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急性白血病婴儿的表现敏锐度、诱导死亡率和资源利用。

Presentation acuity, induction mortality, and resource utilization in infants with acute leukemia.

机构信息

Department of Pediatrics and Adolescent Medicine, Einstein Healthcare Network Philadelphia, Philadelphia, Pennsylvania, USA.

Division of AIBMT, Department of Pediatrics, UCSF Benioff Children's Hospital, San Francisco, California, USA.

出版信息

Pediatr Blood Cancer. 2021 Jul;68(7):e28940. doi: 10.1002/pbc.28940. Epub 2021 Mar 11.

DOI:10.1002/pbc.28940
PMID:33704911
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8283996/
Abstract

BACKGROUND

Treatment of infants with acute leukemia remains challenging, especially for acute lymphocytic leukemia (ALL). Infants have shown markedly higher rates of induction mortality compared with noninfants. There are limited data on presentation acuity and supportive care utilization in this age group.

METHODS

In retrospective analyses of patients treated for new onset ALL or acute myeloid leukemia (AML) at pediatric hospitals contributing to the Pediatric Health Information System, we compared presentation acuity, induction mortality, and resource utilization in infants relative to noninfants less than 10 years at diagnosis.

RESULTS

Analyses included 10 359 children with ALL (405 infants, 9954 noninfants) and 871 AML (189 infants, 682 noninfants). Infants were more likely to present with multisystem organ failure compared to noninfants for both ALL (12% and 1%, PR = 10.8, 95% CI: 7.4, 15.7) and AML (6% vs. 3%; PR = 2.0, 95% CI: 1.0, 3.7). Infants with ALL had higher induction mortality compared to noninfants, even after accounting for differences in anthracycline exposure and presentation acuity (2.7% vs. 0.5%, HR = 2.1, 95% CI: 1.0, 4.8). Conversely, infants and noninfants with AML had similar rates of induction mortality (3.2% vs. 2.1%, HR = 1.2, 95% CI: 0.3, 3.9), which were comparable to rates among infants with ALL. Infants with ALL and AML had greater requirements for blood products, diuretics, supplemental oxygen, and ventilation during induction relative to noninfants.

CONCLUSIONS

Infants with leukemia present with higher acuity compared with noninfants. Induction mortality and supportive care requirements for infants with ALL were similar to all children with AML, and significantly higher than those for noninfants with ALL.

摘要

背景

婴儿急性白血病的治疗仍然具有挑战性,尤其是急性淋巴细胞白血病(ALL)。与非婴儿相比,婴儿的诱导死亡率明显更高。在这个年龄段,关于表现的紧迫性和支持性护理的利用的数据有限。

方法

在对参与儿科健康信息系统的儿科医院中治疗新发 ALL 或急性髓细胞白血病(AML)的患者进行回顾性分析中,我们比较了婴儿与诊断时小于 10 岁的非婴儿的表现紧迫性、诱导死亡率和资源利用。

结果

分析包括 10359 例 ALL(405 例婴儿,9954 例非婴儿)和 871 例 AML(189 例婴儿,682 例非婴儿)。与非婴儿相比,ALL(12%与 1%,PR=10.8,95%CI:7.4,15.7)和 AML(6%与 3%;PR=2.0,95%CI:1.0,3.7)患儿更有可能出现多系统器官衰竭。即使考虑到蒽环类药物暴露和表现紧迫性的差异,ALL 婴儿的诱导死亡率也高于非婴儿(2.7%与 0.5%,HR=2.1,95%CI:1.0,4.8)。相反,AML 婴儿和非婴儿的诱导死亡率相似(3.2%与 2.1%,HR=1.2,95%CI:0.3,3.9),与 ALL 婴儿的死亡率相当。ALL 和 AML 婴儿在诱导期间对血液制品、利尿剂、补充氧气和通气的需求大于非婴儿。

结论

与非婴儿相比,患有白血病的婴儿表现出更高的紧迫性。ALL 婴儿的诱导死亡率和支持性护理需求与所有 AML 儿童相似,明显高于 ALL 非婴儿。

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本文引用的文献

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Outcome of Infants Younger Than 1 Year With Acute Lymphoblastic Leukemia Treated With the Interfant-06 Protocol: Results From an International Phase III Randomized Study.《国际多中心 III 期随机研究:婴儿急性淋巴细胞白血病采用 Interfant-06 方案治疗的结局》
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How I treat infant leukemia.我如何治疗婴儿白血病。
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Gemtuzumab ozogamicin in infants with AML: results from the Children's Oncology Group trials AAML03P1 and AAML0531.吉妥珠单抗奥唑米星用于急性髓系白血病婴儿患者:儿童肿瘤协作组试验AAML03P1和AAML0531的结果
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Supportive care utilization and treatment toxicity in children with Down syndrome and acute lymphoid leukaemia at free-standing paediatric hospitals in the United States.美国独立儿科医院中唐氏综合征合并急性淋巴细胞白血病患儿的支持性护理利用情况及治疗毒性
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Infectious Complications in Children With Acute Myeloid Leukemia and Down Syndrome: Analysis of the Prospective Multicenter Trial AML-BFM 2004.急性髓系白血病合并唐氏综合征患儿的感染并发症:前瞻性多中心试验AML-BFM 2004分析
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Decreased induction morbidity and mortality following modification to induction therapy in infants with acute lymphoblastic leukemia enrolled on AALL0631: a report from the Children's Oncology Group.在 AALL0631 方案中,对急性淋巴细胞白血病婴儿诱导治疗进行改良后,诱导期发病率和死亡率降低:来自儿童肿瘤学组的报告。
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Intensified chemotherapy without SCT in infant ALL: results from COG P9407 (Cohort 3).无 SCT 强化化疗治疗婴儿 ALL:COG P9407(队列 3)的结果。
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Treatment of infant leukemias: challenge and promise.婴儿白血病的治疗:挑战与希望。
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