University Hospital Mannheim, Heidelberg University, Mannheim, Germany.
Spanish Network on Mastocytosis, Toledo and Salamanca, Spain.
J Clin Oncol. 2019 Nov 1;37(31):2846-2856. doi: 10.1200/JCO.19.00640. Epub 2019 Sep 11.
To develop a risk score for patients with advanced systemic mastocytosis (AdvSM) that integrates clinical and mutation characteristics.
The study included 383 patients with AdvSM from the German Registry on Disorders of Eosinophils and Mast Cells (training set; n = 231) and several centers for mastocytosis in the United States and Europe, all within the European Competence Network on Mastocytosis (validation set; n = 152). A Cox multivariable model was used to select variables that were predictive of overall survival (OS).
In multivariable analysis, the following risk factors were identified as being associated with OS: age greater than 60 years, anemia (hemoglobin < 10 g/dL), thrombocytopenia (platelets < 100 × 10/L), presence of one high molecular risk gene mutation (ie, in , , and/or ), and presence of two or more high molecular risk gene mutations. By assigning hazard ratio-weighted points to these variables, the following three risk categories were defined: low risk (median OS, not reached), intermediate risk (median OS, 3.9 years; 95% CI, 2.1 to 5.7 years), and high risk (median OS, 1.9 years; 95% CI, 1.3 to 2.6 years; < .001). The mutation-adjusted risk score (MARS) was independent of the WHO classification and was confirmed in the independent validation set. During a median follow-up time of 2.2 years (range, 0 to 23 years), 63 (16%) of 383 patients experienced a leukemic transformation to secondary mast cell leukemia (32%) or secondary acute myeloid leukemia (68%). The MARS was also predictive for leukemia-free survival ( < .001).
The MARS is a validated, five-parameter, WHO-independent prognostic score that defines three risk groups among patients with AdvSM and may improve up-front treatment stratification for these rare hematologic neoplasms.
开发一种适用于晚期系统性肥大细胞增多症(AdvSM)患者的风险评分,该评分整合了临床和突变特征。
该研究纳入了来自德国嗜酸性粒细胞和肥大细胞疾病登记处(训练集;n = 231)以及美国和欧洲多个肥大细胞疾病中心的 383 例 AdvSM 患者,所有患者均属于欧洲肥大细胞疾病网络(验证集;n = 152)。使用 Cox 多变量模型来选择与总生存(OS)相关的预测变量。
多变量分析确定了与 OS 相关的以下危险因素:年龄大于 60 岁、贫血(血红蛋白 < 10 g/dL)、血小板减少症(血小板 < 100×10/L)、存在 1 个高风险基因突变(即、和/或)、存在 2 个或更多高风险基因突变。通过为这些变量分配危害比加权点,定义了以下三个风险类别:低危(中位 OS,未达到)、中危(中位 OS,3.9 年;95%CI,2.1 至 5.7 年)和高危(中位 OS,1.9 年;95%CI,1.3 至 2.6 年;<0.001)。突变调整风险评分(MARS)独立于世界卫生组织(WHO)分类,并在独立验证集中得到证实。在中位随访时间 2.2 年(范围,0 至 23 年)期间,383 例患者中有 63 例(16%)发生白血病转化为继发性肥大细胞白血病(32%)或继发性急性髓系白血病(68%)。MARS 也预测白血病无进展生存(<0.001)。
MARS 是一种经过验证的、五参数、与 WHO 无关的预后评分,可在 AdvSM 患者中定义三个风险组,可能改善这些罕见血液肿瘤的初始治疗分层。