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Featured researches published by S.E. James.


Radiotherapy and Oncology | 2017

Multi-institutional analysis of radiation modality use and postoperative outcomes of neoadjuvant chemoradiation for esophageal cancer

Steven H. Lin; K.W. Merrell; Jincheng Shen; Vivek Verma; Arlene M. Correa; Lu Wang; Peter F. Thall; Neha Bhooshan; S.E. James; Michael G. Haddock; Mohan Suntharalingam; Minesh P. Mehta; Zhongxing Liao; James D. Cox; Ritsuko Komaki; Reza J. Mehran; Michael D. Chuong; Christopher L. Hallemeier

PURPOSE Relative radiation dose exposure to vital organs in the thorax could influence clinical outcomes in esophageal cancer (EC). We assessed whether the type of radiation therapy (RT) modality used was associated with postoperative outcomes after neoadjuvant chemoradiation (nCRT). PATIENTS AND METHODS Contemporary data from 580 EC patients treated with nCRT at 3 academic institutions from 2007 to 2013 were reviewed. 3D conformal RT (3D), intensity modulated RT (IMRT) and proton beam therapy (PBT) were used for 214 (37%), 255 (44%), and 111 (19%) patients, respectively. Postoperative outcomes included pulmonary, GI, cardiac, wound healing complications, length of in-hospital stay (LOS), and 90-day postoperative mortality. Cox model fits, and log-rank tests both with and without Inverse Probability of treatment Weighting (IPW) were used to correct for bias due to non-randomization. RESULTS RT modality was significantly associated with the incidence of pulmonary, cardiac and wound complications, which also bore out on multivariate analysis. Mean LOS was also significantly associated with treatment modality (13.2days for 3D (95%CI 11.7-14.7), 11.6days for IMRT (95%CI 10.9-12.7), and 9.3days for PBT (95%CI 8.2-10.3) (p<0.0001)). The 90day postoperative mortality rates were 4.2%, 4.3%, and 0.9%, respectively, for 3D, IMRT and PBT (p=0.264). CONCLUSIONS Advanced RT technologies (IMRT and PBT) were associated with significantly reduced rate of postoperative complications and LOS compared to 3D, with PBT displaying the greatest benefit in a number of clinical endpoints. Ongoing prospective randomized trial will be needed to validate these results.


Journal of Thoracic Oncology | 2017

Utility of 18F-FDG PET for Predicting Histopathologic Response in Esophageal Carcinoma following Chemoradiation

Andrea L. Arnett; K.W. Merrell; Erica Martin Macintosh; S.E. James; Mark A. Nathan; K. Robert Shen; Karthik Ravi; Michelle A. Neben Wittich; Michael G. Haddock; Christopher L. Hallemeier

Introduction: For patients with esophageal cancer undergoing neoadjuvant chemoradiation (CRT) followed by surgical resection, complete histopathologic response (pCR) is associated with favorable overall survival (OS). The aim of this study was to evaluate the correlation between 18F‐fluorodeoxyglucose positron emission tomography (FDG PET) response to neoadjuvant CRT and pCR. Methods: Maximum standardized uptake values and standardized uptake ratios (SURs) were measured before and after CRT. SUR was normalized to liver uptake and mediastinal blood pool uptake. FDG PET complete response was defined as metabolic activity normalization to hepatic and blood pool activity. The correlation between FDG PET parameters and pCR was examined through logistic regression analyses. Results: In total, 193 patients were monitored for a median of 3.6 years after initiation of CRT. Most tumors were adenocarcinoma (85%) and stage T3 (75%). Complete FDG PET response and pCR occurred in 27% and 34% of patients, respectively. Histologic findings, chemotherapy type, tumor stage, and radiation dose were not significantly associated with complete radiographic response. The rates of pCR in patients with and without radiographic complete response were 42% and 31% (p = 0.17), respectively. No predictive correlation was found between pCR and change in maximum standardized uptake value (p = 0.25), in SUR normalized to blood pool uptake (p = 0.20), or in SUR normalized to liver uptake (p = 0.15). The 5‐year OS rate was 46% for patients with a complete FDG PET response versus 44% without a complete response (p = 0.78). The 5‐year OS rate of patients who achieved pCR was 49% versus 43% for patients with residual tumor (p = 0.04). Conclusion: For patients with esophageal cancer who received neoadjuvant chemoradiation, pretreatment and posttreatment FDG PET parameters did not correlate with pCR or OS.


