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

Author:

Malham Mikkel123,Jansson Sabine12,Malmborg Petter45,Olén Ola45,Paerregaard Anders12,Virta Lauri J.6,Jakobsen Christian12,Kolho Kaija-Leena7,Wewer Vibeke12

Affiliation:

1. Department of Paediatric and Adolescence Medicine, Copenhagen University Hospital – Amager and Hvidovre, Hvidovre, Denmark

2. Copenhagen Centre for Inflammatory Bowel Disease in Children, Adolescents and Adults, Copenhagen University Hospital – Amager and Hvidovre, Hvidovre, Denmark

3. Department of Paediatric and Adolescence Medicine, Copenhagen University Hospital – Rigshospitalet, Copenhagen, Denmark

4. Sachs’ Children and Youth Hospital, Stockholm, Sweden

5. Clinical Epidemiology Division, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden

6. Research Department, Social Insurance Institution of Finland, Turku, Finland

7. Children’s Hospital, Helsinki University Hospital, Helsinki, Finland.

Abstract

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.

Publisher

Wiley

Subject

Gastroenterology,Pediatrics, Perinatology and Child Health

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