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Multicenter Study
. 2012 Dec;47(12):1308-22.
doi: 10.1007/s00535-012-0603-2. Epub 2012 May 25.

Age at diagnosis of inflammatory bowel disease influences early development of colorectal cancer in inflammatory bowel disease patients: a nationwide, long-term survey

Affiliations
Multicenter Study

Age at diagnosis of inflammatory bowel disease influences early development of colorectal cancer in inflammatory bowel disease patients: a nationwide, long-term survey

J E Baars et al. J Gastroenterol. 2012 Dec.

Abstract

Background: Data on clinical characteristics of patients with inflammatory bowel disease (IBD)-related colorectal cancer (CRC) are scarce and mainly originate from tertiary referral centres. We studied patient and disease characteristics of IBD-related CRC in a nationwide IBD cohort in general hospitals. Main outcome parameters were time to develop CRC, and factors associated with early CRC development.

Methods: All IBD patients diagnosed with CRC between 1 January 1990 and 1 July 2006 were identified using a nationwide automated pathology database (PALGA). Patient charts were assessed to confirm diagnosis and collect clinical data. Early CRC was defined as CRC diagnosed less than 8 years after IBD diagnosis. Statistical analysis was performed using descriptive statistics, independent t tests, binary logistic regression and Cox-regression analysis.

Results: Diagnosis of IBD-related CRC was confirmed in 251 patients (171 ulcerative colitis, 77 Crohn's disease, 3 unclassified colitis), 161 males (64 %). Median time from IBD diagnosis to CRC diagnosis was 12 years (IQR 4-20); 89 patients (35 %) developed early CRC. Type of IBD, gender, concomitant PSC, pseudopolyps, extent of inflammation, and medication use were not related to early CRC (p > 0.05). IBD diagnosis at older age (HR for 10 years older age 2.25; 95 % CI 1.92-2.63) was related to early CRC. Twenty-three patients (12 %) had been included in a surveillance programme prior to CRC diagnosis. Patients in the surveillance group had a significantly better tumor stage (p = 0.004).

Conclusions: We emphasize the problem of a high proportion of IBD-associated CRCs developing before the recommended start of surveillance. Therefore, we suggest that older age at IBD onset could be an additional factor to start surveillance in IBD patients.

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Figures

Fig. 1
Fig. 1
Flow chart study population
Fig. 2
Fig. 2
Age at IBD diagnosis versus age at CRC diagnosis. The age at IBD diagnosis is plotted against the age at which patients are diagnosed with CRC. This figure demonstrates that age at onset of IBD is not related to the age at which patients develop CRC
Fig. 3
Fig. 3
Age at CRC diagnosis is independent of duration of IBD. The duration of IBD is plotted against the median age at which patients developed CRC. This figure demonstrates that age at CRC-diagnosis is independent of duration of IBD
Fig. 4
Fig. 4
Age at IBD diagnosis is related to the time to develop CRC. This figure shows the time to develop CRC against the age at which patients were diagnosed with IBD. This shows that age at IBD diagnosis is related to the time to develop CRC

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