Women with African ancestry in western, sub-Saharan Africa and in the United States represent a population subset facing an increased risk of being diagnosed with biologically aggressive phenotypes of breast cancer that are negative for the estrogen receptor, the progesterone receptor, and the HER2/neu marker. These tumors are commonly referred to as triple-negative breast cancer. Disparities in breast cancer incidence and outcome related to racial or ethnic identity motivated the establishment of the International Breast Registry, on the basis of partnerships between the Komfo Anokye Teaching Hospital in Kumasi, Ghana, the University of Michigan Comprehensive Cancer Center in Ann Arbor, Michigan, and the Henry Ford Health System in Detroit, Michigan. This research collaborative has featured educational training programs as well as scientific investigations related to the comparative biology of breast cancer in Ghanaian African, African American, and white/European American patients. Currently, the International Breast Registry has expanded to include African American patients throughout the United States by partnering with the Sisters Network (a national African American breast cancer survivors’ organization) and additional sites in Ghana (representing West Africa) as well as Ethiopia (representing East Africa). Its activities are now coordinated through the Henry Ford Health System International Center for the Study of Breast Cancer Subtypes. Herein, we review the history and results of this international program at its 10-year anniversary.
Original ArticleAbstract Purpose: The aim of this study was to evaluate dosimetric differences between pencil beam convolution (PBC) algorithm and anisotropic analytical algorithm (AAA) calculations in patients with lung and esophageal cancers. Methods: The existing plans calculated with PBC for 60 patients treated in 2012 were recalculated with AAA maintaining the same beam geometry and dose monitor units. For these plans, dose prescription ranges were 41.4 Gy to 56.0 Gy for esophageal cancers and 50.0 Gy to 64.0 Gy for lung cancers. Dosimetric variables were the 95% PTV coverage, mean PTV dose, maximum spinal cord dose, lung V5Gy, and lung V20Gy. Results: The 95% PTV coverage's for both lung and esophageal tumors were reduced when recalculated with AAA. Maximum spinal cord doses for lung cancer patients were reduced by 0.7 Gy and by 0.3 Gy for esophageal cancer patients on AAA. On the other hand, lung V5Gy had 3.5% increase for both lung and esophageal cancer patients on AAA, whereas lung V20Gy increased by 1.5% also on AAA for esophageal cancer patients. Conclusion: These clinical results confirm the differences between AAA and PBC algorithms as observed in phantom dosimetric studies, and give an indication of the clinical implications of changing from one calculation algorithm to another.
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