Department of Hematology and Oncology, Fondazione Istituto di Ricovero e Cura a Carattere Scientifico Policlinico S. Matteo, and.
Blood. 2013 Oct 24;122(17):2943-64. doi: 10.1182/blood-2013-03-492884. Epub 2013 Aug 26.
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 with a poor 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 because of advanced 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.
在欧洲白血病网的骨髓增生异常综合征(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。对文献进行了系统评价,包括索引原始论文、索引综述和教育论文,以及会议论文集的摘要。指南是根据一组面向患者和治疗的问题制定的,建议根据证据支持水平进行制定和排序。MDS 应根据 2008 年世界卫生组织标准进行分类。准确的风险评估不仅需要评估与疾病相关的因素,还需要评估与血液以外的合并症相关的因素。对个体风险的评估可以识别预后不良但适合进行强化治疗的患者,主要是异基因干细胞移植。由于年龄较大和/或存在临床相关合并症和较差的功能状态,许多 MDS 患者不符合潜在的治愈性治疗的条件。在这些患者中,治疗干预的目的是预防与细胞减少相关的发病率并维持生活质量。正在开发许多新的药物,但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。