Mary Jo Lund
Emory University
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Featured researches published by Mary Jo Lund.
Cancer | 2004
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
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
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)
Journal of Clinical Oncology | 2012
Xiao-Cheng Wu; Mary Jo Lund; Gretchen Kimmick; Lisa C. Richardson; Susan A. Sabatino; Vivien W. Chen; Steven T. Fleming; Cyllene R. Morris; Bin Huang; Amy Trentham-Dietz; Joseph Lipscomb
PURPOSE For breast cancer, guidelines direct the delivery of adjuvant systemic therapy on the basis of lymph node status, histology, tumor size, grade, and hormonal receptor status. We explored how race/ethnicity, insurance, census tract-level poverty and education, and hospital Commission on Cancer (CoC) status were associated with the receipt of guideline-concordant adjuvant systemic therapy. METHODS Locoregional breast cancers diagnosed in 2004 (n = 6,734) were from the National Program of Cancer Registries-funded seven-state Patterns of Care study of the Centers for Disease Control and Prevention. Predictors of guideline-concordant (receiving/not receiving) adjuvant systemic therapy, according to National Comprehensive Cancer Network Guidelines, were explored by logistic regression. RESULTS Overall, 35% of women received nonguideline chemotherapy, 12% received nonguideline regimens, and 20% received nonguideline hormonal therapy. Significant predictors of nonguideline chemotherapy included Medicaid insurance (odds ratio [OR], 0.66; 95% CI, 0.50 to 0.86), high-poverty areas (OR, 0.77; 95% CI, 0.62 to 0.96), and treatment at non-CoC hospitals (OR, 0.69; 95% CI, 0.56 to 0.85), with adjustment for age, registry, and clinical variables. Predictors of nonguideline regimens among chemotherapy recipients included lack of insurance (OR, 0.47; 95% CI, 0.25 to 0.92), high-poverty areas (OR, 0.71; 95% CI, 0.51 to 0.97), and low-education areas (OR, 0.65; 95% CI, 0.48 to 0.89) after adjustment. Living in high-poverty areas (OR, 0.78; 95% CI, 0.64 to 0.96) and treatment at non-CoC hospitals (OR, 0.68; 95% CI, 0.55 to 0.83) predicted nonguideline hormonal therapy after adjustment. ORs for poverty, education, and insurance were attenuated in the full models. CONCLUSION Sociodemographic and hospital factors are associated with guideline-concordant use of systemic therapy for breast cancer. The identification of modifiable factors that lead to nonguideline treatment may reduce disparities in breast cancer survival.
Cancer | 2006
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 | 2010
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.
Cancer | 2008
Mary Jo Lund; Eboneé N. Butler; Harvey L. Bumpers; Joel Okoli; Monica Rizzo; Nadjo Hatchett; Victoria L. Green; Otis W. Brawley; Gabriela Oprea-Ilies; Sheryl Gabram
A disparate proportion of breast cancer deaths occur among young women, those of African‐American (AA) ancestry, and particularly young AA women. Estrogen receptors (ER), progesterone receptors (PR), and human epidermal growth factor receptor‐2 (HER‐2) are key clinically informative biomarkers. The triple‐negative (ER‐/PR‐/HER‐2‐) tumor subgroup is intrinsically resistant to treatment and portends a poor prognosis. Age, race, and socioeconomic status have been associated with triple‐negative tumors (TNT). In the current study, the authors investigated breast cancer subgroups among patients in an urban cancer center serving a multiracial, low socioeconomic population.
Cancer | 2008
Sheryl Gabram; Mary Jo Lund; Jessica Gardner; Nadjo Hatchett; Harvey L. Bumpers; Joel Okoli; Monica Rizzo; Barbara Johnson; Gina B. Kirkpatrick; Otis W. Brawley
Compared with white women, African‐American (AA) women who are diagnosed with breast cancer experience an excess in mortality. To improve outcomes, the authors implemented community education and outreach initiatives in their cancer center, at affiliated primary care sites, and in the surrounding communities. They then assessed the effectiveness of these outreach initiatives and internal patient navigation on stage of diagnosis.
Cancer | 2012
Mary Jo Lund; Marina Mosunjac; Kelly M. Davis; Sheryl Gabram-Mendola; Monica Rizzo; Harvey L. Bumpers; Sherita Hearn; Amelia Zelnak; Toncred M. Styblo; Ruth O'Regan
African American (AA) women experience higher breast cancer mortality than white (W) women. These differences persist even among estrogen receptor (ER)‐positive breast cancers. The 21‐gene recurrence score (RS) predicts recurrence in patients with ER‐positive/lymph node‐negative breast cancer according to RS score—low risk (RS, 0‐18), intermediate risk (RS, 19‐31), and high risk (RS, >31). The high‐risk group is most likely to benefit from chemotherapy, to achieve minimal benefit from hormonal therapy, and to exhibit lower ER levels (intrinsically luminal B cancers). In the current study, the authors investigated racial differences in RS testing, scores, treatment, and outcome.
Cancer | 2009
Monica Rizzo; Mary Jo Lund; Marina Mosunjac; Harvey L. Bumpers; Leslie Holmes; Ruth O'Regan; Otis W. Brawley; Sheryl Gabram
Stage III breast cancers account for about 6% to 7% of all invasive breast cancers diagnosed annually in the United States. In African American (AA) women, the incidence of stage III breast cancers is almost double that in Caucasian women. The aim of this study was to correlate age, receptor status, nuclear grade, and differences in treatment modalities for stage III breast cancer in an inner‐city hospital serving a large AA population.