Lie Mitchell R K L, Paulides Emma, van der Woude C Janneke
Department of Gastroenterology and Hepatology, Erasmus MC, Rotterdam, The Netherlands.
Int J Colorectal Dis. 2020 Aug;35(8):1489-1500. doi: 10.1007/s00384-020-03663-2. Epub 2020 Jun 26.
Biological therapies are currently the mainstay in the treatment of patients with inflammatory bowel diseases (IBD). Several factors are known to influence the efficacy and tolerability of biologicals, such as CRP levels or previous biological use. Whether patient sex affects the efficacy or tolerability is unclear but would help with better risk and benefit stratification. This systematic review assesses patient sex on the efficacy and tolerability of biological therapies in IBD patients.
A systematic literature review was performed using Embase (including MEDLINE), MEDLINE OvidSP, Cochrane Central Register of Controlled Trials, Web of Science and PubMed. The primary outcome was the influence of patient sex on endoscopic outcomes in IBD patients treated with biologicals. The secondary outcome was the influence of patient sex on adverse events. Studies were included in the assessment regardless of study type or setting.
The search yielded 19,461 citations; after review, 55 studies were included in the study, involving 28,465 patients treated with adalimumab, certolizumab pegol, infliximab, or vedolizumab. There was no significant association between patient sex and endoscopic efficacy in 41 relevant studies. Increased adverse events were associated with female sex in 7 out of 14 relevant studies.
There is no evidence for a sex difference in endoscopically measured response to biological therapies in IBD patients. However, there is an influence of sex on the occurrence of adverse events.
生物疗法目前是炎症性肠病(IBD)患者治疗的主要手段。已知有几个因素会影响生物制剂的疗效和耐受性,如CRP水平或既往生物制剂使用情况。患者性别是否会影响疗效或耐受性尚不清楚,但这将有助于更好地进行风险和获益分层。本系统评价评估了患者性别对IBD患者生物疗法疗效和耐受性的影响。
使用Embase(包括MEDLINE)、MEDLINE OvidSP、Cochrane对照试验中央注册库、科学网和PubMed进行系统文献综述。主要结局是患者性别对接受生物制剂治疗的IBD患者内镜检查结果的影响。次要结局是患者性别对不良事件的影响。无论研究类型或背景如何,研究均纳入评估。
检索得到19461条引文;经审查,55项研究纳入本研究,涉及28465例接受阿达木单抗、赛妥珠单抗、英夫利昔单抗或维多珠单抗治疗的患者。在41项相关研究中,患者性别与内镜疗效之间无显著关联。在14项相关研究中的7项中,不良事件增加与女性性别相关。
没有证据表明IBD患者对生物疗法的内镜测量反应存在性别差异。然而,性别对不良事件的发生有影响。