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Low CREBBP expression is associated with adverse long-term outcomes in paediatric acute lymphoblastic leukaemia

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机构: [1]Chinese Acad Med Sci, Inst Hematol, Tianjin, Peoples R China; [2]Chinese Acad Med Sci, Blood Dis Hosp, Tianjin, Peoples R China; [3]Peking Union Med Coll, Tianjin, Peoples R China; [4]Beijing Key Lab Pediat Hematol Oncol, Beijing, Peoples R China; [5]Minist Educ, Key Lab Major Dis Children, Beijing, Peoples R China; [6]Minist Educ, Natl Key Discipline Pediat, Beijing, Peoples R China; [7]Capital Med Univ, Beijing Childrens Hosp, Hematol & Oncol Ctr, Beijing, Peoples R China; [8]Capital Med Univ, Beijing Childrens Hosp, Beijing, Peoples R China
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关键词: acute lymphoblastic leukaemia clinical studies CREBBP paediatrics prognosis

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ObjectivesCREBBP alterations are associated with many diseases including leukaemia. However, CREBBP expression and its clinical relevance in paediatric acute lymphoblastic leukaemia have not been elucidated. MethodsWe studied CREBBP mRNA expression in 349 patients treated with either the BCH-2003 or CCLG-2008 protocol. Using a receiver operating characteristic curve, patients were divided into low- or high-CREBBP. The association among clinicobiological characteristics, outcomes and CREBBP level was analysed. ResultsLow expression of CREBBP (<1.0) at diagnosis was found in 97.7% of patients and increased significantly after complete remission. Low-CREBBP patients were associated with unfavourable clinical presentations, poor prednisone response and high minimal residual disease (>10(-2)) after induction. We found significantly poorer event-free survival (EFS) and overall survival (OS) in low-CREBBP group whether administered BCH-2003 or CCLG-2008. Low-CREBBP was an inferior independent prognostic factor in BCH-2003; patients with low-CREBBP had better outcomes on an intermediate-risk regimen than a standard-risk regimen involving the CCLG-2008 protocol. Patients stratified to high-risk with low-CREBBP had the worst EFS and OS. ConclusionsThese findings indicate that low-CREBBP is predictive of unfavourable outcomes; thus, a more intensive treatment protocol is necessitated for standard-risk patients with insufficient CREBBP and that a specific target therapy is necessitated for high-risk patients.

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出版当年[2016]版:
大类 | 3 区 医学
小类 | 4 区 血液学
最新[2023]版:
大类 | 3 区 医学
小类 | 3 区 血液学
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出版当年[2015]版:
Q3 HEMATOLOGY
最新[2023]版:
Q2 HEMATOLOGY

影响因子: 最新[2023版] 最新五年平均 出版当年[2015版] 出版当年五年平均 出版前一年[2014版] 出版后一年[2016版]

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第一作者机构: [1]Chinese Acad Med Sci, Inst Hematol, Tianjin, Peoples R China; [2]Chinese Acad Med Sci, Blood Dis Hosp, Tianjin, Peoples R China; [3]Peking Union Med Coll, Tianjin, Peoples R China; [4]Beijing Key Lab Pediat Hematol Oncol, Beijing, Peoples R China; [5]Minist Educ, Key Lab Major Dis Children, Beijing, Peoples R China; [6]Minist Educ, Natl Key Discipline Pediat, Beijing, Peoples R China; [7]Capital Med Univ, Beijing Childrens Hosp, Hematol & Oncol Ctr, Beijing, Peoples R China;
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通讯机构: [1]Chinese Acad Med Sci, Inst Hematol, Tianjin, Peoples R China; [2]Chinese Acad Med Sci, Blood Dis Hosp, Tianjin, Peoples R China; [3]Peking Union Med Coll, Tianjin, Peoples R China; [4]Beijing Key Lab Pediat Hematol Oncol, Beijing, Peoples R China; [5]Minist Educ, Key Lab Major Dis Children, Beijing, Peoples R China; [6]Minist Educ, Natl Key Discipline Pediat, Beijing, Peoples R China; [7]Capital Med Univ, Beijing Childrens Hosp, Hematol & Oncol Ctr, Beijing, Peoples R China; [8]Capital Med Univ, Beijing Childrens Hosp, Beijing, Peoples R China
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