Department of Medicine, Massachusetts General Hospital (Division of Gastroenterology), Harvard University, Boston, MA, USA.
Department of Medicine (Division of Gastroenterology) and Farncombe Family Digestive Health Research Institute, McMaster University, Hamilton, ON, Canada.
Eur J Gastroenterol Hepatol. 2024 Jun 1;36(6):704-711. doi: 10.1097/MEG.0000000000002759. Epub 2024 Mar 22.
Vedolizumab is a first-line treatment option for ulcerative colitis. There are differences in incidence of ulcerative colitis between males and females, but whether sex affects treatment outcomes is less clear. We examined sex-based differences in patients with ulcerative colitis initiated on vedolizumab from two major randomized controlled trials (RCTs). We conducted a post-hoc analysis on participants with ulcerative colitis from the VARSITY and GEMINI-1 RCTs who received vedolizumab. Outcomes of interest were rates of clinical improvement, clinical remission, and endoscopic improvement at weeks 6, 14, and 52 in male and female participants, as were differences in concentrations of trough vedolizumab and C-reactive protein; 1009 persons in GEMINI-1 and VARSITY trials were included. Male and female patients had similar disease characteristics aside from males being more likely to have Mayo 3 grade endoscopic severity at baseline (62.8 vs. 48.9%, P < 0.001). At week 6, females were more likely to have endoscopic improvement (47.4 vs. 35.2%, P = 0.001) and increased vedolizumab trough levels [34.0 (23.0-44.5) vs. 28.9 (19.0-34.6), P < 0.001]. The probability of achieving clinical remission (28.9 vs. 34.5%, P = 0.057) or endoscopic improvement (35.5 vs. 39.3%, P = 0.212) at week 52 was not different between males and females. Females with ulcerative colitis treated with vedolizumab appear more likely to achieve early endoscopic improvement than males, though longer-term outcomes demonstrated no difference. Further studies are required to better understand mechanisms through which sex or sex-associated factors could influence response to therapy in ulcerative colitis.
维得利珠单抗是溃疡性结肠炎的一线治疗选择。溃疡性结肠炎在男性和女性中的发病率存在差异,但性别是否影响治疗效果尚不清楚。我们研究了两项主要随机对照试验(RCT)中接受维得利珠单抗治疗的溃疡性结肠炎患者的性别差异。我们对 VARSITY 和 GEMINI-1 RCT 中接受维得利珠单抗治疗的溃疡性结肠炎患者进行了事后分析。主要观察指标为治疗第 6、14 和 52 周时男性和女性患者临床缓解、临床缓解和内镜改善的比例,以及维得利珠单抗谷浓度和 C 反应蛋白的差异;GEMINI-1 和 VARSITY 两项试验共纳入 1009 例患者。除男性基线时内镜严重程度更可能为 Mayo 3 级(62.8%比 48.9%,P<0.001)外,男性和女性患者的疾病特征相似。第 6 周时,女性内镜改善的可能性更高(47.4%比 35.2%,P=0.001),维得利珠单抗谷浓度更高[34.0(23.0-44.5)比 28.9(19.0-34.6),P<0.001]。第 52 周时,男性和女性患者达到临床缓解(28.9%比 34.5%,P=0.057)或内镜改善(35.5%比 39.3%,P=0.212)的概率无差异。与男性相比,接受维得利珠单抗治疗的女性溃疡性结肠炎患者更有可能早期获得内镜改善,但长期结局无差异。需要进一步研究以更好地了解性别或与性别相关的因素如何影响溃疡性结肠炎的治疗反应机制。