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Appropriateness of systemic treatments in unresectable metastatic well-differentiated pancreatic neuroendocrine tumors 被引量:2
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作者 Jonathan R Strosberg George A Fisher +11 位作者 Al B Benson Lowell B Anthony Bulent Arslan John F Gibbs Edward Greeno Renuka V Iyer Michelle K Kim William J Maples Philip A Philip Edward M Wolin Dasha Cherepanov Michael S Broder 《World Journal of Gastroenterology》 SCIE CAS 2015年第8期2450-2459,共10页
AIM:To evaluate systemic treatment choices in unresectable metastatic well-differentiated pancreatic neuroendocrine tumors(PNETs)and provide consensus treatment recommendations.METHODS:Systemic treatment options for p... AIM:To evaluate systemic treatment choices in unresectable metastatic well-differentiated pancreatic neuroendocrine tumors(PNETs)and provide consensus treatment recommendations.METHODS:Systemic treatment options for pancreatic neuroendocrine tumors have expanded in recent years to include somatostatin analogs,angiogenesis inhibitors,inhibitors of mammalian target of rapamycinand cytotoxic agents.At this time,there is little data to guide treatment selection and sequence.We therefore assembled a panel of expert physicians to evaluate systemic treatment choices and provide consensus treatment recommendations.Treatment appropriateness ratings were collected using the RAND/UCLA modified Delphi process.After studying the literature,a multidisciplinary panel of 10 physicians assessed the appropriateness of various medical treatment scenarios on a 1-9 scale.Ratings were done both before and after an extended discussion of the evidence.Quantitative measurements of agreement were made and consensus statements developed from the second round ratings.RESULTS:Specialties represented were medical and surgical oncology,interventional radiology,and gastroenterology.Panelists had practiced for a mean of15.5 years(range:6-33).Among 202 rated scenarios,disagreement decreased from 13.2%(26 scenarios)before the face-to-face discussion of evidence to 1%(2)after.In the final ratings,46.5%(94 scenarios)were rated inappropriate,21.8%(44)were uncertain,and30.7%(62)were appropriate.Consensus statements from the scenarios included:(1)it is appropriate to use somatostatin analogs as first line therapy in patients with hormonally functional tumors and may be appropriate in patients who are asymptomatic;(2)it is appropriate to use everolimus,sunitinib,or cytotoxic chemotherapy therapy as first line therapy in patients with symptomatic or progressive tumors;and(3)beyond first line,these same agents can be used.In patients with uncontrolled secretory symptoms,octreotide LAR doses can be titrated up to 60 mg every4 wk or up to 40 mg every 3 or 4 wk.CONCLUSION:Using the Delphi process allowed physician experts to systematically obtain a consensus on the appropriateness of a variety of medical therapies in patients with PNETs. 展开更多
关键词 UNRESECTABLE NEUROENDOCRINE CARCINOMAS Neuroendocr
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Long-term prognostic role of adiponectin in stable coronary artery disease: A meta-analysis of prospective studies
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作者 Sahas Reddy Jitta Priyanka Vatsavayi +11 位作者 Chenna Reddy Tera Shobana Krishnamurthy Saisree Reddy Adla Jala Diksha Sanjana Pasnoor Utheja Dasari Aisha Farooq Supriya Maramreddy Kavya Jammula Medha Reddy Kesani Sridevi Tripuraneni Nihar Jena Rupak Desai 《World Journal of Cardiology》 2025年第6期153-162,共10页
BACKGROUND The persistent burden of cardiovascular(CV)disease in the United States requires innovative and cost-effective prognostic markers that can be relied upon.AIM To provide insights into how adiponectin can pre... BACKGROUND The persistent burden of cardiovascular(CV)disease in the United States requires innovative and cost-effective prognostic markers that can be relied upon.AIM To provide insights into how adiponectin can predict all-cause mortality and major adverse CV events(MACE)in patients with coronary artery disease(CAD)and to determine the prognostic value of adiponectin in predicting all-cause mortality and MACE in patients with stable CAD.METHODS We conducted a systematic search on PubMed,Scopus,and Google Scholar to find relevant studies published through June 2023 evaluating the long-term prognostic role of adiponectin in patients with stable CAD.Using a random effects model with 95%CI,we estimated the odds ratio(OR)while assessing heterogeneity through I^(2)statistics.To ensure robustness,we performed a sensitivity analysis using the leave-one-out approach.RESULTS After screening,we included five prospective studies involving 3225 patients who were followed up for a median duration of 3.8 years.Within the study population,prevalent risk factors included hypertension,diabetes,hyperlipidemia,and smoking.The commonly prescribed medications were angiotensin-converting enzyme inhibitors,beta blockers,and statins.The combined adjusted OR for all-cause mortality was found to be 2.51(95%CI:1.36–4.62),showing heterogeneity(I^(2)=65.51%,P=0.03).On the other hand,the combined adjusted OR for MACE was determined to be 1.04(95%CI:1.02–1.06)with no significant heterogeneity observed(I^(2)=0%,P=0.68).Through a sensitivity analysis,it was discovered that none of the studies significantly impacted the overall results of the meta-analysis,thus indicating their robustness.CONCLUSION Higher levels of adiponectin were found to be associated with an increased risk of long-term mortality and MACE in patients with CAD,which highlights its potential as a cost-effective marker for risk assessment and guiding treatment strategies.Further research on the role of adiponectin could greatly influence decision-making and resource allocation in CV care. 展开更多
关键词 ADIPONECTIN Stable coronary artery disease Coronary artery disease Major adverse cardiac and cerebrovascular events Mortality LONG-TERM Systematic review META-ANALYSIS
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美国医学遗传学会对基因芯片拷贝数变异结果解读指南 被引量:10
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作者 Hutton M.Kearney Erik C.Thorl +4 位作者 Kerry K.Brown Fabiola Quintero-Rivera Sarah T.South 吴畏 刘嘉茵 《国际生殖健康/计划生育杂志》 CAS 2014年第3期217-222,共6页
全基因组芯片已被推荐作为分析智力障碍、孤独症、多发性出生缺陷病因的首要筛查手段,通过芯片检查发现了人类基因组中大量的拷贝数变异(copy number variation,CNV),这些变异中既有正常个体的多态性,也有新发的致病性变异。为帮助临床... 全基因组芯片已被推荐作为分析智力障碍、孤独症、多发性出生缺陷病因的首要筛查手段,通过芯片检查发现了人类基因组中大量的拷贝数变异(copy number variation,CNV),这些变异中既有正常个体的多态性,也有新发的致病性变异。为帮助临床实验室对芯片结果的解读保持一致性,美国医学遗传学会制定了此有关CNV的解读指南。该指南主要应用于产后的分子遗传诊断中。 展开更多
关键词 CNV 拷贝数变异 芯片 比较基因组杂交芯片 全基因组芯片
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