研究简介

IF 30.9 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Holly Baker
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In the simvastatin plus rifaximin group, 21 (18%) patients experienced acute-on-chronic liver failure compared with 17 (14%) in</section></section><section><section><h2>Nivolumab plus ipilimumab for metastatic colorectal cancer</h2>Nivolumab plus ipilimumab shows potential as a new standard of care for microsatellite instability-high or mismatch repair-deficient metastatic colorectal cancer, according to the <span><span>CheckMate 8HW 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>.Thierry André and colleagues randomly assigned immunotherapy-naive patients to receive either nivolumab plus ipilimumab (n=354) or nivolumab alone (n=353). At median follow-up of 47·0 months (IQR 38·4–53·2), median progression-free survival was not reached in the nivolumab plus ipilimumab</section></section><section><section><h2>Tiragolumab for advanced liver cancer</h2>The addition of tiragolumab, an anti-TIGIT monoclonal antibody, to the established atezolizumab–bevacizumab regimen shows promise in patients with locally advanced or metastatic unresectable hepatocellular carcinoma, according to the <span><span>MORPHEUS-Liver phase 1b–2 study</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>.Richard S Finn and colleagues randomly assigned previously untreated patients to receive either tiragolumab plus atezolizumab plus bevacizumab (n=41) or atezolizumab plus bevacizumab (n=18) every 3 weeks. At clinical cutoff, the</section></section><section><section><h2>Carbon footprint of gastrointestinal endoscopy</h2>Gastrointestinal endoscopy procedures contribute significantly to healthcare-related carbon emissions and waste generation, according to <span><span>new research</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> from India.Hardik Rughwani and colleagues analysed data from 3873 procedures performed on 3244 patients over a 13-day period, assessing greenhouse gas emissions. The total carbon footprint was nearly 150 000 kg CO<sub>2</sub>e, averaging 38·45 kg CO<sub>2</sub>e per procedure, which dropped to 6·50 kg CO<sub>2</sub>e when excluding patient travel. 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引用次数: 0

摘要

辛伐他汀加利福昔明治疗失代偿性肝硬化根据LIVERHOPE 3期试验,在标准治疗中添加辛伐他汀加利福昔明并不能改善失代偿性肝硬化患者的预后。Elisa Pose和同事随机分配失代偿性肝硬化患者,在标准治疗的基础上接受辛伐他汀+利福昔明(n=117)或安慰剂(n=120) 12个月。在辛伐他汀+利福昔明组中,21例(18%)患者经历了急性慢性肝衰竭,而inNivolumab + ipilimumab治疗转移性结直肠癌的患者为17例(14%)。根据CheckMate 8HW 3期试验,nivolumab + ipilimumab显示出作为微卫星不稳定性高或错配修复缺陷转移性结直肠癌的新护理标准的潜力。Thierry andr及其同事随机分配免疫治疗初治患者接受纳武单抗联合伊匹单抗(n=354)或单独纳武单抗(n=353)。在中位随访47.0个月(IQR 38.4 - 52.3)时,尼武单抗联合伊匹单抗替拉单抗治疗晚期肝癌的中位无进展生存期未达到。根据MORPHEUS-Liver 1b-2期研究,在已建立的阿特唑单抗-贝伐单抗方案中加入抗tigit单克隆抗体替拉单抗,对局部晚期或转移性不可切除的肝细胞癌患者显示出希望。Richard S Finn及其同事随机分配先前未接受治疗的患者,每3周接受一次替拉单抗+阿特唑单抗+贝伐单抗(n=41)或阿特唑单抗+贝伐单抗(n=18)。根据印度的一项新研究,胃肠道内窥镜检查程序对医疗保健相关的碳排放和废物产生有重大贡献。Hardik Rughwani和他的同事分析了3244名患者在13天内进行的3873次手术的数据,评估了温室气体排放。总碳足迹接近15万公斤二氧化碳当量,平均每次手术38·45公斤二氧化碳当量,在排除患者旅行后下降到6·50公斤二氧化碳当量。在病人旅行之后
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Research in Brief

Section snippets

Simvastatin plus rifaximin for decompensated cirrhosis

The addition of simvastatin plus rifaximin to standard therapy does not improve outcomes in patients with decompensated liver cirrhosis, according to the LIVERHOPE phase 3 trial.Elisa Pose and colleagues randomly assigned patients with decompensated cirrhosis to receive simvastatin plus rifaximin (n=117) or placebo (n=120) for 12 months in addition to standard therapy. In the simvastatin plus rifaximin group, 21 (18%) patients experienced acute-on-chronic liver failure compared with 17 (14%) in

Nivolumab plus ipilimumab for metastatic colorectal cancer

Nivolumab plus ipilimumab shows potential as a new standard of care for microsatellite instability-high or mismatch repair-deficient metastatic colorectal cancer, according to the CheckMate 8HW phase 3 trial.Thierry André and colleagues randomly assigned immunotherapy-naive patients to receive either nivolumab plus ipilimumab (n=354) or nivolumab alone (n=353). At median follow-up of 47·0 months (IQR 38·4–53·2), median progression-free survival was not reached in the nivolumab plus ipilimumab

Tiragolumab for advanced liver cancer

The addition of tiragolumab, an anti-TIGIT monoclonal antibody, to the established atezolizumab–bevacizumab regimen shows promise in patients with locally advanced or metastatic unresectable hepatocellular carcinoma, according to the MORPHEUS-Liver phase 1b–2 study.Richard S Finn and colleagues randomly assigned previously untreated patients to receive either tiragolumab plus atezolizumab plus bevacizumab (n=41) or atezolizumab plus bevacizumab (n=18) every 3 weeks. At clinical cutoff, the

Carbon footprint of gastrointestinal endoscopy

Gastrointestinal endoscopy procedures contribute significantly to healthcare-related carbon emissions and waste generation, according to new research from India.Hardik Rughwani and colleagues analysed data from 3873 procedures performed on 3244 patients over a 13-day period, assessing greenhouse gas emissions. The total carbon footprint was nearly 150 000 kg CO2e, averaging 38·45 kg CO2e per procedure, which dropped to 6·50 kg CO2e when excluding patient travel. After patient travel, the
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来源期刊
CiteScore
50.30
自引率
1.10%
发文量
0
期刊介绍: The Lancet Gastroenterology & Hepatology is an authoritative forum for key opinion leaders across medicine, government, and health systems to influence clinical practice, explore global policy, and inform constructive, positive change worldwide. The Lancet Gastroenterology & Hepatology publishes papers that reflect the rich variety of ongoing clinical research in these fields, especially in the areas of inflammatory bowel diseases, NAFLD and NASH, functional gastrointestinal disorders, digestive cancers, and viral hepatitis.
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