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Dive into the research topics where J. William Eley is active.

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Featured researches published by J. William Eley.


Journal of Clinical Oncology | 2001

Quality-of-life outcomes after primary androgen deprivation therapy: results from the prostate cancer outcomes study

Arnold L. Potosky; Kevin B. Knopf; Limin X. Clegg; Peter C. Albertsen; Janet L. Stanford; Ann S. Hamilton; Frank D. Gilliland; J. William Eley; Robert A. Stephenson; Richard M. Hoffman

PURPOSE To compare health-related quality-of-life outcomes after primary androgen deprivation (AD) therapy with orchiectomy versus luteinizing hormone-releasing hormone (LHRH) agonists for patients with prostate cancer. PATIENTS AND METHODS Men (n = 431) newly diagnosed with all stages of prostate cancer from six geographic regions who participated in the Prostate Cancer Outcomes Study and who received primary AD therapy but no other treatments within 12 months of initial diagnosis were included in a study of health outcomes. Comparisons were statistically adjusted for patient sociodemographic and clinical characteristics, timing of therapy, and use of combined androgen blockade. RESULTS More than half of the patients receiving primary AD therapy had been initially diagnosed with clinically localized prostate cancer. Among these patients, almost two thirds were at high risk of progression on the basis of prognostic factors. Sexual function outcomes were similar by treatment group both before and after implementation of AD therapy. LHRH patients reported more breast swelling than did orchiectomy patients (24.9% v 9.7%, P <.01). LHRH patients reported more physical discomfort and worry because of cancer or its treatment than did orchiectomy patients. LHRH patients assessed their overall health as fair or poor more frequently than did orchiectomy patients (35.4% v 28.1%, P =.01) and also were less likely to consider themselves free of prostate cancer after treatment. CONCLUSION Most endocrine-related health outcomes are similar after surgical versus medical primary hormonal therapy. Stage at diagnosis had little effect on outcomes. These results provide representative information comparing surgical and medical AD therapy that may be used by physicians and patients to inform treatment decisions.


Cancer | 2004

Racial differences in diagnosis, treatment, and clinical delays in a population-based study of patients with newly diagnosed breast carcinoma†‡

Karin Gwyn; Melissa L. Bondy; Deborah S. Cohen; Mary Jo Lund; Jonathan M. Liff; Elaine W. Flagg; Louise A. Brinton; J. William Eley; Ralph J. Coates

Few studies have addressed the issue of whether delays in the interval between medical consultation and the diagnosis and treatment of breast carcinoma are greater for African American women than for white women. The authors examined differences with respect to these delays and analyzed the factors that may have contributed to such differences among women ages 20–54 years who had invasive breast carcinoma diagnosed between 1990 and 1992 and who lived in Atlanta, Georgia.


Cancer | 2004

Racial differences in the expression of cell cycle-regulatory proteins in breast carcinoma: Study of young African American and white women in Atlanta, Georgia

Peggy L. Porter; Mary Jo Lund; Ming Gang Lin; Xiaopu Yuan; Jonathan M. Liff; Elaine W. Flagg; Ralph J. Coates; J. William Eley

African‐American (AA) women are more likely to be diagnosed with an advanced stage of breast carcinoma than are white women. After adjustment for disease stage, many studies indicate that tumors in AA women are more likely than tumors in white women are to exhibit a high level of cell proliferation and features of poor prognosis. The purpose of the current study was to compare tumor characteristics and cell cycle alterations in AA women and white women that might affect the aggressiveness of breast carcinoma.


Cancer Epidemiology, Biomarkers & Prevention | 2006

General and Abdominal Obesity and Survival among Young Women with Breast Cancer

Page E. Abrahamson; Marilie D. Gammon; Mary Jo Lund; Elaine W. Flagg; Peggy L. Porter; June Stevens; Christine A. Swanson; Louise A. Brinton; J. William Eley; Ralph J. Coates

