P295 早期声像图改善可预测分子靶向药物治疗溃疡性结肠炎的中期疗效

J. Miyoshi, Y. Kimura, H. Morikubo, H. Komatsu, H. Yonezawa, M. Matsuura, T. Hisamatsu
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引用次数: 0

摘要

如今,分子靶向药物(MTMs)已被广泛用于治疗溃疡性结肠炎(UC)。在诱导治疗后的早期预测分子靶向药物的疗效仍然是一项重要的临床挑战。肠道超声(IUS)目前被认为是一种无创、有前景的溃疡性结肠炎监测工具。它可以安全、反复地评估整个结肠中 UC 的疾病活动性。在此,我们假设随着时间的推移,IUS 评估可以及早预测 MTM 的疗效,有助于及早做出是否继续或更换 MTM 的临床决策,并减轻建议在诱导后 6 个月左右进行结肠镜检查 (CS) 的负担。 我们分析了 44 例因活动性 UC 而开始接受 MTM 的患者,他们在基线和 3 个月时接受了 IUS 检查,并在诱导后 6 个月接受了 CS 检查。临床疾病活动度和 6 个月时的内镜活动度分别通过 Lichtiger 指数(LI)和梅奥内镜评分(MES)进行评估。临床缓解的定义是LI≤3。内镜改善(EI)的定义是 MES = 0 或 1。除了评估肠壁厚度(BWT)等超声波检查结果外,还评估了肠壁分层,包括黏膜下指数(SMI)、改良林贝格评分(mLS)、米兰超声标准(MUC)、UC-IUS 指数(UII)、UC 的京林超声标准(KUC-UC;BWT<3.8 毫米,SMI<50%)。 与未达到无类固醇临床缓解(SFCR)的患者相比,达到无类固醇临床缓解(SFCR)的患者在3个月内BWT、%BWT和mLS的改善程度更好(P<0.01)。在 6 个月时达到 SFCR 的患者中也观察到了 MUC 和 UII 的改善(均为 p<0.001)。在 ROC 分析中,6 个月时 SFCR 的曲线下面积与 BWT 的关系为 0.80,与 %BWT 的关系为 0.80,与 mLS 的关系为 0.81,与 MUC 的关系为 0.85,与 UII 的关系为 0.85。在 44 名患者中,有 7 名患者在 3 个月时 MUC≤ 6.2,估计 MES=0/1, 7 名患者中有 6 名在 6 个月时表现为 EI(阳性预测值 [PPV] =87.5%)。同时,4 名患者在 3 个月时符合 KUC-UC 标准,且所有患者在 6 个月时都达到了 SFCR 和 EI(PPV=100%)。 我们的研究表明,在 3 个月内声像图结果改善的患者可以继续进行 MTM 治疗,而在 3 个月内声像图结果显示 EI 的患者可以在 6 个月内推迟 CS。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
P295 Early sonographic improvement predicts the middle-term efficacy of molecular-targeted medications for Ulcerative Colitis
Today molecular-targeted medications (MTMs) are widely used for ulcerative colitis (UC). Predicting the efficacy of MTMs early after induction remains a crucial clinical challenge. Intestinal ultrasound (IUS) is now considered a non-invasive, promising monitoring tool for UC. It can assess the disease activity of UC in the whole colon safely and repeatedly. Here, we hypothesized that over time IUS assessment can predict the MTM efficacy early, contribute to early clinical decision-making on whether to continue or switch MTMs, and reduce the burden of colonoscopy (CS) recommended to be scheduled at around 6 months after the induction. We analyzed 44 patients who started an MTM for active UC, underwent IUS at baseline and 3 months, and took CS at 6 months after the induction. The clinical disease activity and endoscopic activity at 6 months were assessed with Lichtiger index (LI) and Mayo endoscopic subscore (MES), respectively. Clinical remission was defined as a LI ≤ 3. Endoscopic improvement (EI) was defined as a MES = 0 or 1. In addition to the assessment of sonographic findings, such as bowel wall thickness (BWT), bowel wall stratification including submucosa index (SMI), bowel wall flow with modified Limberg score (mLS), Milan Ultrasound Criteria (MUC), UC-IUS index (UII), Kyorin Ultrasound Criterion for UC (KUC-UC; BWT<3.8mm with SMI<50%) were evaluated. Patients who achieved steroid-free clinical remission (SFCR) showed better improvement in BWT, %BWT, and mLS in 3 months compared to those who did not achieve SFCR (p<0.01 for each). The improvement in MUC and UII was also observed in patients who achieved SFCR at 6 months (p<0.001 for both). In ROC analyses, the area under the curve for SFCR at 6 months was 0.80 with BWT, 0.80 with %BWT, 0.81 with mLS, 0.85 with MUC, and 0.85 with UII. Among the 44 patients, 7 patients achieved MUC≤ 6.2, estimating MES=0/1, at 3 months, and 6 out of 7 patients demonstrated EI at 6 months (positive predictive value [PPV]=87.5%). Meanwhile, 4 patients satisfied KUC-UC at 3 months and all of them achieved SFCR and EI at 6 months (PPV=100%). Our study suggests that patients who achieved sonographic improvement in 3 months can continue an ongoing MTM therapy and that patients who demonstrated sonographic findings estimating EI at 3 months can postpone CS at 6 months.
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