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Dasatinib as first-line treatment for adult patients with Philadelphia chromosome-positive acute lymphoblastic leukemia.达沙替尼作为费城染色体阳性急性淋巴细胞白血病成人患者的一线治疗药物。
Blood. 2011 Dec 15;118(25):6521-8. doi: 10.1182/blood-2011-05-351403. Epub 2011 Sep 19.
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Modern therapy of acute lymphoblastic leukemia.急性淋巴细胞白血病的现代治疗。
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Genetic variegation of clonal architecture and propagating cells in leukaemia.白血病克隆结构和增殖细胞的遗传异质性。
Nature. 2011 Jan 20;469(7330):356-61. doi: 10.1038/nature09650. Epub 2010 Dec 15.
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Chemotherapy-phased imatinib pulses improve long-term outcome of adult patients with Philadelphia chromosome-positive acute lymphoblastic leukemia: Northern Italy Leukemia Group protocol 09/00.化疗相伊马替尼脉冲改善费城染色体阳性成人急性淋巴细胞白血病患者的长期预后:意大利北部白血病组方案 09/00。
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Acquisition of genome-wide copy number alterations in monozygotic twins with acute lymphoblastic leukemia.同卵双胞胎急性淋巴细胞白血病中获得全基因组拷贝数改变。
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Gene expression profiling-based dissection of MLL translocated and MLL germline acute lymphoblastic leukemia in infants.基于基因表达谱分析的婴儿中 MLL 易位型和 MLL 胚系急性淋巴细胞白血病。
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Early T-cell precursor leukaemia: a subtype of very high-risk acute lymphoblastic leukaemia.早期T细胞前体白血病:一种极高危急性淋巴细胞白血病亚型。
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Deletion of IKZF1 and prognosis in acute lymphoblastic leukemia.IKZF1缺失与急性淋巴细胞白血病的预后
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Pediatric-inspired therapy in adults with Philadelphia chromosome-negative acute lymphoblastic leukemia: the GRAALL-2003 study.针对费城染色体阴性成人急性淋巴细胞白血病的儿童启发式疗法:GRAALL - 2003研究
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Cytogenetics of paediatric and adolescent acute lymphoblastic leukaemia.儿童及青少年急性淋巴细胞白血病的细胞遗传学
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5202 例意大利 AIEOP 和 GIMEMA 方案中急性淋巴细胞白血病患者的临床生物学特征,并按年龄队列分层。

Clinico-biological features of 5202 patients with acute lymphoblastic leukemia enrolled in the Italian AIEOP and GIMEMA protocols and stratified in age cohorts.

出版信息

Haematologica. 2013 Nov;98(11):1702-10. doi: 10.3324/haematol.2012.080432. Epub 2013 May 28.

DOI:10.3324/haematol.2012.080432
PMID:23716539
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3815170/
Abstract

The outcome of children and adults with acute lymphoblastic leukemia is markedly different. Since there is limited information on the distribution of clinico-biological variables in different age cohorts, we analyzed 5202 patients with acute lymphoblastic leukemia enrolled in the Italian multicenter AIEOP and GIMEMA protocols and stratified them in nine age cohorts. The highest prevalence of acute lymphoblastic leukemia was observed in children, although a second peak was recorded from the 4(th) decade onwards. Interestingly, the lowest incidence was found in females between 14-40 years. Immunophenotypic characterization showed a B-lineage in 85.8% of patients: a pro-B stage, associated with MLL/AF4 positivity, was more frequent in patients between 10-50 years. T-lineage leukemia (14.2%) was rare among small children and increased in patients aged 10-40 years. The prevalence of the BCR/ABL1 rearrangement increased progressively with age starting from the cohort of patients 10-14 years old and was present in 52.7% of cases in the 6th decade. Similarly, the MLL/AF4 rearrangement constantly increased up to the 5(th) decade, while the ETV6/RUNX1 rearrangement disappeared from the age of 30 onwards. This study shows that acute lymphoblastic leukemia in adolescents and young adults is characterized by a male prevalence, higher percentage of T-lineage cases, an increase of poor prognostic molecular markers with aging compared to cases in children, and conclusively quantified the progressive increase of BCR/ABL(+) cases with age, which are potentially manageable by targeted therapies.

摘要

儿童和成人急性淋巴细胞白血病的预后明显不同。由于关于不同年龄组临床生物学变量分布的信息有限,我们分析了意大利多中心 AIEOP 和 GIMEMA 方案中纳入的 5202 例急性淋巴细胞白血病患者,并将其分为 9 个年龄组。尽管在第四十年龄段以后记录到第二个高峰,但儿童中急性淋巴细胞白血病的发病率最高。有趣的是,在 14-40 岁之间的女性中发现发病率最低。免疫表型特征显示 85.8%的患者为 B 细胞谱系:10-50 岁患者中更常见前 B 期,与 MLL/AF4 阳性相关。T 细胞白血病(14.2%)在幼儿中罕见,在 10-40 岁患者中增加。BCR/ABL1 重排的发生率随着年龄的增长而逐渐增加,从 10-14 岁的患者组开始,并在第六十年龄组中存在于 52.7%的病例中。同样,MLL/AF4 重排持续增加到第五十年龄组,而 ETV6/RUNX1 重排从 30 岁开始消失。这项研究表明,青少年和年轻成人的急性淋巴细胞白血病以男性患病率较高、T 细胞谱系病例比例较高、与儿童病例相比,预后不良的分子标志物随年龄增加而增加为特征,并且明确地量化了 BCR/ABL(+)病例随年龄增加的逐渐增加,这些病例可以通过靶向治疗进行有效管理。