年轻人
医学
入射(几何)
费城染色体
儿科
淋巴细胞白血病
肿瘤科
内科学
白血病
遗传学
生物
染色体易位
基因
物理
光学
作者
Ying‐Jung Huang,Hsi‐Che Liu,Ming‐Chung Kuo,Ting‐Chi Yeh,Tung‐Liang Lin,Shih‐Hsiang Chen,Tang-Her Jaing,Shih-Chung Wang,Te-Kau Chang,Hsiu‐Ju Yen,Jiunn‐Ming Sheen,Ming-Chung Wang,Tung‐Huei Lin,Ting‐Yu Huang,Hsiao‐Wen Kao,Che-Wei Ou,Yu‐Shin Hung,Chih‐Cheng Hsiao,Lee‐Yung Shih
摘要
Unconventional genetic subtypes of B-cell precursor acute lymphoblastic leukaemia (B-ALL) were analysed to compare their frequency and their impact on outcomes between children and young adults in Taiwan. Unconventional subtypes were found in 23.0% of 456 paediatric B-ALL and 24.5% of 139 young adult B-ALL. The most frequently unconventional subtype both in children and young adults was BCR::ABL1-like, which could be subdivided into different kinase-altering aberrations in 67.3% of children and 78.6% of young adults. CRLF2-R was more frequent in children, while IL7R mutations were more common in young adults. In children, favourable outcomes were observed in patients with DUX4-R and PAX5alt, whereas those with BCR::ABL1-like and MEF2D-R had inferior outcomes. BCR::ABL1-like and MEF2D-R were also the independent predictors of inferior event-free survival in children. Conversely, most unconventional subtypes in young adults were associated with adverse outcomes except for DUX4-R. We found a lower incidence of BCR::ABL1-like and a better prognosis for paediatric PAX5alt in Taiwan compared to the West. Additionally, genetic differences were identified between paediatric and young adult BCR::ABL1-like subtypes. The extremely poor prognosis for unclassified young adults highlights the potential use of further subdivision of unfavourable genetic subtypes in refining risk classification and treatment optimization.
科研通智能强力驱动
Strongly Powered by AbleSci AI