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首页> 外文期刊>Pediatric blood & cancer >Stage at diagnosis for children with blood cancers in Australia: Application of the Toronto Paediatric Cancer Stage Guidelines in a population‐based national childhood cancer registry
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Stage at diagnosis for children with blood cancers in Australia: Application of the Toronto Paediatric Cancer Stage Guidelines in a population‐based national childhood cancer registry

机译:澳大利亚血癌儿童诊断的阶段:在基于人群的全国儿童癌症登记处的多伦多小儿癌症阶段指南的应用

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Abstract Background Information on stage at diagnosis for childhood blood cancers is essential for surveillance but is not available on a population basis in most countries. Our aim was to apply the internationally endorsed Toronto Paediatric Cancer Stage Guidelines to children (15 years) with acute lymphoblastic leukemia (ALL), acute myeloid leukemia (AML), Hodgkin lymphoma (HL), or non‐Hodgkin lymphoma (NHL) and to assess differences in survival by stage at diagnosis. Procedure Stage was defined by extent of involvement of the central nervous system (CNS) for ALL and AML and using the Ann Arbor and St Jude‐Murphy systems for HL and NHL, respectively. The study cohort was drawn from the population‐based Australian Childhood Cancer Registry, consisting of children diagnosed with one of these four blood cancers between 2006 and 2014 with follow‐up to 2015. Five‐year observed survival was estimated from the Kaplan–Meier method. Results Stage was assigned to 2201 of 2351 eligible patients (94%), ranging from 85% for AML to 95% for ALL, HL, and NHL. Survival following ALL varied from 94% (95% CI?=?93%–95%) for CNS1 disease to 89% (95% CI?=?79%–94%) for CNS2 ( P ?=?0.07), whereas for AML there was essentially no difference in survival between CNS ? (77%) and CNS + disease (78%; P ?=?0.94). Nearly all children with HL survived for five years. There was a trend ( P ?=?0.04) toward worsening survival with higher stage for NHL. Conclusions These results provide the first population‐wide picture of the distribution and outcomes for childhood blood cancers in Australia by extent of disease at diagnosis and provide a baseline for future comparisons.
机译:在诊断童年血癌舞台上抽象的背景资料是用于监控必不可少的,但不可用在大多数国家人口的基础上。我们的目标是在国际认可的多伦多儿童癌症分期指南适用于儿童(小于15岁)急性淋巴细胞白血病(ALL),急性髓系白血病(AML),霍奇金淋巴瘤(HL)和非霍奇金淋巴瘤(NHL)并通过在阶段诊断评估存活差异。过程阶段通过用于ALL和AML的中枢神经系统(CNS)的参与程度,并使用分别用于HL和非霍奇金淋巴瘤,安阿伯和St犹大书-墨菲系统定义。该研究组从基于人口的澳大利亚儿童癌症登记处绘制,由诊断为2006年至2014年间这四种血液癌症之一随访至2015年五年生存率观察孩子从Kaplan-Meier方法估计。结果阶段被分配到2201的2351周符合条件的患者(94%),范围从85%到AML 95%ALL,HL,和非霍奇金淋巴瘤。生存遵循所有从94%(95%CI =?93%-95%),用于CNS1疾病变化,以89%(95%CI =?79%-94%)为CNS2(P = 0.07),而对于AML有中枢神经系统之间的生存本质上没有区别? (77%)和CNS疾病+(78%; P = 0.94?)。几乎与所有HL孩子生存了五年。有朝与NHL更高的阶段不断恶化的生存趋势(P?=?0.04)。结论:这些结果提供了诊断在澳大利亚的分布和成果童年血癌的疾病程度的第一群体的图形,并且为今后的比较提供了一个基准。

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