Xu Qiushi, Jin Lixin, Ou Chengzhu, Xu Tianming, Yang Zhuo, Zhang Runfeng, Liu Shuang, Yan Xuemin, Ruan Gechong, Li Ji, Li Jingnan
Department of Gastroenterology, Chinese Academy of Medical Sciences, Peking Union Medical College Hospital, No.1 Shuaifuyuan Wangfujing Dongcheng District, Beijing, 100730, China.
Department of Gastroenterology, People's Hospital of Rizhao, Rizhao, 276800, China.
BMC Pharmacol Toxicol. 2024 Dec 18;25(1):96. doi: 10.1186/s40360-024-00825-8.
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.
To examine the efficacy and safety of azathioprine (AZA) in CCS patients.
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.
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.
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.
克朗凯特-加拿大综合征(CCS)是一种罕见的非遗传性慢性炎症性疾病,其特征为胃肠道息肉和外胚层异常。皮质类固醇疗法是CCS的主要治疗药物。少数研究表明,免疫抑制剂可能是类固醇难治性、类固醇依赖性或不耐受患者的选择。
探讨硫唑嘌呤(AZA)治疗CCS患者的疗效和安全性。
我们回顾性分析了2014年7月至2023年10月期间接受硫唑嘌呤治疗的12例CCS患者的病历,并收集和分析了包括人口统计学特征、治疗方案和不良事件在内的临床资料。还对11例患者采用桑格测序法回顾性评估了TPMT和NUDT15基因的遗传变异。
所有患者基线时均处于活动期,9例(75%)患者联合使用皮质类固醇。根据适应证,6例患者为类固醇依赖性或不耐受,另外6例患者需要强化治疗。AZA的目标剂量为每天1.0至1.5mg/kg。10例(83.3%)患者获得临床缓解,其中3例内镜缓解,5例内镜改善。3例(25%)患者分别发生卡氏肺孢子虫肺炎、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例患者中鉴定出TPMT和NUDT15的4种杂合错义变异。1例携带TPMT*6且每天服用2.04mg/kg剂量AZA的患者发生严重白细胞减少。
硫唑嘌呤可能是类固醇依赖性或不耐受、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,尤其是骨髓抑制,治疗前检测TPMT和NUDT15基因型可能有助于用药指导。