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首页> 外文期刊>Blood: The Journal of the American Society of Hematology >How I treat newly diagnosed T-cell acute lymphoblastic leukemia and T-cell lymphoblastic lymphoma in children
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How I treat newly diagnosed T-cell acute lymphoblastic leukemia and T-cell lymphoblastic lymphoma in children

机译:如何治疗新诊断的T细胞急性淋巴细胞白血病和儿童T细胞淋巴细胞淋巴瘤

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摘要

T-cell acute lymphoblastic leukemia (T-ALL) is an aggressive malignancy that has historically been associated with a very poor prognosis. Nevertheless, despite a lack of incorporation of novel agents, the development of intensified T-ALL-focused protocols has resulted in significant improvements in outcome in children. Through the use of several representative cases, we highlight the key changes that have driven these advances including asparaginase intensification, the use of induction dexamethasone, and the safe omission of cranial radiotherapy. We discuss the results of recent trials to explore key topics including the implementation of risk stratification with minimal residual disease measurement and how to treat high-risk subtypes such as early T-cell precursor ALL. In particular, we address current discrepancies in treatment between different cooperative groups, including the use of nelarabine, and provide rationales for current treatment protocols for both T-ALL and T-lymphoblastic lymphoma.
机译:T细胞急性淋巴细胞白血病(T-all)是一种历史上有关的侵略性恶性肿瘤,其预后非常差。尽管如此,尽管缺乏新型药剂的融合,但加强的T-全以各种协议的发展导致了儿童结果的显着改善。通过使用多种代表性的案例,我们突出了推动这些进步的关键变化,包括天冬酰胺酶强化,使用诱导地塞米松以及颅放射的安全遗漏。我们讨论最近试验的结果,以探索关键主题,包括实施风险分层,具有最小的残留疾病测量以及如何治疗高风险亚型,例如早期T细胞前驱患者。特别是,我们解决了不同协作组之间治疗的当前差异,包括使用Nelarabine,并为T-全淋巴细胞淋巴瘤提供当前治疗方案的理由。

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