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Dive into the research topics where Glenn E. Peters is active.

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Featured researches published by Glenn E. Peters.


Head and Neck-journal for The Sciences and Specialties of The Head and Neck | 1999

T1 and T2 squamous cell carcinoma of the oral tongue: prognostic factors and the role of elective lymph node dissection.

Samuel W. Beenken; Helen Krontiras; William A. Maddox; Glenn E. Peters; Seng-jaw Soong; Marshall M. Urist

The management of micrometastatic disease from squamous cell carcinoma (SCC) of the oral tongue remains controversial. This study describes prognostic factors in the disease and reviews the role of elective neck dissection (END).


Laryngoscope | 2007

Free tissue transfer to manage salvage laryngectomy defects after organ preservation failure

Kirk P. Withrow; Eben L. Rosenthal; Christine G. Gourin; Glenn E. Peters; J. Scott Magnuson; David J. Terris; William W. Carroll

Objective: Salvage laryngectomy to treat organ preservation failures results in significantly higher local wound complications. Even in the absence of extralaryngeal disease, primary closure of laryngeal defects can result in protracted wound care problems. We hypothesize that even when sufficient mucosa is present to close the defect primarily, introduction of vascularized tissue to close the defect may improve outcomes.


International Journal of Radiation Oncology Biology Physics | 2008

Locoregionally Advanced Head and Neck Cancer Treated With Primary Radiotherapy: A Comparison of the Addition of Cetuximab or Chemotherapy and the Impact of Protocol Treatment

Jimmy J. Caudell; Stephen M. Sawrie; S.A. Spencer; Renee A. Desmond; William R. Carroll; Glenn E. Peters; Lisle Nabell; Ruby F. Meredith; James A. Bonner

PURPOSE The addition of platinum-based chemotherapy (ChRT) or cetuximab (ExRT) to concurrent radiotherapy (RT) has resulted in improved survival in Phase III studies for locoregionally advanced head and neck cancer (LAHNC). However the optimal treatment regimen has not been defined. A retrospective study was performed to compare outcomes in patients who were treated definitively with ExRT or ChRT. METHODS Cetuximab with concurrent RT was used to treat 29 patients with LAHNC, all of whom had tumors of the oral cavity, oropharynx, or larynx. All patients were T2 to T4 and overall American Joint Committee on Cancer Stage III to IVB, with a Karnofsky Performance Status (KPS) score of 60 or greater. ChRT was used to treat 103 patients with similar characteristics. Patients were evaluated for locoregional control (LRC), distant metastasis-free survival (DMFS), disease-specific survival (DSS), and overall survival (OS). Median follow-up for patients alive at last contact was 83 months for those treated with ExRT and 53 months for those treated with ChRT. Cox proportional hazard models were used to assess independent prognostic factors. RESULTS The LRC, DMFS, and DSS were not significantly different, with 3-year rates of 70.7%, 92.4%, and 78.6% for ExRT and 74.7%, 86.6%, and 76.5% for ChRT, respectively. The OS was significantly different between the two groups (p = 0.02), with 3-year rates of 75.9% for ExRT and 61.3% for ChRT. OS was not significant when patients who were on protocol treatments of ExRT or ChRT were compared. Also, OS was not significant when multivariate analysis was used to control for potential confounding factors. CONCLUSION In our single-institution retrospective review of patients treated with ExRT or ChRT, no significant differences were found in LRC, DMFS, DSS, or OS.


Head and Neck-journal for The Sciences and Specialties of The Head and Neck | 2004

Simplifying head and neck microvascular reconstruction

Eben L. Rosenthal; William R. Carroll; Mathew Dobbs; J. Scott Magnuson; Mark K. Wax; Glenn E. Peters

Free‐tissue transfer has become the preferred method of head and neck reconstruction but is a technique that is considered to use excessive hospital resources.


Laryngoscope | 2003

Expression of Extracellular Matrix Metalloprotease Inducer in Laryngeal Squamous Cell Carcinoma

Eben L. Rosenthal; Satya Shreenivas; Glenn E. Peters; William E. Grizzle; Renee A. Desmond; Candece L. Gladson

Objectives/Hypothesis Head and neck cancer tumor cell invasion is responsible for both local destruction and distant metastasis. Invasion is largely mediated by matrix metalloproteases that are thought to be induced by tumor cell derived extracellular matrix metalloprotease inducer (EMMPRIN) in surrounding fibroblasts. We hypothesize that EMMPRIN is overexpressed in laryngeal cancer.