Journal of Clinical Oncology | 2016

Outcomes and toxicity in patients treated with bimodality or trimodality therapy for esophageal carcinoma with intensity modulated radiation therapy (IMRT).

Ajay B. Patel; Stephen J. Ko; S.E. James; Jonathan B. Ashman; William G. Rule; Corey James Hobbs; Christopher L. Hallemeier; Emily R. Brennan; Michael G. Heckman; Katherine S. Tzou; Laura A. Vallow; Jennifer L. Peterson; Rob Miller; Steven J. Buskirk

88 Background: There is not yet a consensus on the efficacy and safety of IMRT for the treatment of patients with esophageal carcinomas. We report on our experience with outcomes and toxicity with IMRT for these patients. Methods: Fifty-five patients with esophageal carcinoma were treated with IMRT at our institution from 12/2008 and 12/2014. Medical records were retrospectively reviewed. All patients received concurrent chemotherapy (majority 5-FU with oxaliplatin). Thirty-one (56%) patients underwent surgery. Fifty (91%) received 50.4 Gy in 28 fractions. Seventy-three percent of cases were adenocarcinoma. Regions include mid-thoracic (15%), lower thoracic (64%), and GE junction (22%). Clinical uT-stages were as follows: T1 (2%), T2 (20%), T3 (69%), and T4a (5%). Clinical N-stages were as follows: N0 (33%), N1 (53%), N2 (13%), and N3 (2%). Results: Median follow-up for all patients was 15 months (1.5 - 64.5) and 25.5 months (1.5 - 64.5) for patients who were alive at follow-up (n = 31). Fifty-one (93%) p...


Clinical Breast Cancer | 2016

Inflammatory TNBC Breast Cancer: Demography and Clinical Outcome in a Large Cohort of Patients With TNBC.

Tithi Biswas; Jimmy T. Efird; Shreya Prasad; S.E. James; Paul R. Walker; Timothy M. Zagar


International Journal of Radiation Oncology Biology Physics | 2017

A Multi-institutional Analysis of Trimodality Therapy for Esophageal Cancer in Elderly Patients

S.C. Lester; Steven H. Lin; Michael Chuong; Neha Bhooshan; Zhongxing Liao; Andrea L. Arnett; S.E. James; Jaden D. Evans; Grant M. Spears; Ritsuko Komaki; Michael G. Haddock; Minesh P. Mehta; Christopher L. Hallemeier; K.W. Merrell


Journal of Clinical Oncology | 2017

Insurance status as a strong predictor of outcome in triple-negative breast cancer (TNBC): A multi-institutional retrospective study.

Tithi Biswas; Shreya Prasad; Timothy M. Zagar; Jimmy T. Efird; S.E. James; Paul R. Walker; Rachel Elizabeth Raab; Lisa A. Carey; Lawrence B. Marks


International Journal of Radiation Oncology Biology Physics | 2017

Poster ViewingIs Pathological Complete Response Rate Associated with Improved Local Control in Localized Triple Negative Breast Cancer After Neoadjuvant Chemotherapy

Tithi Biswas; Jimmy T. Efird; Shreya Prasad; S.E. James; Timothy M. Zagar


SpringerPlus | 2016

Failure patterns and survival outcomes in triple negative breast cancer (TNBC): a 15 year comparison of 448 non-Hispanic black and white women

Shreya Prasad; Jimmy T. Efird; S.E. James; Paul R. Walker; Timothy M. Zagar; Tithi Biswas


Journal of Clinical Oncology | 2016

Inflammatory TNBC breast cancer: demography and clinical outcome in a large cohort of TNBC patients

Tithi Biswas; Jimmy T. Efird; Paul R. Walker; S.E. James; Shreya Prasad; Timothy M. Zagar


International Journal of Radiation Oncology Biology Physics | 2016

Outcomes and Toxicity in Patients Treated With Intensity Modulated Radiation Therapy (IMRT) for Esophageal Carcinoma

Ajay B. Patel; S.E. James; Michael G. Heckman; E. Vargas; Corey James Hobbs; William G. Rule; Christopher L. Hallemeier; Robert C. Miller; Jonathan B. Ashman; Stephen J. Ko

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Jimmy T. Efird

East Carolina University

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Shreya Prasad

University of North Carolina at Chapel Hill

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Timothy M. Zagar

University of North Carolina at Chapel Hill

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Tithi Biswas

Case Western Reserve University

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Paul R. Walker

East Carolina University

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