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| 1 | 帕博利珠单抗治疗伴脑转移NSCLC患者的一项非随机、开放Ⅱ期试验的长期随访结果和生物标志物分析显示文摘背景与目的我们开展了一项帕博利珠单抗用于伴未治疗脑转移的非小细胞肺癌(non-small cell lung cancer,NSCLC)或黑色素瘤患者的疗效和安全性的II期试验,旨在评估程序性死亡受体1(programmed cell death 1,PD-1)抑制剂在中枢神经系统(central nervous system,CNS)中的疗效。中期结果已发表,现报道对NSCLC队列的更新分析结果。方法这是一项开放性、单中心、II期试验。纳入标准:年龄≥18岁,诊断为晚期NSCLC并伴有≥1个5 mm-20 mm脑转移病灶,既往从未治疗或之前放疗后进展,无神经系统症状,不需要激素治疗且美国东部肿瘤协作组(Eastern Cooperative Oncology Group,ECOG)<2分。患者每2周接受一次帕博利珠单抗(10 mg/kg)治疗。队列1为程序性死亡配体1(programmed cell death ligand 1,PD-L1)≥1%的患者,队列2为PD-L1<1%或未评估的患者。主要终点是脑转移患者缓解比例。所有经治患者均纳入疗效与安全性终点的分析。该研究已结束入组,并于Clinicaltrials.gov登记注册,注册号为NCT02085070。结果2014年3月31日-2018年5月21日,共42例患者接受治疗。中位随访时间为8.3个月(IQR:4.5个月-26.2个月)。队列1的37例患者中11例有脑转移缓解[29.7%(95%CI:15.9%-47.0%)]。队列2未观察到缓解。治疗相关的3级-4级不良事件(adverse events,AEs)包括2例肺炎、1例全身症状、1例结肠炎、1例肾上腺皮质功能不全、1例高血糖症和1例低钾血症。6例(14%)患者发生了治疗相关的严重不良事件,包括肺炎、急性肾损伤、低钾血症和肾上腺皮质功能不全。没有观察到治疗相关死亡病例。结论帕博利珠单抗治疗PD-L1≥1%的NSCLC伴脑转移患者有效,且对所有纳入的未经治疗的脑转移患者安全。需要进一步探索免疫治疗用于NSCLC合并CNS转移。 | Sarah B GOLDBERG Kurt A SCHALPER Scott N GETTINGER Amit MAHAJAN Roy S HERBST Anne C CHANG Rogerio LILENBAUM Frederick H WILSON Sacit Bulent OMAY James B YU Lucia JILAVEANU Thuy TRAN Kira PAVLIK Elin ROWEN Heather GERRSH Annette KOMLO Richa GUPTA Hailey WYATT Matthew RIBEIRO Yuval KLUGER Geyu ZHOU Wei WEI Veronica L CHANG Harriet M KLUGER 董晓荣(翻译/校对) | 2021 | 中国肺癌杂志2021，24，9： | 34 |
| 2 | No association between cyclooxygenase-2 and uridine diphosphate glucuronosyltransferase 1A6 genetic polymorphisms and colon cancer risk显示文摘AIM:To investigate the association of variations in the cyclooxygenase-2(COX2) and uridine diphosphate glucuronosyltransferase 1A6(UGT1A6) genes and non-steroidal anti-inflammatory drugs(NSAIDs) use with risk of colon cancer.METHODS:NSAIDs,which are known to reduce the risk of colon cancer,act directly on COX2 and reduce its activity.Epidemiological studies have associated variations in the COX2 gene with colon cancer risk,but others were unable to replicate this finding.Similarly,enzymes in the UGT1A6 gene have been demonstrated to modify the therapeutic effect of NSAIDs on colon adenomas.Polymorphisms in the UGT1A6 gene have been statistically shown to interact with NSAID intake to influence risk of developing colon adenomas,but not colon cancer.Here we examined the association of tagging single nucleotide polymorphisms(SNPs) in the COX2 and UGT1A6 genes,and their interaction with NSAID consumption,on risk of colon cancer in a population of 422 colon cancer cases and 481 population controls.RESULTS:No SNP in either gene was individually statistically significantly associated with colon cancer,nor did they statistically significantly change the protective effect of NSAID consumption in our sample.Like others,we were unable to replicate the association of variants in the COX2 gene with colon cancer risk(P > 0.05),and we did not observe that these variants modify the protective effect of NSAIDs(P > 0.05).We were able to confirm the lack of association of variants in UGT1A6 with colon cancer risk,although further studies will have to be conducted to confirm the association of these variants with colon adenomas.CONCLUSION:Our study does not support a role of COX2 and UGT1A6 genetic variations in the development of colon cancer. | Cheryl L Thompson Sarah J Plummer Alona Merkulova Iona Cheng Thomas C Tucker Graham Casey Li Li | 2009 | World Journal of Gastroenterology2009，15，18： | 11 |
