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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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单位: [1]Shandong Univ, Qilu Hosp, Dept Hematol, Jinan, Shandong, Peoples R China [2]Chinese Acad Med Sci, Inst Hematol, Tianjin, Peoples R China [3]Chinese Acad Med Sci, Blood Dis Hosp, Tianjin, Peoples R China [4]Peking Union Med Coll, Tianjin, Peoples R China [5]Fujian Med Univ Union Hosp, Fujian Inst Hematol, Fujian Prov Key Lab Hematol, Fuzhou, Fujian, Peoples R China [6]Soochow Univ, Jiangsu Inst Hematol, Affiliated Hosp 1, Key Lab Thrombosis & Hemostasis,Minist Hlth, Suzhou, Jiangsu, Peoples R China [7]Zhejiang Univ, Affiliated Hosp 1, Dept Hematol, Coll Med, Hangzhou, Zhejiang, Peoples R China [8]Sichuan Univ, West China Hosp, Dept Hematol, Chengdu, Sichuan, Peoples R China [9]Huazhong Univ Sci & Technol, Tongji Hosp, Tongji Med Coll, Dept Hematol, Wuhan, Hubei, Peoples R China [10]Huazhong Univ Sci & Technol, Union Hosp, Tongji Med Coll, Inst Hematol, Wuhan, Hubei, Peoples R China [11]Peking Univ, Inst Hematol, Peoples Hosp, Beijing, Peoples R 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[2017]版:
大类 | 2 区 医学
小类 | 2 区 肿瘤学
最新[2025]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[2016]版:
Q1 ONCOLOGY
最新[2024]版:
Q1 HEMATOLOGY Q1 ONCOLOGY

影响因子: 最新[2024版] 最新五年平均 出版当年[2016版] 出版当年五年平均 出版前一年[2015版] 出版后一年[2017版]

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第一作者单位: [1]Shandong Univ, Qilu Hosp, Dept Hematol, Jinan, Shandong, Peoples R China
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