Risk Factors of Cancer in Pediatric‐Onset Inflammatory Bowel Disease in Denmark and Finland

Objectives: Pediatric‐onset inflammatory bowel disease (pIBD) increases the risk of developing several different cancer forms. In this case‐control study, we aimed to assess the impact of medical treatment and disease activity on the risk of developing disease‐associated cancer (DAC) and treatment‐a...

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Published in:Journal of pediatric gastroenterology and nutrition Vol. 77; no. 1; pp. 55 - 61
Main Authors: Malham, Mikkel, Jansson, Sabine, Malmborg, Petter, Olén, Ola, Paerregaard, Anders, Virta, Lauri J., Jakobsen, Christian, Kolho, Kaija‐Leena, Wewer, Vibeke
Format: Journal Article
Language:English
Published: United States Lippincott Williams & Wilkins 01-07-2023
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Summary:Objectives: Pediatric‐onset inflammatory bowel disease (pIBD) increases the risk of developing several different cancer forms. In this case‐control study, we aimed to assess the impact of medical treatment and disease activity on the risk of developing disease‐associated cancer (DAC) and treatment‐associated cancer (TAC). Methods: In a previous study, we identified 27 cases of DAC (colorectal cancer, small bowel cancer, and cholangiocarcinoma) and 28 TAC (lymphoma and skin cancer) in 6689 patients with pIBD in Denmark and Finland during the period 1992–2015. In this study, the patient charts were reviewed manually. Cancer‐free patients from another population‐based pIBD cohort were included as controls. We recorded data on phenotype, medical treatment, surgery, and relapses. Logistic regression was used to estimate adjusted odds ratios (aOR) with 95% confidence intervals (95% CI) to estimate the relative risk. Results: We included 16 cases with DAC, 21 with TAC, and 331 controls. For DAC, lower frequencies of IBD‐relapses were associated with an increased risk of cancer (OR 0.2 [95% CI: 0.04–0.8]). For TAC, we found an increased risk in patients receiving thiopurines at any point during the follow‐up period (aOR: 11.7 [95% CI: 2.1–116.2]) and an association with proportion of follow‐up time being exposed to thiopurines (aOR 5.6 [95% CI: 1.1–31.5]). Conclusions: In this nation‐wide study, covering all pIBD patients from Denmark and Finland, we found that pIBD patients treated with thiopurines had an increased risk of TAC.
Bibliography:www.jpgn.org
O.O. has been PI for projects (unrelated to the present paper) at Karolinska Institutet financed by grants from Janssen, Takeda, AbbVie, Ferring, and Pfizer. Karolinska Institutet has received fees for lectures (OO) and participation on advisory boards (OO) from Janssen, Ferring, Bristol Myers Squibb, Galapagos and Takeda. The remaining authors report no conflicts of interest.
Supplemental digital content is available for this article. Direct URL citations appear in the printed text, and links to the digital files are provided in the HTML text of this article on the journal’s Web site
Sources of Funding: This work was supported by The Nordic Cancer Union [Grant number Rp15293, R217‐A13087].
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ISSN:0277-2116
1536-4801
1536-4801
DOI:10.1097/MPG.0000000000003781