A pooled analysis of advanced colorectal neoplasia diagnoses after colonoscopic polypectomy.
A pooled analysis of advanced colorectal neoplasia diagnoses after colonoscopic polypectomy.
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DOI:
10.1053/j.gastro.2008.12.007
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发表时间:
2009-03
期刊:
影响因子:
29.4
通讯作者:
Greenberg ER
中科院分区:
文献类型:
--
作者:
Martínez ME;Baron JA;Lieberman DA;Schatzkin A;Lanza E;Winawer SJ;Zauber AG;Jiang R;Ahnen DJ;Bond JH;Church TR;Robertson DJ;Smith-Warner SA;Jacobs ET;Alberts DS;Greenberg ER
Limited data exist regarding the actual risk of developing advanced adenomas and cancer following polypectomy or the factors that determine risk. We pooled individual data from 8 prospective studies comprising 9167 men and women aged 22 to 80 with previously-resected colorectal adenomas to quantify their risk of developing subsequent advanced adenoma or cancer as well as identify factors associated with development of advanced colorectal neoplasms during surveillance. During a median follow-up of 47.2 months, advanced colorectal neoplasia was diagnosed in 1082 (11.8%) of the patients, 58 of whom (0.6%) had invasive cancer. Risk of a metachronous advanced adenoma was higher among patients with 5 or more baseline adenomas (24.1%; SE=2.2) and those with an adenoma 20 mm in size or greater (19.3%; SE=1.5). Risk factor patterns were similar for advanced adenomas and invasive cancer. In multivariate analyses, older age (P <0.0001 for trend) and male sex (odds ratio [OR], 1.40; 95% confidence interval [CI] 1.19–1.65) were significantly associated with increased risk of metachronous advanced neoplasia, as were the number and size of prior adenomas (P <0.0001 for trend), the presence of villous features (OR, 1.28; 95% CI 1.07–1.52), and proximal location (OR, 1.68; 95% CI 1.43–1.98). High-grade dysplasia was not independently associated with metachronous advanced neoplasia after adjustment for other adenoma characteristics. Occurrence of advanced colorectal neoplasia is common following polypectomy. Factors that are most strongly associated with risk of advanced neoplasia are patient age and the number and size of prior adenomas.
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影响因子:
158.5
作者:
Bertagnolli, Monica M.;Eagle, Craig J.;Hawk, Ernest T.
通讯作者:
Hawk, Ernest T.
影响因子:
8.4
作者:
Butterworth, AS;Higgins, JPT;Pharoah, P
通讯作者:
Pharoah, P
影响因子:
158.5
作者:
ATKIN, WS;MORSON, BC;CUZICK, J
通讯作者:
CUZICK, J
影响因子:
6.4
作者:
Bertario, L;Russo, A;Spinelli, P
通讯作者:
Spinelli, P
DOI:
10.1016/0197-2456(86)90046-2
发表时间:
1986-09-01
期刊:
CONTROLLED CLINICAL TRIALS
影响因子:
--
作者:
DERSIMONIAN, R;LAIRD, N
通讯作者:
LAIRD, N