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爱尔兰唐氏综合征儿童中髓系白血病的回顾性研究。

A retrospective study of myeloid leukaemia in children with Down syndrome in Ireland.

机构信息

Royal College of Surgeons in Ireland, Dublin, Ireland.

Department of Haematology and Oncology, Children's Health Ireland at Crumlin, Dublin, Ireland.

出版信息

Ir J Med Sci. 2020 Aug;189(3):979-984. doi: 10.1007/s11845-020-02181-y. Epub 2020 Jan 31.

Abstract

BACKGROUND

Acute megakaryoblastic leukaemia (AMKL) is a subtype of myeloid leukaemia and is the most common leukaemia type in children with Down syndrome (DS) under 4 years of age. AMKL is often preceded by a transient neonatal pre-leukaemic syndrome, transient myeloproliferative disorder (TMD). Although TMD often spontaneously resolves, 20-30% of these patients subsequently develop AMKL within the first 4 years of life.

AIMS

To perform a retrospective consecutive national audit of all documented cases of childhood TMD and AMKL-DS from 1990 to 2018 at Our Lady's Children's Hospital, Crumlin (OLCHC), Ireland.

METHODS

All patients with a diagnosis of AMKL treated consecutively at (OLCHC) between 1990 and 2018 were reviewed. Kaplan-Meier survival curves were constructed.

RESULTS

Twenty-seven patients with AMKL-DS were identified. A prior neonatal diagnosis of TMD was described in 10 patients (37%). Nineteen patients (70%) are alive and well, in complete remission, at a median follow-up of 11.4 years. Overall survival (OS) of this cohort has risen from 54% from those treated between the years 1990 and 2004 (n = 13) to 93% for those treated between the years 2005 and 2018 (n = 14).

CONCLUSION

High cure rates are observed in AMKL-DS using current polychemotherapy protocols. The finding of a low platelet count at time of diagnosis is in keeping with the knowledge that AMKL-DS is a malignancy of platelet progenitor cells.

摘要

背景

急性巨核细胞白血病(AMKL)是髓系白血病的一种亚型,是 4 岁以下唐氏综合征(DS)儿童中最常见的白血病类型。AMKL 通常在前一过性新生儿白血病前期综合征、一过性骨髓增生异常(TMD)之后发生。虽然 TMD 通常会自发消退,但这些患者中有 20-30%会在生命的头 4 年内随后发展为 AMKL。

目的

对 1990 年至 2018 年在爱尔兰克里姆林(OLCHC)圣母儿童医院记录的所有儿童 TMD 和 AMKL-DS 病例进行回顾性连续国家审计。

方法

回顾了 1990 年至 2018 年期间(OLCHC)连续治疗的所有 AMKL 患者。绘制了 Kaplan-Meier 生存曲线。

结果

确定了 27 例 AMKL-DS 患者。在 10 例患者(37%)中描述了新生儿期 TMD 的诊断。19 例患者(70%)存活且情况良好,完全缓解,中位随访时间为 11.4 年。该队列的总体生存率(OS)从 1990 年至 2004 年(n=13)治疗的 54%上升至 2005 年至 2018 年(n=14)治疗的 93%。

结论

使用当前多化疗方案,在 AMKL-DS 中观察到高治愈率。诊断时血小板计数低的发现与 AMKL-DS 是血小板祖细胞恶性肿瘤的知识相符。

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