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PMID: 24047059 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Long-term colorectal-cancer incidence and mortality after lower endoscopy.

The New England journal of medicine ·Vol. 369 ·No. 12 ·2013-09-19 ·Pages 1095-105

Nishihara R, Wu K, Lochhead P, Morikawa T, Liao X, Qian ZR, Inamura K, Kim SA, Kuchiba A, Yamauchi M, Imamura Y, Willett WC, Rosner BA, Fuchs CS, Giovannucci E, Ogino S, Chan AT

Abstract

Colonoscopy and sigmoidoscopy provide protection against colorectal cancer, but the magnitude and duration of protection, particularly against cancer of the proximal colon, remain uncertain. We examined the association of the use of lower endoscopy (updated biennially from 1988 through 2008) with colorectal-cancer incidence (through June 2010) and colorectal-cancer mortality (through June 2012) among participants in the Nurses' Health Study and the Health Professionals Follow-up Study. Among 88,902 participants followed over a period of 22 years, we documented 1815 incident colorectal cancers and 474 deaths from colorectal cancer. With endoscopy as compared with no endoscopy, multivariate hazard ratios for colorectal cancer were 0.57 (95% confidence interval [CI], 0.45 to 0.72) after polypectomy, 0.60 (95% CI, 0.53 to 0.68) after negative sigmoidoscopy, and 0.44 (95% CI, 0.38 to 0.52) after negative colonoscopy. Negative colonoscopy was associated with a reduced incidence of proximal colon cancer (multivariate hazard ratio, 0.73; 95% CI, 0.57 to 0.92). Multivariate hazard ratios for death from colorectal cancer were 0.59 (95% CI, 0.45 to 0.76) after screening sigmoidoscopy and 0.32 (95% CI, 0.24 to 0.45) after screening colonoscopy. Reduced mortality from proximal colon cancer was observed after screening colonoscopy (multivariate hazard ratio, 0.47; 95% CI, 0.29 to 0.76) but not after sigmoidoscopy. As compared with colorectal cancers diagnosed in patients more than 5 years after colonoscopy or without any prior endoscopy, those diagnosed in patients within 5 years after colonoscopy were more likely to be characterized by the CpG island methylator phenotype (CIMP) (multivariate odds ratio, 2.19; 95% CI, 1.14 to 4.21) and microsatellite instability (multivariate odds ratio, 2.10; 95% CI, 1.10 to 4.02). Colonoscopy and sigmoidoscopy were associated with a reduced incidence of cancer of the distal colorectum; colonoscopy was also associated with a modest reduction in the incidence of proximal colon cancer. Screening colonoscopy and sigmoidoscopy were associated with reduced colorectal-cancer mortality; only colonoscopy was associated with reduced mortality from proximal colon cancer. Colorectal cancer diagnosed within 5 years after colonoscopy was more likely than cancer diagnosed after that period or without prior endoscopy to have CIMP and microsatellite instability. (Funded by the National Institutes of Health and others.).

MeSH Terms
Adenoma/diagnosis,epidemiology,mortality,prevention & control Aged Cohort Studies Colonic Polyps/genetics,pathology Colonoscopy Colorectal Neoplasms/diagnosis,epidemiology,mortality,prevention & control DNA, Neoplasm/analysis Early Detection of Cancer Female Humans Incidence Male Microsatellite Instability Middle Aged Multivariate Analysis Mutation Sigmoidoscopy United States/epidemiology
Chemicals
DNA, Neoplasm
Authors & Affiliations
17 authors, click to expand affiliations / ORCID
Nishihara Reiko
Department of Medical Oncology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, MA, USA.
Wu Kana
Lochhead Paul
Morikawa Teppei
Liao Xiaoyun
Qian Zhi Rong
Inamura Kentaro
Kim Sun A
Kuchiba Aya
Yamauchi Mai
Imamura Yu
Willett Walter C
Rosner Bernard A
Fuchs Charles S
Giovannucci Edward
Ogino Shuji
Chan Andrew T
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Article Info
Journal
The New England journal of medicine
Abbr.
N Engl J Med
ISSN
1533-4406
Published
2013-09-19
Pages
1095-105
Language
English
Region
United States
NLM ID
0255562
PMCID
PMC3840160
Subset
IM
Grants
NCI NIH HHS · P01 CA087969 · United States
NIDDK NIH HHS · P30 DK043351 · United States
NCI NIH HHS · R01 CA137178 · United States
NCI NIH HHS · P01 CA87969 · United States
NCI NIH HHS · P01 CA55075 · United States
NCI NIH HHS · UM1 CA167552 · United States
NCI NIH HHS · P50 CA127003 · United States
Chief Scientist Office · CAF/10/15 · United Kingdom
NCI NIH HHS · P01 CA055075 · United States
NCI NIH HHS · R01 CA151993 · United States
NCI NIH HHS · 1UM1 CA167552 · United States
NIDDK NIH HHS · K24 DK098311 · United States
Corrections
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