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Showing papers by "Thomas W. Rice published in 2012"


Journal ArticleDOI
Cathy Bennett1, Nimish Vakil2, Jacques J. Bergman3, Rebecca Harrison4, Robert D. Odze5, Michael Vieth, Scott Sanders6, Oliver Pech, Gaius Longcroft-Wheaton7, Yvonne Romero8, John M. Inadomi9, Jan Tack10, Douglas A. Corley11, Hendrik Manner, Susi Green7, David Al Dulaimi, Haythem Ali12, Bill Allum13, Mark R Anderson, Howard Curtis14, Gary W. Falk15, M. Brian Fennerty16, Grant Fullarton17, Kausilia K. Krishnadath3, Stephen J. Meltzer18, David Armstrong19, Robert A. Ganz, Gianpaolo Cengia20, James J. Going17, John R. Goldblum21, Charles Gordon22, Heike I. Grabsch23, Chris Haigh, Michio Hongo24, David Johnston25, Ricky Forbes-Young26, Elaine Kay27, Philip Kaye28, Toni Lerut10, Laurence Lovat29, Lars Lundell30, Philip Mairs31, Tadakuza Shimoda32, Stuart J. Spechler33, Stephen J. Sontag34, Peter Malfertheiner35, Iain A. Murray, Manoj Nanji14, David N. Poller7, Krish Ragunath28, Jaroslaw Regula36, Renzo Cestari20, Neil A. Shepherd37, Rajvinder Singh38, Hubert J. Stein, Nicholas J. Talley39, Jean Paul Galmiche40, Tony C.K. Tham41, Peter Watson1, Lisa Yerian21, Massimo Rugge42, Thomas W. Rice21, John Hart43, Stuart Gittens, David Hewin37, Juergen Hochberger, Peter J. Kahrilas44, Sean L. Preston45, Richard E. Sampliner46, Prateek Sharma47, Robert C. Stuart, Kenneth K. Wang8, Irving Waxman43, Chris Abley4, Duncan Loft, Ian D. Penman26, Nicholas J. Shaheen48, Amitabh Chak49, Gareth Davies50, L. J. Dunn51, Yngve Falck-Ytter, John deCaestecker4, Pradeep Bhandari7, Christian Ell, S. Michael Griffin51, Stephen Attwood52, Hugh Barr37, John J.B. Allen53, Mark K. Ferguson43, Paul Moayyedi19, Janusz Jankowski14, Janusz Jankowski4, Janusz Jankowski54 
Queen's University Belfast1, University of Wisconsin-Madison2, University of Amsterdam3, University Hospitals of Leicester NHS Trust4, Harvard University5, University of Warwick6, Queen Alexandra Hospital7, Mayo Clinic8, University of Washington9, Katholieke Universiteit Leuven10, Kaiser Permanente11, Maidstone and Tunbridge Wells NHS Trust12, The Royal Marsden NHS Foundation Trust13, Queen Mary University of London14, University of Pennsylvania15, Oregon Health & Science University16, Glasgow Royal Infirmary17, Johns Hopkins University18, McMaster University19, University of Brescia20, Cleveland Clinic21, Christchurch Hospital22, University of Leeds23, Tohoku University24, Ninewells Hospital25, University of Edinburgh26, Trinity College, Dublin27, Nottingham University Hospitals NHS Trust28, University College London29, Karolinska Institutet30, Valley Hospital31, National Cancer Research Institute32, University of Dallas33, Veterans Health Administration34, Otto-von-Guericke University Magdeburg35, Curie Institute36, Gloucestershire Hospitals NHS Foundation Trust37, University of Adelaide38, University of Newcastle39, University of Nantes40, Ulster Hospital41, University of Padua42, University of Chicago43, Northwestern University44, Barts Health NHS Trust45, University of Arizona46, University of Kansas47, University of North Carolina at Chapel Hill48, Case Western Reserve University49, Harrogate and District NHS Foundation Trust50, Royal Victoria Infirmary51, Durham University52, University of Minnesota53, University of Oxford54
TL;DR: An international, multidisciplinary, systematic, evidence-based review of different management strategies for patients with Barrett's esophagus and dysplasia or early-stage EA and developed a data-sifting platform and used the Delphi process to create evidence- based consensus statements.

359 citations


Journal ArticleDOI
TL;DR: Gefitinib was well tolerated but of limited efficacy in patients with recurrent or metastatic esophageal or GEJ cancer, and further study of this or similar agents will require better patient selection.
Abstract: Background Conventional chemotherapeutic agents are of limited benefit in patients with recurrent or metastatic cancer of the esophagus or gastroesophageal junction (GEJ). We report results from a phase II trial in this population using gefitinib, an oral epidermal growth factor receptor inhibitor. Patients and methods Eligibility required a diagnosis of esophageal or GEJ adenocarcinoma or squamous cell carcinoma, which was either metastatic or recurrent and incurable after initial therapy. No more than one prior chemotherapy regimen was permitted. Treatment consisted of gefitinib 250 mg daily for a minimum of 8 weeks. Results Between April 2003 and January 2010, 58 patients, including 18 who were chemotherapy-naive, were entered into this trial. Toxicity was modest, although most experienced grade 1–2 diarrhea and/or skin rash. There were 4 partial responders (7%) and 10 patients with stable disease (17%). The clinical benefit (partial response and stable disease) lasted for a median 6.1 months. Median survival for all patients was 5.5 months with survival projections at 1-year of 24.6% and at 2-years of 12.5%. Conclusion Gefitinib was well tolerated but of limited efficacy in patients with recurrent or metastatic esophageal or GEJ cancer. Further study of this or similar agents will require better patient selection.

