Division of Gastroenterology, Mount Sinai Hospital, University of Toronto, Ontario, Canada, Toronto, Ontario, Canada.
Zane Cohen Centre for Digestive Diseases, Mount Sinai Hospital, Toronto, Ontario, Canada.
Inflamm Bowel Dis. 2020 Apr 11;26(5):766-773. doi: 10.1093/ibd/izz199.
Golimumab is approved as a therapy for ulcerative colitis (UC) patients. Recent data also demonstrate efficacy in Crohn's disease (CD); however, little is known about target drug levels to achieve endoscopic remission.
We performed a retrospective analysis of IBD patients on maintenance golimumab. Median trough levels were compared using Kruskal-Wallis test, and logistic regression was used to construct a probabilistic model to determine sensitivity and specificity of levels predicting mucosal healing.
Fifty-eight patients on maintenance golimumab were included (n = 39 CD, n = 19 UC/IBD-unclassified [IBDU]). Forty percent (n = 23) were cotreated with an immunomodulator, 95% (n = 55) of patients were anti-TNF experienced, and 15.5% (n = 9) had 3 or more prior biologic therapies. Forty-four percent of patients achieved mucosal healing with endoscopic response in a further 26% of patients. Clinical remission was recorded in 41% of patients, and 82% had clinical response. Patients were treated with doses generally higher than the approved maintenance dose. In CD patients, median golimumab trough levels were higher in patients with mucosal healing (8.8 μg/mL vs 5.08 μg/mL, P = 0.03). After calculation of a receiver operating characteristic (ROC) curve for mucosal healing vs nonresponse, a trough level >8 μg/mL was associated with mucosal healing, with 67% sensitivity, 88% specificity, and a likelihood ratio of 3:4.
Treatment with golimumab was associated with mucosal healing in 44% of all IBD patients. Higher golimumab levels were associated with mucosal healing in CD. These findings support the need for prospective studies to determine target golimumab levels in IBD, which may impact current clinical practices in relation to selection of maintenance dosing.
戈利木单抗已被批准用于溃疡性结肠炎(UC)患者的治疗。最近的数据也表明其在克罗恩病(CD)中的疗效;然而,对于实现内镜缓解的目标药物水平知之甚少。
我们对接受维持性戈利木单抗治疗的 IBD 患者进行了回顾性分析。使用 Kruskal-Wallis 检验比较中位数谷浓度,并使用逻辑回归构建概率模型,以确定预测黏膜愈合的浓度的敏感性和特异性。
共纳入 58 例接受维持性戈利木单抗治疗的患者(n = 39 例 CD,n = 19 例 UC/IBD 未分类 [IBDU])。40%(n = 23)联合使用免疫调节剂,95%(n = 55)的患者为抗 TNF 经验丰富,15.5%(n = 9)有 3 种或更多种先前的生物治疗药物。44%的患者内镜缓解,进一步 26%的患者黏膜愈合。41%的患者记录临床缓解,82%的患者有临床反应。患者接受的剂量普遍高于批准的维持剂量。在 CD 患者中,黏膜愈合患者的戈利木单抗谷浓度中位数较高(8.8μg/mL 比 5.08μg/mL,P = 0.03)。在计算黏膜愈合与无反应的 ROC 曲线后,谷浓度>8μg/mL 与黏膜愈合相关,具有 67%的敏感性、88%的特异性和 3:4 的似然比。
戈利木单抗治疗与所有 IBD 患者中 44%的黏膜愈合相关。较高的戈利木单抗水平与 CD 中的黏膜愈合相关。这些发现支持需要进行前瞻性研究来确定 IBD 中的戈利木单抗目标水平,这可能会影响与维持剂量选择相关的当前临床实践。