Department of Medicine, Division of Gastroenterology and Farncombe Family Digestive Health Research Institute, McMaster University, Hamilton, Ontario, Canada.
Division of Gastroenterology, Northwestern University, Chicago, Illinois, USA.
Aliment Pharmacol Ther. 2022 May;55(9):1151-1159. doi: 10.1111/apt.16805. Epub 2022 Feb 15.
It is unclear whether improvement in patient-reported outcomes (PROs) relative to baseline symptom burden in Crohn's disease (CD) is associated with subsequent endoscopic remission.
To evaluate the relationship between dominant PRO resolution post-induction and achievement of clinical and endoscopic remission.
This post-hoc analysis of clinical trial data from 251 participants evaluated the relationship between the resolution of the dominant PRO (most severely elevated baseline PRO) or clinical response (CDAI ≥100 reduction) after induction therapy with biologics (post-induction) and 1-year clinical remission (CDAI <150) and/or endoscopic remission (SES-CD <3). Multivariate logistic regression models evaluated the relationship between post-induction-dominant PRO resolution and 1-year outcomes adjusted for confounders.
Participants with dominant PRO resolution post-induction had higher odds of combined endoscopic and clinical remission compared to those without resolution (aOR: 1.94 [95% CI: 1.01-3.74], P = 0.047). Combining dominant PRO resolution with post-induction endoscopic response (SES-CD ≥50% reduction) was associated with higher odds of 1-year endoscopic and clinical remission (aOR: 6.89 [95% CI: 1.65-28.72], P = 0.008). Clinical and PRO2 response (≥30% decrease in stool frequency and/or ≥30% decrease in abdominal pain score and both not worse than baseline) at post-induction did not predict these outcomes. No significant differences were observed with 1-year endoscopic remission for post-induction-dominant PRO resolution, clinical or PRO2 response.
Post-induction resolution of dominant PRO, but not clinical or PRO2 response, was strongly associated with 1-year endoscopic and clinical remission. Resolution of dominant baseline PRO after induction therapy may be informative for 1-year outcomes. Further validation is required.
尚不清楚克罗恩病(CD)患者报告结局(PRO)相对于基线症状负担的改善是否与随后的内镜缓解相关。
评估诱导后主要 PRO 缓解与临床和内镜缓解的关系。
对 251 名参与者的临床试验数据进行了此项事后分析,评估了诱导后生物制剂治疗后主要 PRO(基线 PRO 升高最严重者)或临床应答(CDAI 降低≥100)的缓解与 1 年临床缓解(CDAI <150)和/或内镜缓解(SES-CD <3)之间的关系。多变量逻辑回归模型评估了在调整混杂因素后,诱导后主要 PRO 缓解与 1 年结局之间的关系。
与未缓解者相比,诱导后主要 PRO 缓解者有更高的联合内镜和临床缓解的几率(优势比:1.94 [95%可信区间:1.01-3.74],P=0.047)。将诱导后主要 PRO 缓解与内镜缓解反应(SES-CD 降低≥50%)相结合与 1 年内镜和临床缓解的几率较高相关(优势比:6.89 [95%可信区间:1.65-28.72],P=0.008)。诱导后临床和 PRO2 应答(粪便频率减少≥30%和/或腹痛评分减少≥30%,且均不劣于基线)并不能预测这些结局。在诱导后主要 PRO 缓解、临床或 PRO2 应答与 1 年内镜缓解之间,未观察到显著差异。
诱导后主要 PRO 的缓解,而不是临床或 PRO2 应答,与 1 年的内镜和临床缓解强烈相关。诱导后治疗主要基线 PRO 的缓解可能对 1 年结局有提示作用。需要进一步验证。