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SEER collects and publishes cancer incidence and survival data from population-based cancer registries covering approximately 34.6% of the population of the United States. SEER coverage includes 30.0% of African Americans, 44% of Hispanics, 49.3% of American Indians and Alaska Natives, 57.5% of Asians, and 68.5% of Hawaiian/Pacific Islanders. [3]
In 2021, NCI undertook a pilot project to oversample cancer survivors using three cancer registries from the Surveillance, Epidemiology, and End Results (SEER) Program (https://seer.cancer.gov) as a sampling frame of cancer survivors. The pilot project, called HINTS-SEER, was designed to provide a larger sample of cancer survivors for analyses.
The National Program of Cancer Registries (NPCR) was established by Congress through the Cancer Registries Amendment Act in 1992, and administered by the Centers for Disease Control and Prevention (CDC). [2] NPCR and SEER together collect cancer data for the entire U.S. population.
One of the largest and most important cancer registries is Surveillance Epidemiology and End Results (SEER), administered by the US Federal government. [ 5 ] Health information privacy concerns have led to the restricted use of cancer registry data in the United States Department of Veterans Affairs [ 6 ] [ 7 ] [ 8 ] and other institutions. [ 9 ]
There are currently over 60,000 clinical trials related to cancer registered on ClinicalTrials.gov, so novel approaches to cancer treatment are continuing to be developed. [18] The NCI lists over 100 targeted therapies that have been approved for the treatment of 26 different cancer types by the United States Food and Drug Administration. [19]
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