胞计数升高(OR 1.125, 95% CI: 1.050 ~ 1.205, p = 0.001)和CBFβ::MYH11融合阳性(OR 13.821, 95% CI: 3.002 ~ 63.634, p = 0.001)是发生ALP的独立危险因素。值得注意的是,CBFβ::MYH11融合阳性与ALP患者的生存率提高相关(p = 0.015)。本研究对ALP的危险因素和预后因素提供了初步的认识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
8.60
自引率
4.60%
发文量
565
审稿时长
1 months
期刊介绍: The British Journal of Haematology publishes original research papers in clinical, laboratory and experimental haematology. The Journal also features annotations, reviews, short reports, images in haematology and Letters to the Editor.
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