Collect data on black and white patients with cancers of the female breast, colon, corpus, or urinary bladder. Specifically: collect patient data; review all phases of the study and make suggestions to make the study more scientifically sound; obtain required local clearances; identify after diagnosis all black cancer patients and matching white cancer patients pertinent to this study; obtain diagnostic slides; obtain permission to contact study patients; obtain informed consent; interview patients; abstract medical records; document progress of the study; maintain completed questionnaires for transfer to Data Coordinating Center, etc.; help interpret data after analysis by NCI; and report progress to NCI.
Prout Jr, George R; Wesley, Margaret N; McCarron, Peter G et al. (2004) Survival experience of black patients and white patients with bladder carcinoma. Cancer 100:621-30 |
Reynolds, P; Hurley, S; Torres, M et al. (2000) Use of coping strategies and breast cancer survival: results from the Black/White Cancer Survival Study. Am J Epidemiol 152:940-9 |
Chen, V W; Fenoglio-Preiser, C M; Wu, X C et al. (1997) Aggressiveness of colon carcinoma in blacks and whites. National Cancer Institute Black/White Cancer Survival Study Group. Cancer Epidemiol Biomarkers Prev 6:1087-93 |
Chen, V W; Correa, P; Kurman, R J et al. (1994) Histological characteristics of breast carcinoma in blacks and whites. Cancer Epidemiol Biomarkers Prev 3:127-35 |
Harlan, L C; Coates, R J; Block, G et al. (1993) Estrogen receptor status and dietary intakes in breast cancer patients. Epidemiology 4:25-31 |