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儿童急性早幼粒细胞白血病的感染:来自加拿大急性髓细胞白血病感染研究组。

Infections in pediatric acute promyelocytic leukemia: from the Canadian infections in acute myeloid leukemia research group.

出版信息

BMC Cancer. 2013 Jun 4;13:276. doi: 10.1186/1471-2407-13-276.

Abstract

BACKGROUND

It is not known whether children with acute promyelocytic leukemia (APL) have an infection risk similar to non- APL acute myeloid leukemia. The objective was to describe infectious risk in children with newly diagnosed APL and to describe factors associated with these infections.

METHODS

We conducted a retrospective, population-based cohort study that included children ≤ 18 years of age with de novo APL treated at 15 Canadian centers. Thirty-three children with APL were included; 78.8% were treated with APL -specific protocols.

RESULTS

Bacterial sterile site infection occurred in 12 (36.4%) and fungal sterile site infection occurred in 2 (6.1%) children. Of the 127 chemotherapy courses, 101 (79.5%) were classified as intensive and among these, the proportion in which a sterile site microbiologically documented infection occurred was 14/101 (13.9%). There was one infection-related death.

CONCLUSIONS

One third of children with APL experienced at least one sterile site bacterial infection throughout treatment and 14% of intensive chemotherapy courses were associated with a microbiologically documented sterile site infection. Infection rates in pediatric APL may be lower compared to non- APL acute myeloid leukemia although these children may still benefit from aggressive supportive care during intensive chemotherapy.

摘要

背景

目前尚不清楚患有急性早幼粒细胞白血病(APL)的儿童是否存在与非 APL 急性髓细胞白血病相似的感染风险。本研究旨在描述新诊断为 APL 的儿童的感染风险,并描述与这些感染相关的因素。

方法

我们进行了一项回顾性、基于人群的队列研究,纳入了在加拿大 15 个中心接受治疗的 15 岁以下初诊 APL 儿童患者。共纳入了 33 例 APL 患儿,其中 78.8%的患儿接受了 APL 特异性方案治疗。

结果

12 例(36.4%)患儿发生无菌部位细菌感染,2 例(6.1%)患儿发生无菌部位真菌感染。在 127 个化疗疗程中,101 个(79.5%)被归类为强化治疗,其中 13.9%(14/101)的无菌部位发生了微生物学证实的感染。有 1 例与感染相关的死亡。

结论

在整个治疗过程中,三分之一的 APL 患儿至少发生了一次无菌部位细菌感染,14%的强化化疗疗程与微生物学证实的无菌部位感染相关。与非 APL 急性髓细胞白血病相比,儿科 APL 的感染率可能较低,但这些患儿在强化化疗期间仍可能受益于积极的支持性护理。

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