干细胞治疗儿童不良AML的不同方面:什么时候HSCT是最好的答案?

B. Gustafsson
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引用次数: 0

摘要

儿童急性髓性白血病是一种具有不同形态学和细胞遗传学特征的异质性疾病。新的诊断工具和治疗方法,改进的支持性护理以及在选择造血干细胞移植(HSCT)供体时使用基因组组织分型增加了生存率。首次完全缓解的HSCT的候选者是细胞遗传学或分子预后不良标记的患者,或首次诱导后细胞增殖率为15%的患者。最小残留疾病的使用也可以识别首次完全缓解的HSCT受益儿童和HSCT后复发迹象的患者。急性髓系白血病的预后和治愈率仍然很差,需要评估新的诊断工具和治疗策略。在这个管理的角度,未来的管理新的最小残留疾病的工具进行了讨论,调理疗法,以及不同的移植程序,包括单倍体移植和单倍体相同的移植。
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Different aspects of stem cell procedures in children with poor responding AML: when is HSCT the best answer?
Acute myeloid leukemia in children is a heterogeneous disease with different morphological and cytogenetic features. New diagnostic tools and treatments, improved supportive care and the use of genomic tissue typing in selecting donors for hematopoietic stem cell transplantation (HSCT) adds to increased survival rates. Candidates to HSCT in first complete remission are patients with cytogenetic or molecular unfavorable prognostic markers, or blasts >15% after first induction. The use of minimal residual disease can also identify children benefiting from HSCT in first complete remission and the patients post HSCT with signs of relapse. The outcome and cure rate of acute myeloid leukemia, still remains poor and new diagnostic tools and treatments strategies need to be evaluated. In this management perspective, future management of novel minimal residual disease tools are discussed, conditioning therapies, as well as different transplantation procedures including haplo-transplantation and haplo-identical nat...
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期刊介绍: International Journal of Hematologic Oncology welcomes unsolicited article proposals. Email us today to discuss the suitability of your research and our options for authors, including Accelerated Publication. Find out more about publishing open access with us here.
期刊最新文献
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