Leitch Heather A, Buckstein Rena, Zhu Nancy, Nevill Thomas J, Yee Karen W L, Leber Brian, Keating Mary-Margaret, St Hilaire Eve, Kumar Rajat, Delage Robert, Geddes Michelle, Storring John M, Shamy April, Elemary Mohamed, Wells Richard A
Hematology, St. Paul's Hospital and the University of British Columbia, Vancouver, BC, Canada.
Odette Cancer Centre, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada.
Leuk Res. 2018 Nov;74:21-41. doi: 10.1016/j.leukres.2018.09.005. Epub 2018 Sep 19.
In 2008 the first evidence-based Canadian consensus guideline addressing the diagnosis, monitoring and management of transfusional iron overload in patients with myelodysplastic syndromes (MDS) was published. The Canadian Consortium on MDS, comprised of hematologists from across Canada with a clinical and academic interest in MDS, reconvened to update these guidelines. A literature search was updated in 2017; topics reviewed include mechanisms of iron overload induced cellular damage, evidence for clinical endpoints impacted by iron overload including organ dysfunction, infections, marrow failure, overall survival, acute myeloid leukemia progression, and endpoints around hematopoietic stem-cell transplant. Evidence for an impact of iron reduction on the same endpoints is discussed, guidelines are updated, and areas identified where evidence is suboptimal. The guidelines address common questions around the diagnosis, workup and management of iron overload in clinical practice, and take the approach of who, when, why and how to treat iron overload in MDS. Practical recommendations for treatment and monitoring are made. Evidence levels and grading of recommendations are provided for all clinical endpoints examined.
2008年,首部基于证据的加拿大共识指南发布,该指南涉及骨髓增生异常综合征(MDS)患者输血性铁过载的诊断、监测及管理。由加拿大各地对MDS有临床及学术兴趣的血液学家组成的加拿大MDS联盟再次召开会议以更新这些指南。2017年更新了文献检索;所审查的主题包括铁过载诱导细胞损伤的机制、铁过载影响临床终点的证据,这些临床终点包括器官功能障碍、感染、骨髓衰竭、总生存期、急性髓系白血病进展以及造血干细胞移植相关终点。讨论了铁减少对相同终点影响的证据,更新了指南,并确定了证据不足的领域。这些指南解决了临床实践中有关铁过载诊断、检查及管理的常见问题,并采用了针对MDS中铁过载治疗的对象、时间、原因及方式的方法。给出了治疗及监测的实用建议。为所有审查的临床终点提供了证据水平及推荐分级。