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唐氏综合征患儿急性淋巴细胞白血病化疗的疗效与毒性

Outcome and toxicity of chemotherapy for acute lymphoblastic leukemia in children with Down syndrome.

作者信息

Shah Niketa, Al-Ahmari Ali, Al-Yamani Arwa, Dupuis Lee, Stephens Derek, Hitzler Johann

机构信息

Division of Hematology/Oncology, University of Toronto, Toronto, Ontario, Canada.

出版信息

Pediatr Blood Cancer. 2009 Jan;52(1):14-9. doi: 10.1002/pbc.21737.

Abstract

BACKGROUND

Acute lymphoblastic leukemia (ALL) in children with Down syndrome (DS) presents with an increased incidence, higher frequency of adverse effects and inferior probability of survival. Attempts at improving outcomes face the dilemma posed by the need to avoid excessive toxicity while maintaining the efficacy of treatment. Dose reductions and avoidance of infusions of intermediate and high-dose methotrexate are common in this group.

PROCEDURE

In a matched pair analysis we compared adverse effects and survival after ALL chemotherapy using intermediate and high doses of methotrexate in children with and without Down syndrome.

RESULTS

Following intermediate and high doses of methotrexate to treat primary ALL, children with DS did not require opiate analgesia and parenteral nutrition for severe mucositis more often than children without DS. Children with DS spent more days in hospital and missed more doses of maintenance chemotherapy. Chemotherapy dose reductions were common and in this study had no detectable adverse impact. Event-free and overall survival (OS) of children with ALL was lower in the DS than the non-Down syndrome (NDS) control group. The difference, however, was no longer significant during the recent treatment era.

CONCLUSIONS

The feasibility of all treatment elements that are efficacious in pediatric ALL needs to be carefully considered in children with DS. In addition to survival data, the prospective collection of data on both adverse events and treatment modifications is essential to strike a balance between the avoidance of adverse effects and the need for intensive therapy that will safely improve ALL outcomes in this group.

摘要

背景

唐氏综合征(DS)患儿的急性淋巴细胞白血病(ALL)发病率增加,不良反应发生率更高,生存概率更低。改善治疗结果的尝试面临着两难境地,即需要在避免过度毒性的同时保持治疗效果。在该群体中,减少剂量以及避免输注中高剂量甲氨蝶呤很常见。

方法

在一项配对分析中,我们比较了使用中高剂量甲氨蝶呤进行ALL化疗后,唐氏综合征患儿与非唐氏综合征患儿的不良反应和生存情况。

结果

在使用中高剂量甲氨蝶呤治疗原发性ALL后,唐氏综合征患儿因严重黏膜炎而需要阿片类镇痛和肠外营养的情况并不比非唐氏综合征患儿更常见。唐氏综合征患儿住院天数更多,错过的维持化疗剂量也更多。化疗剂量减少很常见,且在本研究中未发现有可检测到的不良影响。唐氏综合征患儿的无事件生存率和总生存率(OS)低于非唐氏综合征(NDS)对照组。然而,在最近的治疗时代,这种差异不再显著。

结论

对于唐氏综合征患儿,需要仔细考虑所有对小儿ALL有效的治疗要素的可行性。除了生存数据外,前瞻性收集不良事件和治疗调整数据对于在避免不良反应和进行强化治疗以安全改善该群体ALL治疗结果之间取得平衡至关重要。

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