Among postmenopausal women, obesity is linked to increased risk of breast cancer and poorer subsequent survival. For premenopausal women, obesity may reduce incidence, but less is known about its effect on prognosis, particularly for abdominal obesity. This study investigated whether general or abdominal obesity at diagnosis influenced survival in a cohort of young women with breast cancer. A population-based follow-up study was conducted among 1,254 women ages 20 to 54 who were diagnosed with invasive breast cancer between 1990 and 1992 in Atlanta or New Jersey. Women were interviewed within several months of diagnosis and asked about their weight and height at age 20 and in the year before diagnosis. Study personnel did anthropometric measures at the interview. With 8 to 10 years of follow-up, all-cause mortality status was determined using the National Death Index (n = 290 deaths). Increased mortality was observed for women who were obese [body mass index (BMI), ≥30] at the time of interview compared with women of ideal weight [BMI, 18.5-24.9; stage- and income-adjusted hazard ratio (HR), 1.48; 95% confidence interval (95% CI), 1.09-2.01]. A similar result was seen for the highest versus lowest quartile of waist-to-hip ratio (HR, 1.52; 95% CI, 1.05-2.19). Strong associations with mortality were found for women who were obese at age 20 (HR, 2.49; 95% CI, 1.15-5.37) or who were overweight/obese (BMI, ≥25) at both age 20 and the time of interview (HR, 2.22; 95% CI, 1.45-3.40). This study provides evidence that breast cancer survival is reduced among younger women with general or abdominal obesity. (Cancer Epidemiol Biomarkers Prev 2006;15(10):1871–7)


Cancer | 2006

Recreational physical activity and survival among young women with breast cancer.

Page E. Abrahamson; Marilie D. Gammon; Mary Jo Lund; Julie A. Britton; Stephen W. Marshall; Elaine W. Flagg; Peggy L. Porter; Louise A. Brinton; J. William Eley; Ralph J. Coates

Most epidemiologic studies report a reduced risk of developing breast cancer associated with higher levels of recreational physical activity, but little is known regarding its effect on prognosis.


Cancer | 1992

Treatment plans for black and white women with stage II node‐positive breast cancer: The national cancer institute black/white cancer survival study experience

Hyman B. Muss; Carrie P. Hunter; Margaret N. Wesley; Pelayo Correa; Vivien W. Chen; Raymond S. Greenberg; J. William Eley; Donald F. Austin; Robert J. Kurman; Brenda K. Edwards

Background. The National Cancer Institute Black/White Cancer Survival Study began patient accrual in 1985 and was designed to investigate factors that might contribute to the observed racial differences in survival for cancer of the breast, uterine corpus, colon, and bladder.


Cancer | 2010

Age/race differences in HER2 testing and in incidence rates for breast cancer triple subtypes: a population-based study and first report.

Mary Jo Lund; Eboneé N. Butler; Brionna Y. Hair; Kevin C. Ward; Judy H. Andrews; Gabriella Oprea-Ilies; A. Rana Bayakly; Ruth O'Regan; Paula M. Vertino; J. William Eley

Although US year 2000 guidelines recommended characterizing breast cancers by human epidermal growth factor receptor 2 (HER2), national cancer registries do not collect HER2, rendering a population‐based understanding of HER2 and clinical “triple subtypes” (estrogen receptor [ER] / progesterone receptor [PR] / HER2) largely unknown. We document the population‐based prevalence of HER2 testing / status, triple subtypes and present the first report of subtype incidence rates.


The Journal of Urology | 1999

Predicting extracapsular extension of prostate cancer in men treated with radical prostatectomy: results from the population based prostate cancer outcomes study.

Frank D. Gilliland; Richard M. Hoffman; Ann S. Hamilton; Peter C. Albertsen; J. William Eley; Lynne Harlan; Janet L. Stanford; William C. Hunt; Arnold L. Potosky

PURPOSE We investigated whether clinical information routinely available in community practice could predict extracapsular extension of clinically localized prostate cancer in men undergoing radical prostatectomy. MATERIALS AND METHODS We examined prostate cancer outcomes in a population based sample of 3,826 patients with primary prostate cancer in 6 regions of the United States covered by the Surveillance, Epidemiology, and End Results program. Stratified and weighted logistic regression was used to identify predictors of and probabilities for extracapsular extension of clinically localized tumors treated with radical prostatectomy. RESULTS Nearly 47% of men undergoing radical prostatectomy had extraprostatic extension. The strongest predictors were elevated prostate specific antigen (PSA) greater than 20 versus less than 4 ng./ml. (odds ratio 5.88, 95% confidence interval 2.90 to 11.15), Gleason score greater than 8 versus less than 6 (1.73, 1.04 to 2.87) and age greater than 70 versus less than 50 years (1.91, 0.98 to 3.70). Ethnicity and region were not associated with increased risk of extraprostatic extension. A nomogram developed from our model predicts extracapsular extension ranging from 24% in men younger than 50 years with PSA less than 4 ng./ml. and a Gleason score of less than 7 to 85% in those 70 years old or older with PSA greater than 20 ng./ml. and a Gleason score of 8 or more. If prostatectomy were limited to patients with less than 60% probability of extraprostatic extension based on the nomogram, 95% of those with organ confined cancers would undergo definitive surgery and 18% of those with extracapsular extension would be spared the morbidity of surgery. CONCLUSIONS In a population based analysis of prostate cancer practice patterns PSA, Gleason score and age are clinically useful predictors of extracapsular extension. Although extracapsular extension may be an imperfect predictor of cancer outcomes, our nomogram provides more realistic probabilities for extracapsular extension than those based on institutional series.


