低风险骨髓增生异常综合征的发病率和负担:一项全国人口研究。

IF 2.7 4区 医学 Q2 HEMATOLOGY
Maud D'Aveni, Jérôme Fernandes, Mélanie Chartier, François-Emery Cotté, Nicolas Pagès, Arnaud Panes, Aurélie Schmidt, Léa Webert, Thibault Comont
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引用次数: 0

摘要

背景:骨髓增生异常综合征(MDS)是一种主要影响老年人的血液系统恶性肿瘤,常导致贫血,严重影响生活质量。到目前为止,低风险MDS (LR-MDS)的治疗通常包括促红细胞生成素(ESA)作为一线治疗,在ESA耐药的情况下输血是必要的。本研究旨在利用法国国家健康数据系统(SNDS)评估法国LR-MDS患者的发病率、患病率和临床结局。材料与方法:对2018年至2022年期间接受治疗的822例LR-MDS患者进行回顾性队列分析,并根据患者的输血依赖进行分类。结果:结果显示,法国每年的中位LR-MDS外推发病率为5850例(每10万人中有6.9至9.3例)。输血依赖(TD)患者占队列的32.5%。输注依赖患者的2年总生存率为53%,而非输注依赖(NTD)患者的2年总生存率为70%。在研究期间,267例新治疗的LR-MDS患者中有41.9% (N = 112)死亡。此外,有88例死亡事件(无进展),26例估计进展为HR-MDS, 11例进展为急性髓系白血病。结论:这些发现强调了输血依赖对低密度mds患者的巨大负担,强调了改进治疗策略的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Incidence and Burden of Lower-Risk Myelodysplastic Syndrome: A Nationwide Population Study.

Background: Myelodysplastic syndromes (MDS) are hematological malignancies that primarily affect older individuals, often leading to anemia, which significantly impacts quality of life. Until now, the management of lower-risk MDS (LR-MDS) typically includes erythropoiesis-stimulating agents (ESAs) as first-line treatment, with transfusions becoming necessary in cases of ESA resistance. This study aimed to assess the incidence, prevalence, and clinical outcomes of LR-MDS patients in France, using the French National Health Data System (SNDS).

Materials and methods: A retrospective cohort of 822 LR-MDS patients treated between 2018 and 2022 was analyzed, with patients classified based on transfusion dependency.

Results: Results showed a median LR-MDS extrapolated incidence of 5,850 patients per year in France (between 6.9 to 9.3 cases per 100,000 persons). Transfusion-dependent (TD) patients represented 32.5% of the cohort. TD patients had a significantly lower 2-year overall survival rate of 53% compared to 70% in nontransfusion-dependent (NTD) patients. Over the study period, 41.9% (N = 112) died out of 267 newly treated LR-MDS patients. Also, there were 88 events of death (with no progression), 26 estimated progression to HR-MDS and 11 progression to acute myeloid leukemia.

Conclusion: These findings highlight the substantial burden of transfusion dependency in LR-MDS patients, emphasizing the need for improved therapeutic strategies.

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来源期刊
CiteScore
2.70
自引率
3.70%
发文量
1606
审稿时长
26 days
期刊介绍: Clinical Lymphoma, Myeloma & Leukemia is a peer-reviewed monthly journal that publishes original articles describing various aspects of clinical and translational research of lymphoma, myeloma and leukemia. Clinical Lymphoma, Myeloma & Leukemia is devoted to articles on detection, diagnosis, prevention, and treatment of lymphoma, myeloma, leukemia and related disorders including macroglobulinemia, amyloidosis, and plasma-cell dyscrasias. The main emphasis is on recent scientific developments in all areas related to lymphoma, myeloma and leukemia. Specific areas of interest include clinical research and mechanistic approaches; drug sensitivity and resistance; gene and antisense therapy; pathology, markers, and prognostic indicators; chemoprevention strategies; multimodality therapy; and integration of various approaches.
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