{"title":"研究简介","authors":"Holly Baker","doi":"10.1016/s2468-1253(24)00403-5","DOIUrl":null,"url":null,"abstract":"<h2>Section snippets</h2><section><section><h2>Mirikizumab for Crohn's disease</h2>Mirikizumab, a monoclonal antibody targeting IL-23p19, shows promise for patients with moderately-to-severely active Crohn's disease, according to the <span><span>VIVID-1 phase 3 trial</span><svg aria-label=\"Opens in new window\" focusable=\"false\" height=\"20\" viewbox=\"0 0 8 8\"><path d=\"M1.12949 2.1072V1H7V6.85795H5.89111V2.90281L0.784057 8L0 7.21635L5.11902 2.1072H1.12949Z\"></path></svg></span>. Marc Ferrante and colleagues randomly assigned patients who had a previous inadequate response, loss of response, or intolerance to one or more therapies to receive either mirikizumab (n=579), ustekinumab (n=287), or placebo (n=199). The coprimary composite endpoints (mirikizumab <em>vs</em> placebo) were the proportion of patients</section></section><section><section><h2>Endoscopic sphincterotomy for post-ERCP pancreatitis</h2>Endoscopic sphincterotomy does not reduce the risk of pancreatitis following endoscopic retrograde cholangiopancreatography (ERCP) in patients undergoing biliary drainage for distal malignant biliary obstruction, according to the <span><span>SPHINX trial</span><svg aria-label=\"Opens in new window\" focusable=\"false\" height=\"20\" viewbox=\"0 0 8 8\"><path d=\"M1.12949 2.1072V1H7V6.85795H5.89111V2.90281L0.784057 8L0 7.21635L5.11902 2.1072H1.12949Z\"></path></svg></span>. Anke M Onnekink and colleagues randomly assigned patients to receive either endoscopic sphincterotomy (n=156) or no sphincterotomy (control group; n=141) before ERCP with fully covered self-expandable metal stent placement. The primary endpoint of</section></section><section><section><h2><span><span>FMT in Crohn's disease</span><svg aria-label=\"Opens in new window\" focusable=\"false\" height=\"20\" viewbox=\"0 0 8 8\"><path d=\"M1.12949 2.1072V1H7V6.85795H5.89111V2.90281L0.784057 8L0 7.21635L5.11902 2.1072H1.12949Z\"></path></svg></span></h2>Faecal microbiota transplantation (FMT) was not efficacious at inducing remission in patients with Crohn's disease, according to a results from a new study. Dina Kao and colleagues randomly assigned patients with mild-to-moderate Crohn's disease to receive either FMT, delivered initially via colonoscopy followed by weekly capsules, or placebo for 7 weeks. The trial was halted early due to futility—at week 8, none (0%) of 15 patients in the FMT group had achieved the primary endpoint of combined</section></section><section><section><h2>Switch maintenance therapy for gastric cancer</h2>Paclitaxel plus ramucirumab as switch maintenance could be a promising treatment strategy for patients with advanced gastric cancer, according to the <span><span>ARMANI phase 3 trial</span><svg aria-label=\"Opens in new window\" focusable=\"false\" height=\"20\" viewbox=\"0 0 8 8\"><path d=\"M1.12949 2.1072V1H7V6.85795H5.89111V2.90281L0.784057 8L0 7.21635L5.11902 2.1072H1.12949Z\"></path></svg></span>. Giovanni Randon and colleagues randomly assigned patients with advanced gastric or gastro-oesophageal junction cancers and disease control after 3 months on first-line chemotherapy (FOLFOX or CAPOX) to switch to paclitaxel plus ramucirumab (switch maintenance group; n=144) or to continue chemotherapy for an additional 12</section></section><section><section><h2><span><span>Carvedilol plus simvastatin for cirrhosis with severe portal hypertension</span><svg aria-label=\"Opens in new window\" focusable=\"false\" height=\"20\" viewbox=\"0 0 8 8\"><path d=\"M1.12949 2.1072V1H7V6.85795H5.89111V2.90281L0.784057 8L0 7.21635L5.11902 2.1072H1.12949Z\"></path></svg></span></h2>The addition of simvastatin to carvedilol might be beneficial for patients with cirrhosis and severe portal hypertension, new research suggests. Edilmar Alvarado-Tapias and colleagues randomly assigned patients with cirrhosis and high-risk varices who showed an inadequate response to traditional non-selective β-blockers to receive either carvedilol plus simvastatin (n=41) or carvedilol