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Early BCR-ABL1 decline in imatinib-treated patients with chronic myeloid leukemia: results from a multicenter study of the Chinese CML alliance

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机构: [1]Department of Hematology, Qilu Hospital, Shandong University, Jinan,Shandong, China [2]Institute of Hematology and Blood Diseases Hospital,Chinese Academy of Medical Sciences and Peking Union Medical College,Tianjin, China [3]Fujian Provincial Key Laboratory of Hematology, Fujian Instituteof Hematology, Fujian Medical University Union Hospital, Fuzhou, Fujian,China [4]Jiangsu Institute of Hematology, Key Laboratory of Thrombosis andHemostasis of Ministry of Health, The First Affiliated Hospital of SoochowUniversity, Suzhou, Jiangsu, China [5]Department of Hematology, The FirstAffiliated Hospital, Zhejiang University College of Medicine, Hangzhou,Zhejiang, China [6]Department of Hematology, West China Hospital, SichuanUniversity, Chengdu, Sichuan, China [7]Department of Hematology, TongjiHospital, Tongji Medical College, Huazhong University of Science andTechnology, Wuhan, Hubei, China [8]Institute of Hematology, Union Hospital,Tongji Medical College, Huazhong University of Science and Technology,Wuhan, Hubei, China [9]Institute of Hematology, Peking University People’sHospital, Beijing, China
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An early molecular response is spectacularly predictive of outcome in chronic myeloid leukemia (CML) and early response landmarks may identify the high-risk patients likely to be benefit from an early therapy switch. In this study, we evaluated the most relevant cutoffs for early molecular response markers (BCR-ABL1 values at 3 months, log reduction and halving time between diagnosis and 3 months) in 476 first-line imatinib-treated Chinese patients with chronic phase CML. All outcomes were significantly superior for the 324 patients with 3-month BCR-ABL1 <= 10%, so did for the 270 patients with BCR-ABL1 >0.61 log reduction. BCR-ABL1 halving time <= 22 days was identified for patients with the most favorable outcome. Moreover, the prognosis was significantly poorest for patients with both halving time >44 days and BCR-ABL1 >10%. Importantly, multivariate regression analysis demonstrated that a BCR-ABL1 log reduction calculated at 3 months of 0.61 was the only variable that significantly predicted for OS. Our results highlight the importance of rapid initial decline of BCR-ABL1 in predicting satisfactory outcome. Our data support the evidence that monitoring BCR-ABL1 values at an early time point could contribute to accurately assess response and ultimately guide clinical decisions regarding the timing of therapeutic intervention.

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出版当年[2018]版:
大类 | 1 区 医学
小类 | 2 区 肿瘤学
最新[2023]版:
大类 | 1 区 医学
小类 | 1 区 血液学 1 区 肿瘤学
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出版当年[2018]版:
Q1 HEMATOLOGY Q1 ONCOLOGY
最新[2023]版:
Q1 HEMATOLOGY Q1 ONCOLOGY

影响因子: 最新[2023版] 最新五年平均 出版当年[2018版] 出版当年五年平均 出版前一年[2017版] 出版后一年[2019版]

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第一作者机构: [1]Department of Hematology, Qilu Hospital, Shandong University, Jinan,Shandong, China
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