儿童急性髓性白血病的长期生存结果:泰国(一个资源有限的国家)43 年的经验。

IF 2.2 4区 医学 Q3 HEMATOLOGY
Pornpun Sripornsawan, Shevachut Chavananon, Sirinthip Kittivisuit, Natsaruth Songthawee, Edward B McNeil, Thirachit Chotsampancharoen
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引用次数: 0

摘要

尽管发达国家在治疗急性髓性白血病(AML)儿童患者方面取得了进步,但中低收入国家的治疗效果仍然不佳。本研究旨在调查在泰国一家三级医疗中心接受治疗的急性髓细胞白血病患儿的治疗效果。我们根据采用的化疗方案将研究分为 4 个研究阶段。1-4期的5年无事件生存概率(pEFS)分别为19.0%、20.6%、17.4%和37.3%(P值=0.32),而5年总生存概率(pOS)分别为19.0%、24.7%、18.7%和42.5%(P值=0.18)。多变量模型显示,第 1 期和第 4 期的 5 年总生存率有所提高(p 值 = 0.04)。年龄、白细胞计数和研究时期是生存结果的重要预测因素。随着时间的推移,急性髓细胞白血病患者的 pOS 有所提高,从 19.0% 提高到 42.5%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Long-term survival outcome of childhood acute myeloid leukemia: a 43-year experience in Thailand, a resource-limited country.

Although there have been advances in treating pediatric patients with acute myeloid leukemia (AML) in developed countries, outcomes in low- to middle-income countries remain poor. The goal of this study was to investigate the outcomes in children with AML who were treated at a tertiary care center in Thailand. We divided the study into 4 research periods based on the chemotherapy protocols employed. The 5-year probabilities of event-free survival (pEFS) rates for periods 1-4 were 19.0%, 20.6%, 17.4%, and 37.3% (p value = 0.32), while the 5-year probabilities of overall survival (pOS) rates were 19.0%, 24.7%, 18.7%, and 42.5% (p value = 0.18), respectively. The multivariable model indicated an improvement in 5-year pOS between periods 1 and 4 (p value = 0.04). Age, white blood cell count, and study period were significant predictors of survival outcomes. The pOS of AML patients improved over time, increasing from 19.0% to 42.5%.

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来源期刊
Leukemia & Lymphoma
Leukemia & Lymphoma 医学-血液学
CiteScore
4.10
自引率
3.80%
发文量
384
审稿时长
1.8 months
期刊介绍: Leukemia & Lymphoma in its fourth decade continues to provide an international forum for publication of high quality clinical, translational, and basic science research, and original observations relating to all aspects of hematological malignancies. The scope ranges from clinical and clinico-pathological investigations to fundamental research in disease biology, mechanisms of action of novel agents, development of combination chemotherapy, pharmacology and pharmacogenomics as well as ethics and epidemiology. Submissions of unique clinical observations or confirmatory studies are considered and published as Letters to the Editor
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