A predictive model for therapy failure in chronic myeloid leukemia patients receiving tyrosine kinase inhibitor therapy

医学 伊马替尼 髓系白血病 酪氨酸激酶抑制剂 内科学 甲磺酸伊马替尼 肿瘤科 接收机工作特性 酪氨酸激酶 癌症 受体
作者
Xiaoshuai Zhang,Bingcheng Liu,Jian Huang,Y L Zhang,Na Xu,Robert Peter Gale,Weiming Li,Xiaoli Liu,Huanling Zhu,Ling Pan,Yunfan Yang,Hai Lin,Xin Du,Rong Liang,Chunyan Chen,Xiaodong Wang,Guohui Li,Zhougang Liu,Yanqing Zhang,Zhenfang Liu
出处
期刊:Blood [American Society of Hematology]
卷期号:144 (18): 1951-1961 被引量:3
标识
DOI:10.1182/blood.2024024761
摘要

Abstract Although tyrosine kinase inhibitor (TKI) therapy has markedly improved the survival of people with chronic-phase chronic myeloid leukemia (CML), 20% to 30% of people still experienced therapy failure. Data from 1955 consecutive patients with chronic-phase CML diagnosed by the European LeukemiaNet recommendations from 1 center receiving initial imatinib or a second-generation (2G) TKI therapy were interrogated to develop a clinical prediction model for TKI-therapy failure. This model was subsequently validated in 3454 patients from 76 other centers. Using the predictive clinical covariates associated with TKI-therapy failure, we developed a model that stratified patients into low-, intermediate- and high-risk subgroups with significantly different cumulative incidences of therapy failure (P < .001). There was good discrimination and calibration in the external validation data set, and the performance was consistent with that of the training data set. Our model had the better prediction discrimination than the Sokal and European Treatment and Outcome Study long-term survival scores, with the greater time-dependent area under the receiver-operator characteristic curve values and a better ability to redefine the risk of therapy failure. Our model could help physicians estimate the likelihood of initial imatinib or 2G TKI–therapy failure in people with chronic-phase CML.
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