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Evaluation of North American Association of Central Cancer Registries' (NAACCR) Data for Use in Population-Based Cancer Survival Studies
Author(s) -
Hannah K. Weir,
C. J. Johnson,
Angela B. Mariotto,
Donna Turner,
R. J. Wilson,
Diane Nishri,
Kevin C. Ward
Publication year - 2014
Publication title -
jnci monographs
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.014
H-Index - 85
eISSN - 1745-6614
pISSN - 1052-6773
DOI - 10.1093/jncimonographs/lgu018
Subject(s) - medicine , epidemiology , cancer , demography , surveillance, epidemiology, and end results , population , cancer registry , cause of death , relative survival , environmental health , disease , sociology
Follow-up procedures vary among cancer registries in North America. US registries are funded by the Surveillance, Epidemiology, and End Results (SEER) Program and/or the National Program of Cancer Registries (NPCR). SEER registries ascertain vital status and date of last contact to meet follow-up standards. NPCR and Canadian registries primarily conduct linkages with local and national death records to ascertain deaths. Data on patients diagnosed between 2002 through 2006 and followed through 2007 were obtained from 51 registries. Registries that met follow-up standards or, at a minimum, conducted linkages with local and national death records had comparable age-standardized five-year survival estimates (all sites and races combined): 63.9% SEER, 63.1% NPCR, and 62.6% Canada. Estimates varied by cancer site. Survival data from registries using different follow-up procedures are comparable if death ascertainment is complete and all nondeceased patients are presumed to be alive to the end of the study period.

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