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首页> 外文期刊>Blood: The Journal of the American Society of Hematology >Diagnosis and treatment of primary myelodysplastic syndromes in adults: Recommendations from the European LeukemiaNet
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Diagnosis and treatment of primary myelodysplastic syndromes in adults: Recommendations from the European LeukemiaNet

机译:成人原发性骨髓增生异常综合症的诊断和治疗:欧洲白血病网的建议

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Within the myelodysplastic syndrome (MDS) work package of the European LeukemiaNet, an Expert Panel was selected according to the framework elements of the National Institutes of Health Consensus Development Program. A systematic review of the literature was performed that included indexed original papers, indexed reviews and educational papers, and abstracts of conference proceedings. Guidelines were developed on the basis of a list of patient- and therapy-oriented questions, and recommendations were formulated and ranked according to the supporting level of evidence. MDSs should be classified according to the 2008 World Health Organization criteria. An accurate risk assessment requires the evaluation of not only disease-related factors but also of those related to extrahematologic comorbidity. The assessment of individual risk enables the identification of fit patients withapoor prognosis who are candidates for up-front intensive treatments, primarily allogeneic stem cell transplantation. A high proportion of MDS patients are not eligible for potentially curative treatment becauseofadvanced age and/or clinically relevant comorbidities and poor performance status. In these patients, the therapeutic intervention is aimed at preventing cytopenia-related morbidity and preserving quality of life. A number of new agents are being developed for which the available evidence is not sufficient to recommend routine use. The inclusion of patients into prospective clinical trials is strongly recommended.
机译:在欧洲白血病网的骨髓增生异常综合症(MDS)工作包中,根据美国国立卫生研究院共识发展计划的框架要素选择了一个专家小组。对文献进行了系统的审查,其中包括索引原始论文,索引评论和教育论文以及会议记录摘要。根据一系列针对患者和治疗的问题制定了指南,并根据证据的支持水平制定了建议并进行了排名。 MDS应根据2008年世界卫生组织的标准进行分类。准确的风险评估不仅需要评估与疾病相关的因素,还需要评估与血液外合并症相关的因素。对个体风险的评估可以确定预后较差的适合患者,这些患者适合进行预先强化治疗,主要是异基因干细胞移植。由于年龄和/或临床相关合并症的高发和不良的表现,很大比例的MDS患者不符合潜在治疗的条件。在这些患者中,治疗干预旨在预防与血细胞减少症相关的发病,并保持生活质量。正在开发许多新药,其现有证据不足以推荐常规使用。强烈建议将患者纳入前瞻性临床试验。

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