Institution
Seoul National University Hospital
Healthcare•Seoul, South Korea•
About: Seoul National University Hospital is a healthcare organization based out in Seoul, South Korea. It is known for research contribution in the topics: Population & Medicine. The organization has 10684 authors who have published 20230 publications receiving 415197 citations. The organization is also known as: Seoul National University Hospital.
Topics: Population, Medicine, Cancer, Breast cancer, Hazard ratio
Papers published on a yearly basis
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TL;DR: Additional extrahepatic collateral vessel chemoembolization should be attempted to increase the therapeutic efficacy of TACE for hepatocellular carcinoma.
Abstract: Extrahepatic collateral arteries commonly supply hepatocellular carcinomas if the tumors are large or peripherally located. Because development of these vessels interferes with effective control of the tumor with transcatheter arterial chemoembolization (TACE), radiologists should become familiar with the imaging findings of extrahepatic collateral vessels to detect them at an early stage. The authors observed 2104 such vessels in 860 patients over 5.5 years. The extrahepatic collateral vessels observed originated from the inferior phrenic artery, omental branch, adrenal artery, intercostal artery, cystic artery, internal mammary artery, renal or renal capsular artery, branch of the superior mesenteric artery, gastric artery, and lumbar artery. The authors suspected extrahepatic collateral vessels when (a) a tumor grew exophytically or invaded adjacent organs, (b) a tumor was in contact with the ligaments and bare area of the liver, (c) a hypertrophied extrahepatic collateral vessel was observed on a computed tomographic (CT) scan, (d) a peripheral defect of iodized oil retention within a tumor was seen during chemoembolization or on a follow-up CT scan, (e) a local recurrence developed at the peripheral portion of the treated tumor during follow-up, or (f) a sustained elevation in serum alpha-fetoprotein level was noted despite adequate embolization of the hepatic artery. When both the hepatic artery and extrahepatic collateral vessels supply a tumor, additional extrahepatic collateral vessel chemoembolization should be attempted to increase the therapeutic efficacy of TACE for hepatocellular carcinoma.
208 citations
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University of Auckland1, Institute of Molecular Pathology and Immunology of the University of Porto2, Memorial Sloan Kettering Cancer Center3, Netherlands Cancer Institute4, Radboud University Nijmegen5, University of Paris6, Royal Melbourne Hospital7, National Institutes of Health8, University of Cambridge9, Stanford University10, Auckland City Hospital11, University of British Columbia12, University of Chicago13, Imperial College London14, University of Texas MD Anderson Cancer Center15, Hamamatsu University School of Medicine16, National Institute for Health Research17, Epigenomics AG18, Seoul National University Hospital19, University of Otago20, University of California, Davis21, University of Zurich22, Christchurch Hospital23, Pontifical Catholic University of Chile24, Instituto Superior Técnico25, University of California, Los Angeles26
TL;DR: In this article, the authors present updated clinical practice guidelines for hereditary diffuse gastric cancer (HDGC) from the International Gastric Cancer Linkage Consortium (IGCLC), which recognise the emerging evidence of variability in Gastric cancer risk between families with HDGC, and increased experience of managing long-term sequelae of total gastrectomy in young patients.
Abstract: Hereditary diffuse gastric cancer (HDGC) is an autosomal dominant cancer syndrome that is characterised by a high prevalence of diffuse gastric cancer and lobular breast cancer. It is largely caused by inactivating germline mutations in the tumour suppressor gene CDH1, although pathogenic variants in CTNNA1 occur in a minority of families with HDGC. In this Policy Review, we present updated clinical practice guidelines for HDGC from the International Gastric Cancer Linkage Consortium (IGCLC), which recognise the emerging evidence of variability in gastric cancer risk between families with HDGC, the growing capability of endoscopic and histological surveillance in HDGC, and increased experience of managing long-term sequelae of total gastrectomy in young patients. To redress the balance between the accessibility, cost, and acceptance of genetic testing and the increased identification of pathogenic variant carriers, the HDGC genetic testing criteria have been relaxed, mainly through less restrictive age limits. Prophylactic total gastrectomy remains the recommended option for gastric cancer risk management in pathogenic CDH1 variant carriers. However, there is increasing confidence from the IGCLC that endoscopic surveillance in expert centres can be safely offered to patients who wish to postpone surgery, or to those whose risk of developing gastric cancer is not well defined.
208 citations
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TL;DR: The presence of extensive drug resistance, the presence of comorbidity, and hypoalbuminemia were independent poor prognostic factors in non-HIV-infected patients with MDR-TB.
