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皮下注射戈利木单抗诱导并维持生物制剂治疗抵抗的儿童溃疡性结肠炎暴发性发作的临床缓解:一例报告。

Subcutaneous golimumab induced and maintained clinical response in a child with a biological-experienced steroid-refractory flare of ulcerative colitis: A case report.

机构信息

Gastroenterology Department, Damascus Hospital, Damascus, Syria.

出版信息

Medicine (Baltimore). 2021 Sep 24;100(38):e27283. doi: 10.1097/MD.0000000000027283.

DOI:10.1097/MD.0000000000027283
PMID:34559136
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8462589/
Abstract

INTRODUCTION

Golimumab is a fully human antitumor necrosis monoclonal antibody that can be administered by either subcutaneous injection or intravenous infusion. Golimumab is approved for the treatment of the adults with rheumatic diseases, and ulcerative colitis, Whereas in children, golimumab is indicated only for the treatment of active polyarticular juvenile idiopathic arthritis. We have written on the off-label use of subcutaneous golimumab, which helped to induce and maintain remission on a low-weight biologically experienced child with steroid-refractory ulcerative colitis flare.

PATIENT CONCERNS

A 13-year-old pancolitis Syrian boy presented with abdominal pain and six to seven times bloody diarrhea. The child had treated with mesalamine 80 mg/kg/day, azathioprine 2.5 mg/kg/day, infliximab with an induction dose of 5 mg/kg at weeks 0, 2, and 6 followed by 5 mg/kg every 8 weeks. Infliximab did not maintain remission as the patient suffered from two flares that required hospital admission, intravenous corticosteroids, and infliximab escalation. Initial tests disclosed leukocytosis, anemia, hypoalbuminemia, an elevation in C-reactive protein and fecal calprotectin. All Stool studies were negative including routine stool cultures, Clostridium difficile toxin, Escherichia coli O157:H7, Cryptosporidium, and microscopy for ova and parasites. A sigmoidoscopy revealed multiple large ulcerations and spontaneous bleeding, colon biopsies were negative for Clostridium difficile and Cytomegalovirus. Cyclosporine, tacrolimus, and adalimumab were unavailable in Syria. Child's parents opposed colectomy as a treatment option.

DIAGNOSIS

Ulcerative colitis flare.

INTERVENTIONS

A subcutaneous golimumab with a loading dose of 200 mg at week 0, followed by 100 mg at week 2, then 50 mg every 4 weeks.

OUTCOMES

The patient achieved clinical remission by week sixth and maintained the remission for the next 90 weeks. At the time of last evaluation, tests, including C-reactive protein and fecal calprotectin, were within normal limits, complete colonoscopy revealed erythema, edema, mucosal friability, loss of vascular patterns, and pseudo-polyps. The Pediatric Ulcerative Colitis Activity Index and Mayo scores were 5 and 2 points, respectively. No adverse events were documented.

CONCLUSION

Golimumab has shown potential efficacy and safety in the treatment of ulcerative colitis in children which may indicate a significant future role for subcutaneous golimumab in pediatrics ulcerative colitis.

摘要

介绍

戈利木单抗是一种完全人源抗肿瘤坏死单克隆抗体,可通过皮下注射或静脉输注给药。戈利木单抗已获批准用于治疗成人风湿性疾病和溃疡性结肠炎,而在儿童中,戈利木单抗仅用于治疗活动型多发性幼年特发性关节炎。我们曾写过关于皮下注射戈利木单抗的超适应证使用,该方法有助于诱导和维持一名体重较轻、曾接受生物制剂治疗的儿童的缓解,该儿童患有类固醇难治性溃疡性结肠炎发作。

患者关注

一名 13 岁的叙利亚全结肠炎男孩出现腹痛和 6 至 7 次血性腹泻。该患儿曾接受美沙拉嗪 80mg/kg/天、硫唑嘌呤 2.5mg/kg/天、英夫利昔单抗诱导剂量 5mg/kg,分别在第 0、2 和 6 周,然后每 8 周 5mg/kg。英夫利昔单抗不能维持缓解,因为患儿经历了两次需要住院、静脉用皮质类固醇和英夫利昔单抗升级的发作。初始检查显示白细胞增多、贫血、低白蛋白血症、C 反应蛋白和粪便钙卫蛋白升高。所有粪便检查均为阴性,包括常规粪便培养、艰难梭菌毒素、大肠杆菌 O157:H7、隐孢子虫和粪便卵和寄生虫检查。乙状结肠镜检查显示多个大溃疡和自发性出血,结肠活检未见艰难梭菌和巨细胞病毒。环孢素、他克莫司和阿达木单抗在叙利亚不可用。患儿的父母反对将结肠切除术作为一种治疗选择。

诊断

溃疡性结肠炎发作。

干预措施

皮下注射戈利木单抗,第 0 周给予 200mg 负荷剂量,第 2 周给予 100mg,然后每 4 周给予 50mg。

结果

患者在第 6 周达到临床缓解,并在接下来的 90 周内保持缓解。在最后一次评估时,包括 C 反应蛋白和粪便钙卫蛋白在内的检查均在正常范围内,全结肠镜检查显示红斑、水肿、黏膜脆弱、血管模式丧失和假息肉。儿科溃疡性结肠炎活动指数和 Mayo 评分分别为 5 分和 2 分。无不良事件记录。

结论

戈利木单抗在儿童溃疡性结肠炎的治疗中显示出潜在的疗效和安全性,这可能表明皮下注射戈利木单抗在儿科溃疡性结肠炎中具有重要的未来作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c7a/8462589/c9cc3d26550d/medi-100-e27283-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c7a/8462589/d60c26afaadb/medi-100-e27283-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c7a/8462589/c9cc3d26550d/medi-100-e27283-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c7a/8462589/d60c26afaadb/medi-100-e27283-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c7a/8462589/c9cc3d26550d/medi-100-e27283-g002.jpg

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