Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Department of Gastroenterology and Hepatology, Kyung Hee University School of Medicine, Seoul, Korea.
Gastrointest Endosc. 2022 Mar;95(3):500-511.e2. doi: 10.1016/j.gie.2021.09.041. Epub 2021 Oct 12.
The 1-L polyethylene glycol (PEG)-based bowel preparation agent NER1006 (Plenvu; Norgine, Harefield, UK) has shown high cleansing efficacy and tolerability in clinical trials in Europe and North America. However, no clinical trials have yet been reported in Asia. Therefore, the aim of this study was to evaluate the efficacy and safety of 1L PEG-based bowel preparation with Plenvu compared with 2L PEG plus ascorbate bowel preparation in a Korean population.
In this multicenter, endoscopist-blinded, randomized study, patients at 9 hospitals in South Korea undergoing colonoscopy received either Plenvu or 2L PEG + ascorbate (2L PEG) with a split dose. The primary endpoint was overall bowel cleansing success (Boston Bowel Preparation Scale [BBPS] score ≥2 for all segments of the colon). Secondary endpoints were high-quality bowel cleansing success (overall, BBPS score = 9; segmental colon, BPPS score = 3), polyp detection rate (PDR), and adenoma detection rate (ADR).
Of 360 included patients, cleansing efficacy was analyzed in 346 (Plenvu, 174; 2L PEG, 172). The Plenvu group showed noninferior bowel cleansing success rates compared with 2L PEG (93.10% vs 91.86%; difference, 1.24%; 1-sided 97.5% lower confidence limit, -4.31%; P < .0001; P = .661). The Plenvu group had higher high-quality bowel cleansing success rates for overall and right-sided colon segments than the 2L PEG group (49.43% vs 37.79% [P = .029] and 60.92% vs 48.84% [P = .024], respectively). The PDR was greater with Plenvu than with 2L PEG (48.85% vs 37.79%, P = .038). However, ADR did not differ between the 2 groups (24.71% vs 20.35%, P = .331). Although treatment-emergent adverse events (TEAEs) were slightly higher in the Plenvu group than in the 2L PEG group (65.71% vs 52.91%, P = .015), most TEAEs were mild (85.55%) and most patients recovered without any management (99.23%).
Plenvu showed noninferior overall bowel cleansing success rates comparable with 2L PEG but greater high-quality bowel cleansing in overall and right-sided colon, which might help improve the PDR in the Asian population. (Clinical trial registration number: KCT0005894.).
1L 聚乙二醇(PEG)为基础的肠道准备剂 NER1006(Plenvu;Norgine, Harefield,英国)在欧洲和北美的临床试验中显示出了较高的清洁效果和耐受性。然而,亚洲尚未有临床试验报告。因此,本研究旨在评估 Plenvu 与 2L PEG+抗坏血酸肠道准备在韩国人群中的疗效和安全性。
这是一项多中心、内镜医师盲法、随机研究,韩国 9 家医院的接受结肠镜检查的患者接受 Plenvu 或 2L PEG+抗坏血酸(2L PEG)分剂量治疗。主要终点是整体肠道清洁成功率(波士顿肠道准备量表[BBPS]评分所有结肠段均≥2)。次要终点是高质量肠道清洁成功率(总体 BBPS 评分=9;结肠节段 BPPS 评分=3)、息肉检出率(PDR)和腺瘤检出率(ADR)。
在纳入的 360 例患者中,346 例(Plenvu 组 174 例,2L PEG 组 172 例)进行了清洁效果分析。Plenvu 组的肠道清洁成功率与 2L PEG 组相当(93.10% vs 91.86%;差异 1.24%;单侧 97.5%置信下限-4.31%;P<0.0001;P=0.661)。Plenvu 组的总体和右侧结肠段的高质量肠道清洁成功率高于 2L PEG 组(49.43% vs 37.79%[P=0.029]和 60.92% vs 48.84%[P=0.024])。Plenvu 组的 PDR 高于 2L PEG 组(48.85% vs 37.79%,P=0.038)。然而,两组的 ADR 无差异(24.71% vs 20.35%,P=0.331)。虽然 Plenvu 组的治疗中出现的不良事件(TEAEs)略高于 2L PEG 组(65.71% vs 52.91%,P=0.015),但大多数 TEAEs 为轻度(85.55%),大多数患者无需任何治疗即可恢复(99.23%)。
Plenvu 显示出非劣效性的整体肠道清洁成功率,与 2L PEG 相当,但在总体和右侧结肠段的高质量肠道清洁方面效果更好,这可能有助于提高亚洲人群的 PDR。(临床试验注册号:KCT0005894)。