Abstract: Recently serious concerns about extensively drug-resistant tuberculosis (XDR-TB) which shows resistance to second-line anti-TB drugs in addition to isoniazid and rifampicin have been raised. The aim of this study was to elucidate the impact of extensive drug resistance on treatment outcomes in non-human immunodeficiency virus (HIV)-infected patients with multidrug-resistant tuberculosis (MDR-TB). Patients who received the diagnosis of and treatment as having MDR-TB at Seoul National University Hospital (Seoul Republic of Korea) between January 1996 and December 2005 were included. The definition of XDR-TB was TB caused by bacilli showing resistance to both isoniazid and rifampicin and also showing resistance to any fluoroquinolone and to at least 1 of the following 3 injectable anti-TB drugs: capreomycin kanamycin and amikacin. To identify the impact of extensive drug resistance on treatment outcomes univariate comparison and multiple logistic regression were performed. A total of 211 non-HIV-infected patients with MDR-TB were included in the final analysis. Among them 43 patients (20.4%) had XDR-TB. Treatment failure was observed in 19 patients (44.2%) with XDR-TB whereas treatment of 46 patients (27.4%) with non-XDR-TB failed (P = .057). The presence of extensive drug resistance (adjusted odds ratio [OR] 4.46; 95% confidence interval [CI] 1.35-14.74) and underlying comorbidity (adjusted OR 2.62; 95% CI 1.00-6.87) were independent risk factors for treatment failure. However a higher level of albumin was inversely associated with treatment failure (adjusted OR 0.87; 95% CI 0.77-0.97). The presence of extensive drug resistance the presence of comorbidity and hypoalbuminemia were independent poor prognostic factors in non-HIV-infected patients with MDR-TB. (authors)
207 citations
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TL;DR: Abdominal obesity, especially visceral obesity, was an important risk factor for reflux oesophagitis and metabolic syndrome was associated with reflux gout.
Abstract: Background: Obesity has been associated with reflux oesophagitis. However, the relationship between metabolic syndrome characterised by visceral obesity and reflux oesophagitis is unclear. Aim: To investigate whether metabolic syndrome or visceral obesity is a risk factor for reflux oesophagitis. Methods: A cross-sectional study of 7078 subjects undergoing upper endoscopy during health check-ups was conducted (3539 patients with reflux oesophagitis vs age- and sex-matched controls). We further analysed according to categories of visceral adipose tissue and subcutaneous adipose tissue area with 750 cases and age-, sex- and waist circumference-matched controls who underwent abdominal CT scan. Results: The prevalence of metabolic syndrome was higher in cases than controls (26.9% vs 18.5%, p 2 ) (136.1 (SD 57.8) vs 124.0 (SD 54.7), p 2 ) (145.9 (SD 56.8) vs 133.5 (SD 50.7), p Conclusions: Metabolic syndrome was associated with reflux oesophagitis. Abdominal obesity, especially visceral obesity, was an important risk factor for reflux oesophagitis.
207 citations
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TL;DR: It is shown that evolutionary inference from integrated genomic analysis in multisector biopsies can inform targeted therapeutic interventions for patients with GBM and that targeting truncal events is more efficacious than targeting private events in reducing the tumor burden.
Abstract: Precision medicine in cancer proposes that genomic characterization of tumors can inform personalized targeted therapies. However, this proposition is complicated by spatial and temporal heterogeneity. Here we study genomic and expression profiles across 127 multisector or longitudinal specimens from 52 individuals with glioblastoma (GBM). Using bulk and single-cell data, we find that samples from the same tumor mass share genomic and expression signatures, whereas geographically separated, multifocal tumors and/or long-term recurrent tumors are seeded from different clones. Chemical screening of patient-derived glioma cells (PDCs) shows that therapeutic response is associated with genetic similarity, and multifocal tumors that are enriched with PIK3CA mutations have a heterogeneous drug-response pattern. We show that targeting truncal events is more efficacious than targeting private events in reducing the tumor burden. In summary, this work demonstrates that evolutionary inference from integrated genomic analysis in multisector biopsies can inform targeted therapeutic interventions for patients with GBM.
206 citations
Authors
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Name | H-index | Papers | Citations |
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Hyun-Chul Kim | 176 | 4076 | 183227 |
Gregory Y.H. Lip | 169 | 3159 | 171742 |
Roberto Romero | 151 | 1516 | 108321 |
Byung-Sik Hong | 146 | 1557 | 105696 |
Taeghwan Hyeon | 139 | 563 | 75814 |
Hyunyong Kim | 114 | 1433 | 65154 |
Yung-Jue Bang | 94 | 664 | 46313 |
Dong Wan Kim | 89 | 833 | 49632 |
Hyo-Soo Kim | 81 | 767 | 30713 |
Byung Ihn Choi | 78 | 609 | 24925 |
Seung-Jung Park | 77 | 503 | 24540 |
Dong Soo Lee | 73 | 729 | 22060 |
J. H. Kim | 73 | 566 | 23052 |
Martin O'Donnell | 73 | 295 | 64065 |
Young Tae Kim | 73 | 876 | 23198 |