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Featured researches published by Xiangyu Cong.


Journal of The American College of Surgeons | 2013

Surgical Residency and Attrition: Defining the Individual and Programmatic Factors Predictive of Trainee Losses

Michael C. Sullivan; Heather Yeo; Sanziana A. Roman; Maria M. Ciarleglio; Xiangyu Cong; Richard H. Bell; Julie Ann Sosa

BACKGROUND Voluntary resident attrition remains problematic despite recent changes in postgraduate general surgery training, including reduction of work hours. STUDY DESIGN We conducted a prospective study of all postgraduate year (PGY)-1 and -2 trainees on the 2008 American Board of Surgery resident roster (ABS-RR) who completed the National Study of Expectations and Attitudes of Residents in Surgery (NEARS) survey after the American Board of Surgery In-Training Examination (ABSITE) in 2008 or 2009. RESULTS Among 2,222 PGY-1 and -2 residents on the 2008 ABS-RR, 2,033 completed the NEARS survey in 2008 or 2009 (91.5%). The only demographic or programmatic variables associated with voluntary attrition on univariate analysis were PGY-1 status (9.4% risk vs 4.5% risk for PGY-2, p < 0.001) and program location (p = 0.03). Response differences (p < 0.01) were noted in 23 survey items. In multivariate modeling, PGY-2 status was protective against voluntary attrition (p < 0.001, hazard ratio [HR] 0.41), while programs located outside of the South (Northeast: p = 0.006, HR 2.39; Midwest: p = 0.01, HR 2.37; West: p = 0.10, HR 1.76) were associated with higher attrition. The attrition group more frequently reported that they had considered leaving training (p < 0.001, HR 2.59), that the personal cost of training was too great (p < 0.001, HR 2.89), that they were dissatisfied with their operative experience (p = 0.002, HR 1.89), and that they were not committed to completing their training (p < 0.001, HR 3.96). Using the estimated regression coefficient for each variable in the multivariate models, we calculated a risk score for individual residents; these scores were used to construct covariate-adjusted survivorship functions. CONCLUSIONS Resident attitudes, PGY-1 status, and program location are most frequently associated with voluntary attrition. Our risk score calculation represents a novel potential tool for programs to quantify deficiencies in the training experience of residents, and develop targeted strategies to limit disaffection and improve resident retention.


British Journal of Cancer | 2016

Final analysis of a phase II study of modified FOLFIRINOX in locally advanced and metastatic pancreatic cancer.

Stacey Stein; Edward Samuel James; Yanhong Deng; Xiangyu Cong; Jeremy S. Kortmansky; Jia Li; Carol Staugaard; Doddamane Indukala; Ann Marie Boustani; Vatsal Patel; Charles Cha; Ronald R. Salem; B.W. Chang; Howard S. Hochster; Jill Lacy

Background:Modifications of FOLFIRINOX are widely used despite the absence of prospective data validating efficacy in metastatic disease (metastatic pancreatic cancer (MPC)) or locally advanced pancreatic cancer (LAPC). We conducted a multicentre phase II study of modified FOLFIRINOX in advanced pancreatic cancer to assess the impact of dose attenuation in MPC and efficacy in LAPC.Methods:Patients with untreated MPC or LAPC received modified FOLFIRINOX (irinotecan and bolus 5-fluorouracil reduced by 25%). Adverse events (AEs) were compared with full-dose FOLFIRINOX. Response rate (RR), median progression-free survival (PFS) and median overall survival (OS) were determined.Results:In total, 31 and 44 patients with LAPC and MPC were enrolled, respectively. In MPC, efficacy of modified FOLFIRINOX was comparable with FOLFIRINOX with RR 35.1%, OS 10.2 months (95% CI 7.65–14.32) and PFS 6.1 months (95% CI 5.19–8.31). In LAPC, efficacy was notable with RR 17.2%, resection rate 41.9%, PFS 17.8 months (95% CI 11.0–23.9) and OS 26.6 months (95% CI 16.7, NA). Neutropenia (P<0.0001), vomiting (P<0.001) and fatigue (P=0.01) were significantly decreased. [18F]-Fluorodeoxyglucose positron emission tomography imaging response did not correlate with PFS or OS.Conclusions:In this first prospective study of modified FOLFIRINOX in MPC and LAPC, we observed decreased AEs compared with historical control patients. In MPC, the efficacy appears comparable with FOLFIRINOX. In LAPC, PFS and OS were prolonged and support the continued use of FOLFIRINOX in this setting.