| 3 | No association between phosphatase and tensin homolog genetic polymorphisms and colon cancer显示文摘AIM: To investigate the association between single nucleotide polymorphisms (SNPs) in the phosphatase and tensin homolog (PTEN) tumor suppressor gene and risk of colon cancer. METHODS: We utilized a population-based casecontrol study of incident colon cancer individuals (n= 421) and controls (n = 483) aged ≥ 30 years to conduct a comprehensive tagSNP association analysis of the PTEN gene. RESULTS: None of the PTEN SNPs were statistically significantly associated with colon cancer when controlled for age, gender, and race, or when additionally adjusted for other known risk factors (P > 0.05). Haplotype analyses similarly showed no association between the PTEN gene and colon cancer. CONCLUSION: Our study does not support PTEN as a colon cancer susceptibility gene. | Lynette S Phillips Cheryl L Thompson Alona Merkulova Sarah J Plummer Thomas C Tucker Graham Case Li Li | 2009 | World Journal of Gastroenterology2009，15，30： | 2 |
| 4 | Obesity and cardiometabolic disease risk factors among US adolescents with disabilities显示文摘AIM: To generate prevalence estimates of weight status and cardiometabolic disease risk factors among adolescents with and without disabilities.METHODS: Analysis of the 1999-2010 National Health and Nutrition Examination Survey data was conducted among 12-18 years old with(n = 256) and without disabilities(n = 5020). Mean values of waist circumference, fasting glucose, high-density-lipoprotein cholesterol, triglycerides, systolic and diastolic blood pressure and metabolic syndrome(Met S, ≥ 3 risk factors present) were examined by the following standardized body mass index(BMI) categories for those with and without disabilities; overweight(BMI ≥ 85th- < 95 th percentile for age and sex), obesity(BMI ≥ 95 th percentile) and severe obesity(BMI ≥35 kg/m2). Linear regression models were fit with each cardiometabolic disease risk factor independently as continuous outcomes to show relationships with disability status. RESULTS: Adolescents with disabilities were significantlymore likely to be overweight(49.3%), obese(27.6%) and severely obese(12%) vs their peers without disabilities(33.1%, 17.5% and 3.6%, respectively, P ≤ 0.01 for all). A higher proportion of overweight, obese and severely obese children with disabilities had abnormal SBP, fasting lipids and glucose as well as Met S(18.9% of overweight, 32.3% of obese, 55% of severely obese) vs their peers without disabilities(9.7%, 16.8%, 36.3%, respectively). US adolescents with disabilities are over three times as likely to have Met S(OR = 3.45, 95%CI: 1.08-10.99, P = 0.03) vs their peers with no disabilities.CONCLUSION: Results show that adolescents with disabilities are disproportionately affected by obesity and poor cardiometabolic health vs their peers with no disabilities. Health care professionals should monitor the cardiometabolic health of adolescents with disabilities. | Sarah E Messiah Denise C Vidot Gabriel Somarriba Kanathy Haney Semra Aytur Ruby A Natale Jeffrey P Brosco Kristopher L Arheart | 2015 | World Journal of Diabetes2015，6，1： | 2 |