plus placebo (n=41). A reduction in hepatic venous pressure gradient (HVPG) of 2·97±2·5 mm Hg was observed in</section></section>","PeriodicalId":56028,"journal":{"name":"Lancet Gastroenterology & Hepatology","volume":"15 1","pages":""},"PeriodicalIF":30.9000,"publicationDate":"2024-12-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Research in Brief\",\"authors\":\"Holly Baker\",\"doi\":\"10.1016/s2468-1253(24)00403-5\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<h2>Section snippets</h2><section><section><h2>Mirikizumab for Crohn's disease</h2>Mirikizumab, a monoclonal antibody targeting IL-23p19, shows promise for patients with moderately-to-severely active Crohn's disease, according to the <span><span>VIVID-1 phase 3 trial</span><svg aria-label=\\\"Opens in new window\\\" focusable=\\\"false\\\" height=\\\"20\\\" viewbox=\\\"0 0 8 8\\\"><path d=\\\"M1.12949 2.1072V1H7V6.85795H5.89111V2.90281L0.784057 8L0 7.21635L5.11902 2.1072H1.12949Z\\\"></path></svg></span>. Marc Ferrante and colleagues randomly assigned patients who had a previous inadequate response, loss of response, or intolerance to one or more therapies to receive either mirikizumab (n=579), ustekinumab (n=287), or placebo (n=199). The coprimary composite endpoints (mirikizumab <em>vs</em> placebo) were the proportion of patients</section></section><section><section><h2>Endoscopic sphincterotomy for post-ERCP pancreatitis</h2>Endoscopic sphincterotomy does not reduce the risk of pancreatitis following endoscopic retrograde cholangiopancreatography (ERCP) in patients undergoing biliary drainage for distal malignant biliary obstruction, according to the <span><span>SPHINX trial</span><svg aria-label=\\\"Opens in new window\\\" focusable=\\\"false\\\" height=\\\"20\\\" viewbox=\\\"0 0 8 8\\\"><path d=\\\"M1.12949 2.1072V1H7V6.85795H5.89111V2.90281L0.784057 8L0 7.21635L5.11902 2.1072H1.12949Z\\\"></path></svg></span>. Anke M Onnekink and colleagues randomly assigned patients to receive either endoscopic sphincterotomy (n=156) or no sphincterotomy (control group; n=141) before ERCP with fully covered self-expandable metal stent placement. The primary endpoint of</section></section><section><section><h2><span><span>FMT in Crohn's disease</span><svg aria-label=\\\"Opens in new window\\\" focusable=\\\"false\\\" height=\\\"20\\\" viewbox=\\\"0 0 8 8\\\"><path d=\\\"M1.12949 2.1072V1H7V6.85795H5.89111V2.90281L0.784057 8L0 7.21635L5.11902 2.1072H1.12949Z\\\"></path></svg></span></h2>Faecal microbiota transplantation (FMT) was not efficacious at inducing remission in patients with Crohn's disease, according to a results from a new study. Dina Kao and colleagues randomly assigned patients with mild-to-moderate Crohn's disease to receive either FMT, delivered initially via colonoscopy followed by weekly capsules, or placebo for 7 weeks. The trial was halted early due to futility—at week 8, none (0%) of 15 patients in the FMT group had achieved the primary endpoint of combined</section></section><section><section><h2>Switch maintenance therapy for gastric cancer</h2>Paclitaxel plus ramucirumab as switch maintenance could be a promising treatment strategy for patients with advanced gastric cancer, according to the <span><span>ARMANI phase 3 trial</span><svg aria-label=\\\"Opens in new window\\\" focusable=\\\"false\\\" height=\\\"20\\\" viewbox=\\\"0 0 8 8\\\"><path d=\\\"M1.12949 2.1072V1H7V6.85795H5.89111V2.90281L0.784057 8L0 7.21635L5.11902 2.1072H1.12949Z\\\"></path></svg></span>. Giovanni Randon and colleagues randomly assigned patients with advanced gastric or gastro-oesophageal junction cancers and disease control after 3 months on first-line chemotherapy (FOLFOX or CAPOX) to switch to paclitaxel plus ramucirumab (switch maintenance group; n=144) or to continue chemotherapy for an additional 12</section></section><section><section><h2><span><span>Carvedilol plus simvastatin for cirrhosis with severe portal hypertension</span><svg aria-label=\\\"Opens in new window\\\" focusable=\\\"false\\\" height=\\\"20\\\" viewbox=\\\"0 0 8 8\\\"><path d=\\\"M1.12949 2.1072V1H7V6.85795H5.89111V2.90281L0.784057 8L0 7.21635L5.11902 2.1072H1.12949Z\\\"></path></svg></span></h2>The addition of simvastatin to carvedilol might be beneficial for patients with cirrhosis and severe portal hypertension, new research suggests. Edilmar Alvarado-Tapias and colleagues randomly assigned patients with cirrhosis and high-risk varices who showed an inadequate response to traditional non-selective β-blockers to receive either carvedilol plus simvastatin (n=41) or carvedilol plus placebo (n=41). 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引用次数: 0
