急性淋巴细胞白血病急性淋巴细胞白血病
Hiroto Inaba1, Mel Greaves, Charles G Mullighan
1Department of Oncology, St Jude Children's Research Hospital and University of Tennessee Health Science Center, Memphis, TN 38105, USA. hiroto.inaba@stjude.org
Lancet (London, England)
|March 26, 2013
概括
儿童急性淋巴细胞白血病的存活率现在是90%,但新的遗传见解对于改善婴儿和成人的结果至关重要. 个性化医疗为更好的治疗和减少副作用提供了希望.
科学领域:
- 在瘤学瘤学.
- 遗传学 是一个遗传学.
- 儿科血液学/瘤学
背景情况:
- 急性淋巴细胞白血病 (ALL) 是一种常见的儿童癌症,原因多重.
- 儿科ALL的存活率显著改善,在临床试验中达到约90%.
- 然而,对于ALL的婴儿和成年人来说,预后仍然很差,需要创新的治疗策略.
研究的目的:
- 审查目前对ALL病变发生,治疗进展和未来方向的理解.
- 突出基因分析在识别新亚型和治疗点方面的作用.
- 强调需要新的方法来提高生存率和减少不良影响,特别是在高风险群体.
主要方法:
- 关于急性淋巴细胞白血病流行病学,治疗和遗传学的现有文献的综述.
- 对儿科ALL的生存数据和风险分层策略的分析.
- 讨论全基因组分析技术,用于识别白血病细胞中的遗传变化.
主要成果:
- 由于风险分层,个性化治疗修改 (药理动力学和药理基因组学) 以及增强的支持性护理,儿童ALL生存率有所改善.
- 全基因组DNA分析揭示了新的遗传变化,有助于白血病发生和定义新的疾病亚型.
- 这些遗传发现为个性化医学提供了潜在的预后标志物和治疗点.
结论:
- 虽然儿科ALL的存活率很高,但需要进一步的进展,特别是对于婴儿和成年人.
- 基因分析对理解ALL的复杂性和开发有针对性的疗法至关重要.
- 个性化医疗方法有望改善治疗结果并尽量减少ALL治疗中的毒性.
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