Laryngoscope | 2013

Outcomes in head and neck reconstruction by surgical site and donor site

John W. Frederick; Larissa Sweeny; William R. Carroll; Glenn E. Peters; Eben L. Rosenthal

Define surgical outcomes of specific donor sites for free tissue transfer in head and neck reconstruction.


Laryngoscope | 2001

Molecular differences in mucoepidermoid carcinoma and adenoid cystic carcinoma of the major salivary glands.

Mark D. Gibbons; Upender Manne; William R. Carroll; Glenn E. Peters; Heidi L. Weiss; William E. Grizzle

Objective/Hypothesis Mucoepidermoid carcinoma (MEC) and adenoid cystic carcinoma (ACC), the most common malignancies of the major salivary glands, are clinically and pathologically different. To determine whether MEC and ACC have different molecular characteristics, we examined the expression of erbB‐2, erbB‐3, epidermal growth factor receptor (EGFR), and transforming growth factor‐α (TGF‐α), important molecular features in other malignancies.


Head and Neck-journal for The Sciences and Specialties of The Head and Neck | 1999

Fatty acid synthase expression is increased in neoplastic lesions of the oral tongue.

Helen Krontiras; G. Dean Roye; Samuel E. Beenken; Russell B. Myers; Matthew S. Mayo; Glenn E. Peters; William E. Grizzle

Fatty acid synthase (FASE) is required for fatty acid synthesis. Elevated levels of FASE have been observed in a variety of malignancies.


American Journal of Clinical Oncology | 1999

Concomitant chemotherapy and reirradiation as management for recurrent cancer of the head and neck.

S.A. Spencer; Richard H. Wheeler; Glenn E. Peters; Samuel W. Beenken; Ruby F. Meredith; Judy L. Smith; Wendy Conner; Merle M. Salter

Thirty-five patients with inoperable recurrent head and neck cancer previously treated with definitive irradiation were treated with reirradiation and concomitant chemotherapy. Patient records were retrospectively reviewed to assess toxicity, response, and survival. Patients received one of three regimens: 1) 40 Gy total (2 Gy daily), 300 mg/m2 5-fluorouracil intravenous bolus, and 2 g hydroxyurea orally daily for 5 days; 2) 48 Gy total (1.2 Gy twice daily), 300 mg/m2 5-fluorouracil intravenous bolus, and 1.5 g hydroxyurea orally daily for 5 days; 3) 60 Gy total (1.5 Gy twice daily), 300 mg/m2 5-fluorouracil intravenous bolus, and 1.5 g hydroxyurea orally daily for 5 days. For all regimens, treatment was given only on weeks 1, 3, 5, and 7. Acute toxicity was mainly hematologic and was less severe with the lower hydroxyurea dose. Acute mucosal and skin toxicity was acceptable for all regimens. Late toxicity was noted in 4 of 17 patients who survived 12 months or more. Late effects were Radiation Therapy Oncology Group grade 3 or less. Fifteen of 35 patients achieved a complete response, and 11 of 35 patients achieved a partial response. The median survival rate was 10.5 months. There was no significant difference in responses or median survival between the groups. Reirradiation of head and neck cancer with 5-fluorouracil and hydroxyurea offers acceptable acute toxicity and minimal late effects. The clinical response rates and median survival are encouraging. Further investigation is warranted.


Head and Neck-journal for The Sciences and Specialties of The Head and Neck | 2003

Phase 1 trial of combined chemotherapy and reirradiation for recurrent unresectable head and neck cancer.

S.A. Spencer; Richard Wheeler; Glenn E. Peters; Ruby F. Meredith; Sam Beenken; Lisle Nabel; Ann Wooten; Seng-jaw Soong; Merle M. Salter

The management of recurrent unresectable head and neck cancer remains a challenging problem. Based on the circadian rhythm concept, we sought to determine the maximum tolerated dose (MTD) of infusional 5‐flourouracil (5‐FU), hydroxyurea (HU), and reirradiation (RT).

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William R. Carroll

University of Alabama at Birmingham

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S.A. Spencer

University of Alabama at Birmingham

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J. Scott Magnuson

University of Alabama at Birmingham

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Ruby F. Meredith

University of Alabama at Birmingham

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Lisle Nabell

University of Alabama at Birmingham

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James A. Bonner

University of Alabama at Birmingham

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Renee A. Desmond

University of Alabama at Birmingham

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William E. Grizzle

University of Alabama at Birmingham

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James R. Boyce

University of Alabama at Birmingham

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