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Featured researches published by Gavitt Woodard.


Archives of Surgery | 2012

Laparoscopic vs Open Gastric Bypass Surgery: Differences in Patient Demographics, Safety, and Outcomes

Gaurav Banka; Gavitt Woodard; Tina Hernandez-Boussard; John M. Morton

OBJECTIVE To determine national outcome differences between laparoscopic Roux-en-Y gastric bypass (LRYGB) and open Roux-en-Y gastric bypass (ORYGB). DESIGN Retrospective cohort study. SETTING The Nationwide Inpatient Sample. PATIENTS Patients undergoing ORYGB and LRYGB. MAIN OUTCOME MEASURES Outcome measures were number of procedures performed, patient and hospital characteristics, patient complications, mortality, length of stay, resource use, and Agency for Healthcare Research and Quality Patient Safety Indicators. Both demographic and outcomes variables were compared by either t test or χ2 analysis, with regression analysis adjusting for confounding variables. RESULTS The ORYGB and LRYGB cohorts consisted of 41 094 and 115 177 cases, respectively. From 2005 to 2007, LRYGB was more commonly performed than ORYGB (72% vs 28%; P < .001) and at high-volume hospitals (69% vs 61%; P < .001). A higher percentage of ORYGB compared with LRYGB patients were Medicare (9.3% vs 7.1%) and Medicaid (10.4% vs 5.9%; P < .01) beneficiaries. More ORYGB patients compared with LRYGB patients were discharged with nonroutine dispositions (7.7% vs 2.4%; P = .005), died (0.2% vs 0.1%; P < .001), and had 1 or more complications (18.7% vs 12.3%; P < .001). All Patient Safety Indicator rates were higher for ORYGB. Patients who had ORYGB compared with LRYGB also had longer median lengths of stay (3.5 vs 2.4 days; P < .001) and higher total charges (


Journal of Thoracic Oncology | 2016

Consensus Report of the 2015 Weinman International Conference on Mesothelioma

Michele Carbone; Shreya Kanodia; Ann Chao; Aubrey Miller; Anil Wali; David N. Weissman; Alex A. Adjei; Francine Baumann; Paolo Boffetta; Brenda J. Buck; Marc de Perrot; A. Umran Dogan; Alessandro F. Gualtieri; Raffit Hassan; Mary Hesdorffer; Fred R. Hirsch; David E. Larson; Weimin Mao; Scott A. Masten; Harvey I. Pass; Julian Peto; Enrico Pira; Ian M. Steele; Anne Tsao; Gavitt Woodard; Haining Yang; Shakun Malik

35 018 vs


Journal of The American College of Surgeons | 2012

Normal Alcohol Metabolism after Gastric Banding and Sleeve Gastrectomy: A Case-Cross-Over Trial

Eric Changchien; Gavitt Woodard; Tina Hernandez-Boussard; John M. Morton

32 671; P < .001). Patients who had LRYGB had a lower odds ratio than patients who had ORYGB for both mortality (odds ratio, 0.54; P < .001) and having 1 or more complications (odds ratio, 0.66; P < .001) even after adjusting for confounding variables. CONCLUSION In this population-based study, LRYGB provided greater safety than ORYGB even after adjusting for patient-level socioeconomic and comorbidity differences.


British Journal of Surgery | 2012

Effect of Roux-en-Y gastric bypass on testosterone and prostate-specific antigen

Gavitt Woodard; Shushmita Ahmed; V. Podelski; Tina Hernandez-Boussard; J. Presti; John M. Morton