45 citations


Journal ArticleDOI
TL;DR: Esophageal/esophagogastric junction cancer staging in the AJCC staging manual is data driven and harmonized with gastric staging, and new definitions are Tis, T4, regional lymph node, N, and M.

32 citations


Journal ArticleDOI
TL;DR: Results from the multilevel models suggest numeric versus symbolic prices decreased the likelihood of choosing the lowest cost plan, suggesting that decision cues operated independently and collectively when selecting a drug plan.
Abstract: Because many seniors choose Medicare Part D plans offering poorer coverage at greater cost, the authors examined the effect of price frames, brand names, and choice set size on participants’ abilit...

29 citations


Journal ArticleDOI
TL;DR: A common histomorphologic pattern of esophageal carcinoma cuniculatum is identified and supports the fact that surgical resection of the tumor by esophagectomy provides long-term survival even in patients with T3 tumor.
Abstract: Carcinoma cuniculatum, a unique variant of well-differentiated squamous cell carcinoma, has been only rarely reported in the esophagus. We report 9 cases of esophageal carcinoma cuniculatum diagnosed on esophagectomy specimens in 7 men and 2 women during a 20-year period. All but 1 of the patients presented with persistent or progressive dysphagia. All patients had an esophageal mass or lesion on endoscopic examination. In 8 cases (88.8%), the tumor was located in the distal esophagus. Burrowing was noted on the tumor surface in 2 recent cases on macroscopic examination. All carcinomas were invasive either at the mucosa (n=2), submucosa (n=1), muscularis propria (n=4), adventitia (n=3), or adventitia and lung (n=1). All carcinomas demonstrated a common histologic pattern characterized by hyperkeratosis, acanthosis, dyskeratosis, abnormal keratinization, keratin-filled cyst/furrows, koilocyte-like cells, intraepithelial neutrophils, and focal cytologic atypia. In situ hybridization for human papillomavirus subtypes was negative in all 10 tumors tested. None of the cases showed lymph node metastasis. Two patients died postoperatively due to complications. The remaining patients were followed up for a median duration of 84 months (48 to 214 mo). During the follow-up period, 3 patients died 49, 66, and 214 months after esophagectomy at the ages of 66, 68, and 91 years, respectively; death in these 3 cases was not related to recurrence/metastases of esophageal cancer. Four patients were alive without disease at 48, 49, 84, and 87 months after curative resection. Our report identifies a common histomorphologic pattern of esophageal carcinoma cuniculatum and supports the fact that surgical resection of the tumor by esophagectomy provides long-term survival even in patients with T3 tumor.

29 citations


Journal ArticleDOI
TL;DR: In conclusion, the CC and UM systems show excellent agreement and define histologic categories that can improve prediction of adenocarcinoma on resection.
Abstract: Distinguishing Barrett esophagus with high-grade dysplasia (BE-HGD) from intramucosal and submucosal adenocarcinomas on biopsies is challenging, yet important, in the choice of therapy. The current study evaluates preresection biopsies from patients who underwent esophagectomy for at least BE-HGD, to compare the recently published histologic categories by the University of Michigan (UM) and Cleveland Clinic (CC), correlate preresection and final resection diagnosis, and identify histologic features in biopsies that might be predictive of adenocarcinoma on esophagectomy. A total of 112 cases with a consensus biopsy diagnosis (agreement by ≥4 of 7 gastrointestinal pathologists) were statistically analyzed to identify histologic features that predicted adenocarcinoma on resection. Applying the UM criteria to the biopsy series showed excellent agreement with the CC system (κ=0.86) and significant correlation between preoperative and esophagectomy diagnoses (P 1 focus of single-cell infiltration into the lamina propria (OR, 8.9; P<0.001) increased the odds of finding carcinoma on resection. The latter 2 variables remained independent predictors of adenocarcinoma in multivariable analysis. In conclusion, the CC and UM systems show excellent agreement and define histologic categories that can improve prediction of adenocarcinoma on resection.

20 citations


Journal ArticleDOI
TL;DR: The study uses the hospital admissions section as a source of data and addresses the long-debated but unanswered question, “Does MIE lead to a superior outcome compared with open esophagectomy?"
Abstract: T he Hospital Episode Database (HED) is a national statistical data warehouse of the English National Health Services Trusts. The study by Mamidanna and colleagues,1 published in this issue of Annals of Surgery, uses the hospital admissions section as a source of data. These administrative data provide interesting insight into the practice of esophagectomy. During a 4-year period ending in April 2009, 7502 patients underwent esophagectomy for cancer. The majority, 84.6%, received a conventional (open) esophagectomy; the minority, 15.4%, received a minimally invasive esophagectomy (MIE). However, the frequency of MIE quadrupled over the study period, with 25% of patients having a MIE in the last year of study. The distribution of MIE was not uniform among the Trusts or surgeons. The authors should be commended for their endeavor to assess short-term outcome in this group of patients. They address the long-debated but unanswered question, “Does MIE lead to a superior outcome compared with open esophagectomy?”

7 citations




Journal ArticleDOI
TL;DR: The data supporting current management strategies is outlined, and the ability to preserve the esophagus with endoscopic mucosal ablation or resection and reduce morbidity of treatment has made endoscopic treatment the mainstay of therapy.

2 citations