| 5 | Disease complex in coffee involving Meliodogyne arabicida and Fusarium oxysporus 显示文摘 | BERTRAND B NUNEZ C SARAH J L | 2000 | Plant Pathology2000，49，： | 1 |
| 6 | Effects of B-vitamins on plasma homocysteine concentrations and on risk of cardiovascular disease and dementia 显示文摘 | Robert C Sarah L Paul S | 2007 | Curt Opin Clin Nutr Metab Care2007，10，1： | 1 |
| 7 | Panniculitis in childhood显示文摘 | Ingrid C Polcari Sarah L Stein | 2010 | Dermatologic Therapy2010，23，： | 1 |
| 8 | Analysis of Glyphosate, Glufosinate and Aminomethylphosphonic Acid by Capillary Electrophoresis with Indirect Fluorescence Detection显示文摘 | SARAH Y C CHIA-HUNG L | 2002 | Journal of Chromatoqraphy A2002，959，12： | 1 |
| 9 | Galectin-3 regulates myofibroblast activation and hepatic fibrosis显示文摘 | Neil C Alison C Sarah L | 2006 | Proc Natl Acad Sci U S A2006，103，13： | 1 |
| 10 | Abrogation of growth hormone secretion rescues fatty liver in mice with hepatocyte-specific deletion of JAK2显示文摘 | Sos Brandon C Harris Charles Nordstrom Sarah M Tran Jennifer L Balázs Mercedesz Caplazi Patrick Febbraio Maria Applegate Milana A B Wagner Kay-Uwe Weiss Ethan J | 2011 | Journal of Clinical Investigation2011，，4： | 1 |
| 11 | A novel assay for detect- ing canine parvovirus using a quartz crystal microbalance biosen- sor 显示文摘 | Yong K K Seong I L Sarah C | 2015 | J Virol Methods2015，219，： | 1 |
| 12 | Prevalence of maternal smoking and environmental tobacco smoke exposure during pregnancy and impact on birth weight : retrospective study using Millennium Cohort 显示文摘 | Corinne W Sarah L Tim C | 2007 | BMC Public Health2007，7，： | 1 |
| 13 | DHA Exacerbates Experimentally Induced Colitis in SMAD3-/-Mice显示文摘 | HILLARY L W SARAH J M JONATHAN C | 2010 | FASEB Journal2010，24，： | 1 |
| 14 | Effectiveness of inter- ventions targeting physical activity, nutrition and healthy weight for u- niversity and college students:A systematic review and meta-analysis 显示文摘 | RONALD C SARAH A REBECCA L | 2015 | Int J Bebav Nut Phy Act2015，12，1： | 1 |
| 15 | Goodness-of-fit in family context:Infant temperament,marital quality,and early coparenting behavior显示文摘 | Sarah J Sarah C Geoffrey L | 2007 | Infant Behavior and Development2007，30，1： | 1 |
| 16 | Jackson Divergent effects of matrix metalloproteinases 3, 7,9, and 12 on atherosclerotic plaque stability in mouse brachiocephalic arteries显示文摘 | JASON L J SARAH J G ANDREW C | 2005 | PNAS2005，102，15： | 1 |
| 17 | From nanoparticles to hierarchical structures :Controlling the morphology of zeolite beta显示文摘 | Anton P Giorvanni M Sarah C L | 2011 | Microporous and Mesoporous Materials2011，143，： | 1 |
| 18 | Disease complex in coffee involving Meliodogyne arabicida and Fusarium oxysporus显示文摘 | Bertrand B Nunez C Sarah J L | 2000 | Plant Pathology2000，49，： | 1 |
| 19 | Goodness-of-fit in fam- ily context: Infant temperament, marital quality, and early coparenting behavior 显示文摘 | Sarah J Sarah C Geoffrey L | 2007 | Infant Behavior and Develop ment2007，30，1： | 1 |
| 20 | Pharmacology of insect GABA receptors显示文摘 | DAVID B S SARAH C R L JAMES F H W | 1991 | Neurochemical Research1991，16，3： | 1 |
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