ABSTRACT On November 9 and 10, 2015, the International Conference on Mesothelioma in Populations Exposed to Naturally Occurring Asbestiform Fibers was held at the University of Hawaii Cancer Center in Honolulu, Hawaii. The meeting was cosponsored by the International Association for the Study of Lung Cancer, and the agenda was designed with significant input from staff at the U.S. National Cancer Institute and National Institute of Environmental Health Sciences. A multidisciplinary group of participants presented updates reflecting a range of disciplinary perspectives, including mineralogy, geology, epidemiology, toxicology, biochemistry, molecular biology, genetics, public health, and clinical oncology. The group identified knowledge gaps that are barriers to preventing and treating malignant mesothelioma (MM) and the required next steps to address barriers. This manuscript reports the groups efforts and focus on strategies to limit risk to the population and reduce the incidence of MM. Four main topics were explored: genetic risk, environmental exposure, biomarkers, and clinical interventions. Genetics plays a critical role in MM when the disease occurs in carriers of germline BRCA1 associated protein 1 mutations. Moreover, it appears likely that, in addition to BRCA1 associated protein 1, other yet unknown genetic variants may also influence the individual risk for development of MM, especially after exposure to asbestos and related mineral fibers. MM is an almost entirely preventable malignancy as it is most often caused by exposure to commercial asbestos or mineral fibers with asbestos‐like health effects, such as erionite. In the past in North America and in Europe, the most prominent source of exposure was related to occupation. Present regulations have reduced occupational exposure in these countries; however, some people continue to be exposed to previously installed asbestos in older construction and other settings. Moreover, an increasing number of people are being exposed in rural areas that contain noncommercial asbestos, erionite, and other mineral fibers in soil or rock (termed naturally occurring asbestos [NOA]) and are being developed. Public health authorities, scientists, residents, and other affected groups must work together in the areas where exposure to asbestos, including NOA, has been documented in the environment to mitigate or reduce this exposure. Although a blood biomarker validated to be effective for use in screening and identifying MM at an early stage in asbestos/NOA‐exposed populations is not currently available, novel biomarkers presented at the meeting, such as high mobility group box 1 and fibulin‐3, are promising. There was general agreement that current treatment for MM, which is based on surgery and standard chemotherapy, has a modest effect on the overall survival (OS), which remains dismal. Additionally, although much needed novel therapeutic approaches for MM are being developed and explored in clinical trials, there is a critical need to invest in prevention research, in which there is a great opportunity to reduce the incidence and mortality from MM.


Oncotarget | 2016

Whole exome and targeted deep sequencing identify genome- wide allelic loss and frequent SETDB1 mutations in malignant pleural mesotheliomas

Hio Chung Kang; Hong Kwan Kim; Sharon Lee; Pedro Mendez; James Wansoo Kim; Gavitt Woodard; Jun-Hee Yoon; Kuang-Yu Jen; Li Tai Fang; Kirk D. Jones; David M. Jablons; Il-Jin Kim

BACKGROUND Severe obesity remains the leading public health concern of the industrialized world, with bariatric surgery as the only current effective enduring treatment. In addition to gastric bypass, gastric banding and sleeve gastrectomy have emerged as viable treatment options for the severely obese. Occasionally, poor postoperative psychological adjustment has been reported. It has been previously demonstrated that breath alcohol content (BAC) levels and time to sober were increased in postoperative gastric bypass patients. The aim of this study was to examine whether alcohol metabolism in patients undergoing restrictive-type bariatric procedures is also altered. STUDY DESIGN Nine patients undergoing laparoscopic adjustable gastric banding (LAGB) and 7 patients undergoing laparoscopic sleeve gastrectomy (LSG) were recruited. Preoperatively, 3-month and 6-month BAC and time to sober were measured after administration of 5 ounces of red wine. In addition, participants were asked to complete a questionnaire of drinking habits. RESULT The 16 total participants achieved a mean 44.7% 6-month excess weight loss. There were no significant changes in peak BAC or time to sober from preoperative levels (0.033%, 67.8 min, respectively) to 3 months (0.032%, 77.1 min, respectively, p = 0.421) or 6 months (0.035%, 81.2 min, respectively, p = 0.198). CONCLUSION Patients undergoing LAGB and LSG do not share the same altered alcohol metabolism as seen in gastric bypass patients. However, all bariatric surgery patients should be counseled regarding alcohol use.


Translational lung cancer research | 2017

Drug development against the hippo pathway in mesothelioma

Gavitt Woodard; Yi-Lin Yang; Liang You; David M. Jablons

Obese men have lower serum levels of testosterone, dehydroepiandrosterone (DHEA) and prostate‐specific antigen (PSA), but an increased risk of dying from prostate cancer. The aim of this study was to examine the effect of surgically induced weight loss on serum testosterone, DHEA and PSA levels in obese men.


