Autor: |
Ellis L; Libby Ellis, Alison J. Canchola, and Scarlett Lin Gomez, Cancer Prevention Institute of California, Fremont; Libby Ellis, David Spiegel, and Uri Ladabaum, Stanford Cancer Institute; David Spiegel, Uri Ladabaum, and Robert Haile, Stanford University School of Medicine, Stanford; Robert Haile, Cedars-Sinai Medical Center, Los Angeles; and Scarlett Lin Gomez, University of California, San Francisco, San Francisco, CA., Canchola AJ; Libby Ellis, Alison J. Canchola, and Scarlett Lin Gomez, Cancer Prevention Institute of California, Fremont; Libby Ellis, David Spiegel, and Uri Ladabaum, Stanford Cancer Institute; David Spiegel, Uri Ladabaum, and Robert Haile, Stanford University School of Medicine, Stanford; Robert Haile, Cedars-Sinai Medical Center, Los Angeles; and Scarlett Lin Gomez, University of California, San Francisco, San Francisco, CA., Spiegel D; Libby Ellis, Alison J. Canchola, and Scarlett Lin Gomez, Cancer Prevention Institute of California, Fremont; Libby Ellis, David Spiegel, and Uri Ladabaum, Stanford Cancer Institute; David Spiegel, Uri Ladabaum, and Robert Haile, Stanford University School of Medicine, Stanford; Robert Haile, Cedars-Sinai Medical Center, Los Angeles; and Scarlett Lin Gomez, University of California, San Francisco, San Francisco, CA., Ladabaum U; Libby Ellis, Alison J. Canchola, and Scarlett Lin Gomez, Cancer Prevention Institute of California, Fremont; Libby Ellis, David Spiegel, and Uri Ladabaum, Stanford Cancer Institute; David Spiegel, Uri Ladabaum, and Robert Haile, Stanford University School of Medicine, Stanford; Robert Haile, Cedars-Sinai Medical Center, Los Angeles; and Scarlett Lin Gomez, University of California, San Francisco, San Francisco, CA., Haile R; Libby Ellis, Alison J. Canchola, and Scarlett Lin Gomez, Cancer Prevention Institute of California, Fremont; Libby Ellis, David Spiegel, and Uri Ladabaum, Stanford Cancer Institute; David Spiegel, Uri Ladabaum, and Robert Haile, Stanford University School of Medicine, Stanford; Robert Haile, Cedars-Sinai Medical Center, Los Angeles; and Scarlett Lin Gomez, University of California, San Francisco, San Francisco, CA., Gomez SL; Libby Ellis, Alison J. Canchola, and Scarlett Lin Gomez, Cancer Prevention Institute of California, Fremont; Libby Ellis, David Spiegel, and Uri Ladabaum, Stanford Cancer Institute; David Spiegel, Uri Ladabaum, and Robert Haile, Stanford University School of Medicine, Stanford; Robert Haile, Cedars-Sinai Medical Center, Los Angeles; and Scarlett Lin Gomez, University of California, San Francisco, San Francisco, CA. |
Abstrakt: |
Purpose Racial/ethnic disparities in cancer survival in the United States are well documented, but the underlying causes are not well understood. We quantified the contribution of tumor, treatment, hospital, sociodemographic, and neighborhood factors to racial/ethnic survival disparities in California. Materials and Methods California Cancer Registry data were used to estimate population-based cancer-specific survival for patients diagnosed with breast, prostate, colorectal, or lung cancer between 2000 and 2013 for each racial/ethnic group (non-Hispanic black, Hispanic, Asian American and Pacific Islander, and separately each for Chinese, Japanese, and Filipino) compared with non-Hispanic whites. The percentage contribution of factors to overall racial/ethnic survival disparities was estimated from a sequence of multivariable Cox proportional hazards models. Results In baseline models, black patients had the lowest survival for all cancer sites, and Asian American and Pacific Islander patients had the highest, compared with whites. Mediation analyses suggested that stage at diagnosis had the greatest influence on overall racial/ethnic survival disparities accounting for 24% of disparities in breast cancer, 24% in prostate cancer, and 16% to 30% in colorectal cancer. Neighborhood socioeconomic status was an important factor in all cancers, but only for black and Hispanic patients. The influence of marital status on racial/ethnic disparities was stronger in men than in women. Adjustment for all covariables explained approximately half of the overall survival disparities in breast, prostate, and colorectal cancer, but it explained only 15% to 40% of disparities in lung cancer. Conclusion Overall reductions in racial/ethnic survival disparities were driven largely by reductions for black compared with white patients. Stage at diagnosis had the largest effect on racial/ethnic survival disparities, but earlier detection would not entirely eliminate them. The influences of neighborhood socioeconomic status and marital status suggest that social determinants, support mechanisms, and access to health care are important contributing factors. |