硫唑嘌呤治疗cronkite - canada综合征的疗效和安全性:北京协和医院病例分析

IF 2.8 3区 医学 Q2 PHARMACOLOGY & PHARMACY BMC Pharmacology & Toxicology Pub Date : 2024-12-18 DOI:10.1186/s40360-024-00825-8
Qiushi Xu, Lixin Jin, Chengzhu Ou, Tianming Xu, Zhuo Yang, Runfeng Zhang, Shuang Liu, Xuemin Yan, Gechong Ruan, Ji Li, Jingnan Li
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引用次数: 0

摘要

背景:cronkwhite - canada综合征(CCS)是一种罕见的非遗传性慢性炎症性疾病,以胃肠道息肉和外胚层异常为特征。皮质类固醇治疗是治疗CCS的主要药物。很少有研究表明免疫抑制剂可能是类固醇难治性、类固醇依赖或不耐受患者的选择。目的:探讨硫唑嘌呤(azathiopine, AZA)治疗CCS患者的疗效和安全性。方法:回顾性分析2014年7月至2023年10月12例接受硫唑嘌呤治疗的CCS患者的临床资料,包括人口学特征、治疗方案和不良事件。对11例患者的TPMT和NUDT15基因的遗传变异也采用sanger测序进行回顾性评估。结果:所有患者基线时均处于活动期,9例患者(75%)联合使用皮质类固醇。由于适应症,6例患者类固醇依赖或不耐受,另有6例患者需要强化治疗。AZA的靶剂量为1.0 ~ 1.5 mg/kg / d。10例(83.3%)患者达到临床缓解,其中内镜缓解3例,内镜改善5例。3例(25%)患者分别出现卡氏肺囊虫肺炎、肝功能障碍和白细胞减少,导致在最初3个月内停用AZA。在4例患者中发现TPMT和NUDT15的4个杂合错义变异。1例TPMT*6患者,每天服用2.04 mg/kg剂量的AZA,出现严重白细胞减少。结论:硫唑嘌呤可能是类固醇依赖或不耐受或需要强化治疗的CCS患者的良好替代药物。应密切监测不良事件,特别是骨髓抑制,治疗前检测TPMT和NUDT15基因型可能有助于药物指导。
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Efficacy and safety of azathioprine in patients with Cronkhite-Canada syndrome: a case series from Peking Union Medical College Hospital.

Background: Cronkhite-Canada syndrome (CCS) is a rare non-hereditary chronic inflammatory disease characteristic of gastrointestinal polyps and ectodermal abnormalities. Corticosteroid therapy is the mainstay medication for CCS. Few studies indicated immunosuppressants might be the choices for patients with steroid refractory, steroid dependent or intolerant.

Aim: To examine the efficacy and safety of azathioprine (AZA) in CCS patients.

Method: We retrospectively reviewed the records of 12 CCS patients treated with azathioprine between July 2014 and October 2023 and the clinical data including demographic characteristics, treatment regimen and adverse events were subsequently collected and analyzed. The genetic variants of TPMT and NUDT15 genes were also retrospectively assessed using sanger sequencing in 11 patients.

Outcome: All patients were in active stage at baseline and 9 patients (75%) were in combination with corticosteroid. On account of the indication, 6 patients were steroid dependent or intolerant and another 6 patients needed augmentation therapy. The target dose of AZA was 1.0 to 1.5 mg/kg per day. Ten (83.3%) patients achieved clinical response, of whom 3 cases had endoscopic remission and 5 cases had endoscopic improvement respectively. Three (25%) patients suffered from pneumocystis carinii pneumonia, liver dysfunction and leukopenia, respectively, resulting in cessation of AZA in the initial 3 months. Four heterozygous missense variants of TPMT and NUDT15 were identified in four patients. One patient who had TPMT*6 and took AZA with the dose of 2.04 mg/kg per day suffered from severe leukopenia.

Conclusion: Azathioprine might be a good alternative medication in CCS patients who are steroid dependent or intolerant, or need augmentation therapy. The adverse events should be closely monitored especially myelosuppression and the tests of TPMT and NUDT15 genotypes before therapy may be helpful for medication guidance.

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来源期刊
BMC Pharmacology & Toxicology
BMC Pharmacology & Toxicology PHARMACOLOGY & PHARMACYTOXICOLOGY&nb-TOXICOLOGY
CiteScore
4.80
自引率
0.00%
发文量
87
审稿时长
12 weeks
期刊介绍: BMC Pharmacology and Toxicology is an open access, peer-reviewed journal that considers articles on all aspects of chemically defined therapeutic and toxic agents. The journal welcomes submissions from all fields of experimental and clinical pharmacology including clinical trials and toxicology.
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