Thoracic Cancer | 2016

Significance of different response evaluation criteria in predicting progression-free survival of lung cancer with certain imaging characteristics

Dengxia Yang; Gavitt Woodard; Chan Zhou; Xinyue Wang; Zhujun Liu; Zhaoxiang Ye; Kai Li

Malignant pleural mesothelioma (MPM), a rare malignancy with a poor prognosis, is mainly caused by exposure to asbestos or other organic fibers, but the underlying genetic mechanism is not fully understood. Genetic alterations and causes for multiple primary cancer development including MPM are unknown. We used whole exome sequencing to identify somatic mutations in a patient with MPM and two additional primary cancers who had no evidence of venous, arterial, lymphovascular, or perineural invasion indicating dissemination of a primary lung cancer to the pleura. We found that the MPM had R282W, a key TP53 mutation, and genome-wide allelic loss or loss of heterozygosity, a distinct genomic alteration not previously described in MPM. We identified frequent inactivating SETDB1 mutations in this patient and in 68 additional MPM patients (mutation frequency: 10%, 7/69) by targeted deep sequencing. Our observations suggest the possibility of a new genetic mechanism in the development of either MPM or multiple primary cancers. The frequent SETDB1 inactivating mutations suggest there could be new diagnostic or therapeutic options for MPM.


Oncotarget | 2016

Gli promotes epithelial-mesenchymal transition in human lung adenocarcinomas

Hui Li; Dongsheng Yue; Joy Q. Jin; Gavitt Woodard; Bhairavi Tolani; Thomas M. Luh; Etienne Giroux-Leprieur; Minli Mo; Zhao Chen; Juanjuan Che; Zhenfa Zhang; Yong Zhou; Lei Wang; Xishan Hao; David M. Jablons; Changli Wang; Biao He

Advances in the treatments for malignant pleural mesothelioma (MPM) have been disappointing until recently. Conventional cytotoxic drugs fail in MPM in part because they do not address the cancer stem cell population or stem cell pathways that drive tumor resistance and resurgence following treatment. The Hippo stem cell pathway regulates cell contact inhibition with tumor suppressor genes such as NF2 (Neurofibromatosis 2) upstream controlling YAP (Yes-associated protein 1) oncogenes. NF2 is mutated in 40-50% of all MPM and downstream YAP is constitutively active in greater than 70% of MPM, making the downstream YAP/TEAD (transcriptional enhancer associate domain) complex the ultimate target. Novel small molecule YAP inhibitors are showing promising results in preclinical studies and may prove to be effective chemotherapy drugs in MPM.


Journal of Surgical Oncology | 2016

Hybrid minimally invasive Ivor Lewis esophagectomy after neoadjuvant chemoradiation yields excellent long-term survival outcomes with minimal morbidity.

Gavitt Woodard; Jane Crockard; Carolyn Clary-Macy; Clara Zoon-Besselink; Kirk D. Jones; Wolfgang Michael Korn; Andrew H. Ko; Alexander Gottschalk; Stanley J. Rogers; David M. Jablons

Certain radiographic signs of a treatment response, such as cavitation, changes in density, or tumor change along a short axis, are not considered by Response Evaluation Criteria in Solid Tumors (RECIST). This study evaluates what additional prognostic information can be obtained by including these criteria in tumor assessment.


PLOS ONE | 2015

EMX2 Is a Predictive Marker for Adjuvant Chemotherapy in Lung Squamous Cell Carcinomas.

Dongsheng Yue; Hui Li; Juanjuan Che; Yi Zhang; Bhairavi Tolani; Minli Mo; Hua Zhang; Qingfeng Zheng; Yue Yang; Runfen Cheng; Joy Q. Jin; Thomas W. Luh; Cathryn Yang; Hsin Hui K. Tseng; Etienne Giroux-Leprieur; Gavitt Woodard; Xishan Hao; Changli Wang; David M. Jablons; Biao He

Adenocarcinoma is the most common type of lung cancer. Epithelial-mesenchymal transition (EMT) is required for tumor invasion/metastasis and the components that control this process are potential therapeutic targets. This study we examined the role of Gli in lung adenocarcinoma and whether its activation regulates metastasis through EMT in lung adenocarcinoma. We found that tumors with high Gli expression had significantly lower E-Cadherin expression in two independent cohorts of patients with lung adenocarcinoma that we studied. In vitro up-regulation of SHh resulted in increased cell migration while small molecule inhibitors of Smo or Gli significantly reduced cell mobility both in a wound healing assay and in a 3D cell invasion assay. Inhibition of Gli in vivo decreased tumor growth and induced an increase in E-Cadherin expression. Our results indicate that Gli may be critical for lung adenocarcinoma metastasis and that a novel Gli inhibitor shows promise as a therapeutic agent by preventing cell migration and invasion in vitro and significantly reducing tumor growth and increasing E-Cadherin expression in vivo.

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Kirk D. Jones

University of California

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Il-Jin Kim

University of California

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