O'Connor Anthony, Marples Maria, Mulatero Clive, Hamlin John, Ford Alexander C
Leeds Gastroenterology Institute, Bexley Wing, St. James's University Hospital, Beckett Street, Leeds LS9 7TF, UK.
St James's Institute of Oncology, St. James's University Hospital, Leeds, UK.
Therap Adv Gastroenterol. 2016 Jul;9(4):457-62. doi: 10.1177/1756283X16646709. Epub 2016 May 10.
Ipilimumab is an anticytotoxic T-lymphocyte antigen-4 (CTLA-4) monoclonal antibody used for the treatment of malignant melanoma. It can cause immune-mediated inflammatory adverse events, including diarrhoea and even intestinal perforation or death in clinical trials but there is a dearth of data on postmarketing outcomes.
A total of 546 patients attending for treatment of metastatic melanoma between 1 January 2009 and 31 August 2015 were identified by interrogation of the oncology database. A total of 83 of these patients received ipilimumab. Clinical information was extracted from chart reviews, endoscopy and radiology reports, and prescription data.
A total of 83 patients received ipilimumab. Only 19.3% (n = 16) of patients developed a diarrhoeal illness not attributable to other causes. The median grade of diarrhoea among included patients was 2 (range 1-4). In two cases, diarrhoea settled spontaneously without any specific treatment. A total of 87.5% of patients received antidiarrhoeal agents such as loperamide or codeine. These resolved symptoms in all patients with grade 1 diarrhoea. For other treatment, 50% patients received systemic glucocorticosteroids and 31.3% required infliximab. Infliximab resolved symptoms in 100% of cases compared with 50% for systemic glucocorticosteroids.
The rate of diarrhoea related to ipilimumab in real-world practice is substantial, but below the range observed in data from RCTs. Grade 1 colitis can usually be managed symptomatically, without recourse to stopping ipilimumab. When diarrhoea was grade 2 or above, results from glucocorticosteroids use proved disappointing; but infliximab has been shown to work well. Further research is required into the earlier use of infliximab as an effective treatment for ipilimumab-induced diarrhoea.
伊匹单抗是一种抗细胞毒性T淋巴细胞抗原4(CTLA-4)单克隆抗体,用于治疗恶性黑色素瘤。在临床试验中,它可引起免疫介导的炎症性不良事件,包括腹泻,甚至肠道穿孔或死亡,但关于上市后结果的数据却很匮乏。
通过查询肿瘤数据库,确定了2009年1月1日至2015年8月31日期间共546例接受转移性黑色素瘤治疗的患者。其中共有83例患者接受了伊匹单抗治疗。临床信息从病历审查、内镜检查和放射学报告以及处方数据中提取。
共有83例患者接受了伊匹单抗治疗。只有19.3%(n = 16)的患者出现了非其他原因所致的腹泻疾病。纳入患者中腹泻的中位分级为2级(范围1 - 4级)。有两例腹泻未经任何特殊治疗自行缓解。共有87.5%的患者接受了止泻药物,如洛哌丁胺或可待因。这些药物使所有1级腹泻患者的症状得到缓解。对于其他治疗,50%的患者接受了全身性糖皮质激素治疗,31.3%的患者需要英夫利昔单抗治疗。英夫利昔单抗使100%的病例症状得到缓解,而全身性糖皮质激素治疗的缓解率为50%。
在实际临床实践中,与伊匹单抗相关的腹泻发生率较高,但低于随机对照试验数据中观察到的范围。1级结肠炎通常可通过对症治疗,无需停用伊匹单抗。当腹泻为2级或以上时,使用糖皮质激素的效果令人失望;但英夫利昔单抗已显示出良好的疗效。需要进一步研究更早使用英夫利昔单抗作为伊匹单抗诱导腹泻的有效治疗方法。