摘要
mirikizumab是一种靶向IL-23p19的单克隆抗体,根据VIVID-1 iii期临床试验显示,mirikizumab有望用于中度至重度活动性克罗恩病患者。Marc Ferrante及其同事随机分配先前对一种或多种治疗反应不足、反应丧失或不耐受的患者接受mirikizumab (n=579)、ustekinumab (n=287)或安慰剂(n=199)。根据SPHINX试验,主要复合终点(mirikizumab与安慰剂)是内镜下括约肌切开术治疗ERCP后胰腺炎的患者比例。内镜下括约肌切开术不能降低因远端恶性胆道梗阻而行胆道引流的患者内镜下逆行胆道造影术(ERCP)后胰腺炎的风险。Anke M Onnekink及其同事随机分配患者接受内窥镜括约肌切开术(n=156)或不接受括约肌切开术(对照组;n=141)在ERCP前置入全覆盖自膨胀金属支架。根据一项新研究的结果,粪便微生物群移植(FMT)在诱导克罗恩病患者缓解方面无效。Dina Kao及其同事随机分配轻度至中度克罗恩病患者接受FMT治疗,最初通过结肠镜检查,随后每周服用胶囊,或安慰剂治疗7周。该试验因无效而提前停止——在第8周时,FMT组的15名患者中没有(0%)达到联合切换维持治疗胃癌的主要终点紫杉醇加ramucirumab,根据ARMANI 3期试验,切换维持治疗可能是晚期胃癌患者的一种有希望的治疗策略。Giovanni Randon及其同事随机分配在一线化疗(FOLFOX或CAPOX) 3个月后疾病控制的晚期胃癌或胃食管结癌患者切换到紫杉醇加ramucirumab(切换维持组;新的研究表明,卡维地洛加辛伐他汀可能对肝硬化和严重门脉高压患者有益。Edilmar Alvarado-Tapias及其同事将对传统非选择性β受体阻滞剂反应不足的肝硬化和高危静脉曲张患者随机分配到卡维地洛加辛伐他汀组(n=41)或卡维地洛加安慰剂组(n=41)。肝静脉压梯度(HVPG)降低2.97±2.5 mm Hg
Mirikizumab, a monoclonal antibody targeting IL-23p19, shows promise for patients with moderately-to-severely active Crohn's disease, according to the VIVID-1 phase 3 trial. Marc Ferrante and colleagues randomly assigned patients who had a previous inadequate response, loss of response, or intolerance to one or more therapies to receive either mirikizumab (n=579), ustekinumab (n=287), or placebo (n=199). The coprimary composite endpoints (mirikizumab vs placebo) were the proportion of patients
Endoscopic sphincterotomy for post-ERCP pancreatitis
Endoscopic sphincterotomy does not reduce the risk of pancreatitis following endoscopic retrograde cholangiopancreatography (ERCP) in patients undergoing biliary drainage for distal malignant biliary obstruction, according to the SPHINX trial. Anke M Onnekink and colleagues randomly assigned patients to receive either endoscopic sphincterotomy (n=156) or no sphincterotomy (control group; n=141) before ERCP with fully covered self-expandable metal stent placement. The primary endpoint of
FMT in Crohn's disease
Faecal microbiota transplantation (FMT) was not efficacious at inducing remission in patients with Crohn's disease, according to a results from a new study. Dina Kao and colleagues randomly assigned patients with mild-to-moderate Crohn's disease to receive either FMT, delivered initially via colonoscopy followed by weekly capsules, or placebo for 7 weeks. The trial was halted early due to futility—at week 8, none (0%) of 15 patients in the FMT group had achieved the primary endpoint of combined
Switch maintenance therapy for gastric cancer
Paclitaxel plus ramucirumab as switch maintenance could be a promising treatment strategy for patients with advanced gastric cancer, according to the ARMANI phase 3 trial. Giovanni Randon and colleagues randomly assigned patients with advanced gastric or gastro-oesophageal junction cancers and disease control after 3 months on first-line chemotherapy (FOLFOX or CAPOX) to switch to paclitaxel plus ramucirumab (switch maintenance group; n=144) or to continue chemotherapy for an additional 12
Carvedilol plus simvastatin for cirrhosis with severe portal hypertension
The addition of simvastatin to carvedilol might be beneficial for patients with cirrhosis and severe portal hypertension, new research suggests. Edilmar Alvarado-Tapias and colleagues randomly assigned patients with cirrhosis and high-risk varices who showed an inadequate response to traditional non-selective β-blockers to receive either carvedilol plus simvastatin (n=41) or carvedilol plus placebo (n=41). A reduction in hepatic venous pressure gradient (HVPG) of 2·97±2·5 mm Hg was observed in
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