Nutrition and Cancer | 1994

Dietary Glutathione Intake in Humans and the Relationship Between Intake and Plasma Total Glutathione Level

Elaine W. Flagg; Ralph J. Coates; J. William Eley; Dean P. Jones; Elaine W. Gunter; Tim Byers; Gladys Block; Raymond S. Greenberg

Glutathione may function as an anticarcinogen by acting as an antioxidant or by binding with cellular mutagens. Orally administered glutathione increases plasma glutathione levels, and plasma glutathione is also synthesized in the liver. To investigate the associations between glutathione intake and plasma glutathione level, we compared dietary intake estimates from food frequency questionnaire data and measured concentrations of plasma total glutathione and other serum antioxidants in 69 white men and women. Daily glutathione intake ranged from 13.0 to 109.9 mg (mean 34.8 mg). Fruits and vegetables were found to contribute over 50% of usual dietary glutathione intake, whereas meats contributed less than 25%. Small negative correlations were observed between dietary and plasma glutathione and, although they were usually not statistically significant, they were generally consistent by different time periods of dietary intake assessment. Adjustment for sex, age, caloric intake, and dietary intake of the sulfur-containing amino acids methionine and cystine did not alter the observed associations. The correlations appeared to be modified, however, by serum vitamin C concentration, with little or no association between dietary and plasma glutathione among those with lower levels of serum vitamin C and stronger negative correlations among those with higher serum vitamin C levels. These findings indicate that factors regulating plasma glutathione concentration are complex and not simply related to dietary glutathione intake or supply of precursor amino acids.


American Journal of Obstetrics and Gynecology | 1995

Endometrial cancer: Stage at diagnosis and associated factors in black and white patients

Rolland J. Barrett; Linda C. Harlan; Margaret N. Wesley; Holly A. Hill; Vivien W. Chen; Linda A. Clayton; Herbert L. Kotz; J. William Eley; Stanley J. Robboy; Brenda K. Edwards

OBJECTIVE This study examined the relationship of clinicopathologic, health status, medical system, and socioeconomic factors to differences in stage at diagnosis of endometrial cancer in black and white patients. STUDY DESIGN A population-based study of 130 black and 329 white patients with invasive endometrial cancer was conducted as part of the National Cancer Institutes Black/White Cancer Survival Study. Logistic regression was used to determine the relative importance of factors thought to be related to stage at diagnosis after age and geographic location were adjusted for. RESULTS High-grade (poorly differentiated) lesions increased the risk for stage III or IV disease (odds ratio 8.3, 95% confidence interval 3.4 to 20.3), as did serous histologic subtype (odds ratio 3.5, 95% confidence interval 1.4 to 8.8) and no usual source of care (odds ratio 5.5, 95% confidence interval 1.4 to 20.9). In the final statistical model these three factors also accounted for the majority of the excess risk of advanced stage for blacks. CONCLUSIONS Black-white racial disparities in stage at diagnosis appear to be related to higher-grade lesions and more aggressive histologic subtypes occurring more frequently in black patients with endometrial cancer.

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Ralph J. Coates

Centers for Disease Control and Prevention

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Elaine W. Flagg

Centers for Disease Control and Prevention

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Peggy L. Porter

Fred Hutchinson Cancer Research Center

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Frank D. Gilliland

University of Southern California

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Raymond S. Greenberg

University of Texas MD Anderson Cancer Center

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Janet L. Stanford

Fred Hutchinson Cancer Research Center

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