The Annals of Thoracic Surgery | 2012

Model for End-Stage Liver Disease Score Predicts Adverse Events Related to Ventricular Assist Device Therapy

Pramod Bonde; Natalie C. Ku; Elizabeth A. Genovese; C. Bermudez; J.K. Bhama; Maria M. Ciarleglio; Xiangyu Cong; Jeffrey J. Teuteberg; Robert L. Kormos

BACKGROUND The Model for End-stage Liver Disease (MELD) score is a marker of multisystem organ dysfunction. It has been used to predict outcomes in patients undergoing hepatic and nonhepatic interventions. End-stage heart disease exhibits a varying degree of multiorgan dysfunction, which impacts the adverse events related to ventricular assist device (VAD) therapy. Our aim for the present study was to investigate the value of MELD score in predicting adverse events related with VAD therapy. METHODS Data were collected on demographics, clinical characteristics, MELD score; Interagency Registry for Mechanically Assisted Circulatory Support-defined VAD adverse events within the first 6 months, and survival from VAD recipients (n=286; from 1996 to 2009). Univariable, multivariable, and Cox regression analyses were performed using SAS software (SAS Institute, Cary, NC). RESULTS The mean MELD score was 14.4±5.9. Actuarial incidence of infections, bleeding events, and cardiovascular dysfunction at 6 months was 65.4%, 52.1%, and 45.6%, respectively. Multivariable Cox proportional hazards model (controlling for gender, type of device, diagnosis, intention to treat, urgency, and inotropic use) confirmed that MELD score predicted mortality, respiratory, and renal dysfunction at 6 months (p<0.01). CONCLUSIONS Preoperative MELD score is predictive of mortality, respiratory, and renal dysfunction at 6 months after controlling for gender, type of device, diagnosis, intention to treat, urgency, and inotropic use. The MELD score may be used as a quantitative tool to assess the adverse events associated with VAD therapy.


Laryngoscope | 2013

Parotid gland lymphoma: Prognostic analysis of 2140 patients

Aaron J. Feinstein; Maria M. Ciarleglio; Xiangyu Cong; Michael D. Otremba; Benjamin L. Judson

Assess the demographic, clinical, and pathologic features of patients with parotid gland lymphoma and their prognostic importance using US population‐based data.


Journal of the American Geriatrics Society | 2016

Ten-Year Prevalence and Incidence of Urinary Incontinence in Older Women: A Longitudinal Analysis of the Health and Retirement Study.

Elisabeth A. Erekson; Xiangyu Cong; Mary K. Townsend; Maria M. Ciarleglio

To measure the incidence of urinary incontinence (UI) over 10 years in older women who did not report UI at baseline in 1998, to estimate the prevalence of female UI according to severity and type, and to explore potential risk factors for development of UI.


Medical Oncology | 2013

FOLFIRINOX for locally advanced and metastatic pancreatic cancer: single institution retrospective review of efficacy and toxicity

Krishna S. Gunturu; Xiaopan Yao; Xiangyu Cong; Jaykumar Thumar; Howard S. Hochster; Stacey Stein; Jill Lacy


Journal of Clinical Oncology | 2015

Final analysis of a phase II study of Yale-modified FOLFIRINOX (mFOLFIRINOX) in metastatic pancreatic cancer (MPC).

Edward Samuel James; Xiangyu Cong; Xiaopan Yao; Carol A. Hahn; Kristin Kaley; Jia Li; Jeremy S. Kortmansky; Neal A. Fischbach; Charles Cha; Ronald R. Salem; Stacey Stein; Howard S. Hochster; Jill Lacy


Journal of Gastrointestinal Surgery | 2012

Comprehensive Analysis of Variables Affecting Delayed Gastric Emptying Following Pancreaticoduodenectomy

John W. Kunstman; Annabelle L. Fonseca; Maria M. Ciarleglio; Xiangyu Cong; Abby Hochberg; Ronald R. Salem


Journal of Clinical Oncology | 2014

Interim analysis of a phase II study of dose-modified FOLFIRINOX (mFOLFIRINOX) in locally advanced (LAPC) and metastatic pancreatic cancer (MPC).

Edward Samuel James; Xiaopan Yao; Xiangyu Cong; Jia Li; Carol A. Hahn; Kristin Kaley; Jeremy S. Kortmansky; Neal A. Fischbach; B.W. Chang; Ronald R. Salem; Charles Cha; Stacey Stein; Howard S. Hochster; Jill Lacy


Journal of Clinical Oncology | 2012

Single institution experience with FOLFIRINOX in advanced pancreatic cancer (PC).

Krishna S. Gunturu; Jaykumar Thumar; Howard S. Hochster; Stacey Stein; Xiaopan Yao; Xiangyu Cong; Carol A. Hahn; Kristin Kaley; Jill Lacy

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Jeremy S. Kortmansky

Memorial Sloan Kettering Cancer Center

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