Division of Hematology, Department of Medicine, Mayo Clinic, Rochester, MN.
Department of Hematology, Center for the Study of Myelofibrosis, IRCCS Policlinico S Matteo Foundation, Pavia, Italy.
Blood. 2024 Oct 24;144(17):1813-1820. doi: 10.1182/blood.2024025802.
With emerging new drugs in myelofibrosis (MF), a robust and harmonized framework for defining the severity of anemia and response to treatment will enhance clinical investigation and facilitate interstudy comparisons. Accordingly, the lead authors on the 2013 edition of the International Working Group-European LeukemiaNet (IWG-ELN) response criteria in MF were summoned to revise their document with the intent to (1) account for gender-specific differences in determining hemoglobin levels for eligibility criteria; (2) revise the definition of transfusion-dependent anemia (TDA) based on current restrictive transfusion practices; and (3) provide a structurally simple and easy to apply response criteria that are sensitive enough to detect efficacy signals (minor response) and also account for major responses. The initial draft of the 2024 IWG-ELN proposed criteria was subsequently circulated around a wider group of international experts and their feedback incorporated. The proposed articles include new definitions for TDA (≥3 units in the 12 weeks before study enrollment) and hemoglobin thresholds for eligibility criteria (<10 g/dL for women and <11 g/dL for men). The revised document also provides separate (TDA vs non-TDA) and graded (major vs minor response) response criteria while preserving the requirement for a 12-week period of screening and observation on treatment.
随着骨髓纤维化(MF)领域新药物的不断涌现,建立一个强大且协调一致的贫血严重程度和治疗反应定义框架,将有助于加强临床研究并促进研究间的比较。因此,召集了 2013 年版国际工作组-欧洲白血病网络(IWG-ELN)MF 反应标准的主要作者对其文件进行修订,旨在:(1)考虑到确定资格标准时血红蛋白水平的性别差异;(2)根据当前限制性输血实践修订输血依赖型贫血(TDA)的定义;(3)提供一种结构简单、易于应用的反应标准,该标准具有足够的敏感性以检测疗效信号(轻微反应),并考虑到主要反应。随后,2024 年 IWG-ELN 建议标准的初始草案在更广泛的国际专家群体中进行了传阅,并纳入了他们的反馈意见。拟议的条款包括 TDA 的新定义(在研究入组前 12 周内≥3 单位)和资格标准的血红蛋白阈值(女性<10g/dL,男性<11g/dL)。修订后的文件还提供了单独的(TDA 与非 TDA)和分级的(主要与轻微反应)反应标准,同时保留了 12 周的筛选和治疗观察期要求。