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采用剂量调整的6-巯基嘌呤对特发性肺含铁血黄素沉着症进行维持治疗。

Maintenance therapy with dose-adjusted 6-mercaptopurine in idiopathic pulmonary hemosiderosis.

作者信息

Luo Xue-Qun, Ke Zhi-Yong, Huang Li-Bin, Guan Xiao-Qing, Zhang Xiao-Li, Zhu Jia, Zhang Ying-Chuang

机构信息

Department of Pediatric, The First Affiliated Hospital of Sun Yat-Sen University, Zhongshan Er Lu, Guangzhou 510080, China.

出版信息

Pediatr Pulmonol. 2008 Nov;43(11):1067-1071. doi: 10.1002/ppul.20894.

Abstract

There are challenges for diagnosis and treatment of idiopathic pulmonary hemosiderosis (IPH). This clinical trial was to review the diagnosis and evaluate the efficacy of maintenance therapy with dose-adjusted 6-mercaptopurine (6MP) in IPH children. Fifteen children were enrolled. Prednisone was administered at 2 mg/kg/day for 4 weeks in acute phase of the disease followed by taper. 6MP was also started at 60 mg/m(2)/day simultaneously and continued for 3 years in outpatient. The delay in diagnosis of IPH is common and probably due to a lack of classical triad of IPH in most children. All the patients exhibited response to the initial treatment. Only one of eight patients with relative leukopenia on 6MP maintenance recurred while 5 of 7 others recurred (P < 0.05) during median 4.5-year follow-up. Of the latter five patients who recurred, 4 remained recurrence-free after adjusting the dose of 6MP upwards to keep relative leucopenia. It suggests that children with IPH could achieve steroid-free long term remission on 6MP maintenance therapy, and relative leukopenia on 6MP might be a simple maker of predicting clinical response in most IPH children.

摘要

特发性肺含铁血黄素沉着症(IPH)的诊断和治疗存在挑战。这项临床试验旨在回顾IPH患儿的诊断情况,并评估剂量调整后的6-巯基嘌呤(6MP)维持治疗的疗效。共纳入15名儿童。在疾病急性期,泼尼松以2mg/kg/天的剂量给药4周,随后逐渐减量。6MP也同时以60mg/m²/天的剂量开始给药,并在门诊持续使用3年。IPH诊断延迟很常见,可能是由于大多数儿童缺乏IPH的典型三联征。所有患者对初始治疗均有反应。在中位4.5年的随访期间,8名接受6MP维持治疗且有相对白细胞减少的患者中只有1例复发,而其他7名患者中有5例复发(P<0.05)。在后5例复发的患者中,4例在向上调整6MP剂量以维持相对白细胞减少后未再复发。这表明IPH患儿在6MP维持治疗下可实现无类固醇的长期缓解,并且6MP诱导的相对白细胞减少可能是大多数IPH患儿预测临床反应的一个简单指标。

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