The history and use of cancer registry data by public health cancer control programs in the United States

Because cancer registry data provide a census of cancer cases, registry data can be used to: 1) define and monitor cancer incidence at the local, state, and national levels; 2) investigate patterns of cancer treatment; and 3) evaluate the effectiveness of public health efforts to prevent cancer case...

Full description

Saved in:
Bibliographic Details
Published in:Cancer Vol. 123; no. S24; pp. 4969 - 4976
Main Authors: White, Mary C., Babcock, Frances, Hayes, Nikki S., Mariotto, Angela B., Wong, Faye L., Kohler, Betsy A., Weir, Hannah K.
Format: Journal Article
Language:English
Published: United States Wiley Subscription Services, Inc 15-12-2017
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Because cancer registry data provide a census of cancer cases, registry data can be used to: 1) define and monitor cancer incidence at the local, state, and national levels; 2) investigate patterns of cancer treatment; and 3) evaluate the effectiveness of public health efforts to prevent cancer cases and improve cancer survival. The purpose of this article is to provide a broad overview of the history of cancer surveillance programs in the United States, and illustrate the expanding ways in which cancer surveillance data are being made available and contributing to cancer control programs. The article describes the building of the cancer registry infrastructure and the successful coordination of efforts among the 2 federal agencies that support cancer registry programs, the Centers for Disease Control and Prevention and the National Cancer Institute, and the North American Association of Central Cancer Registries. The major US cancer control programs also are described, including the National Comprehensive Cancer Control Program, the National Breast and Cervical Cancer Early Detection Program, and the Colorectal Cancer Control Program. This overview illustrates how cancer registry data can inform public health actions to reduce disparities in cancer outcomes and may be instructional for a variety of cancer control professionals in the United States and in other countries. Cancer 2017;123:4969‐76. Published 2017. This article is a U.S. Government work and is in the public domain in the USA. This article provides a broad overview of the history of cancer surveillance programs in the United States and the use of cancer registry data for cancer control programs at the Centers for Disease Control and Prevention. The information in this overview illustrates the ways in which cancer surveillance data can be used to define and monitor burden at the local, state, and national levels and evaluate the effectiveness of public health efforts for cancer control and improved cancer survival.
Bibliography:The findings and conclusions in this report are those of the authors and do not necessarily reflect the official position of the CDC.
We thank Nicholas (Tony) Pearson‐Clarke for editorial service and Keely Beck for assistance with compiling cited references.
has been sponsored by the U.S. Centers for Disease Control and Prevention (CDC), an Agency of the Department of Health and Human Services.
The CONCORD‐2 study was approved by the Ethics and Confidentiality Committee of the UK's statutory National Information Governance Board (now the Health Research Authority) (ref ECC 3‐04(i)/2011) and by the National Health Service Research Ethics Service (Southeast; 11/LO/0331).
This Supplement edition of
Cancer
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0008-543X
1097-0142
DOI:10.1002/cncr.30905