Colitis-Associated Colorectal Cancer in Patients with Inflammatory Bowel Diseases in a Tertiary Referral Center: A Propensity Score Matching Analysis.

colitis-associated colorectal cancer colorectal cancer inflammatory bowel diseases

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
07 Feb 2022
Historique:
received: 01 12 2021
revised: 02 02 2022
accepted: 03 02 2022
entrez: 15 2 2022
pubmed: 16 2 2022
medline: 16 2 2022
Statut: epublish

Résumé

Inflammatory bowel disease (IBD) is a risk factor in developing colitis-associated colorectal cancer (CA-CRC). CA-CRC causes the death of about 15% IBD patients and the risk is 1.5-2.4 fold higher among IBD sufferers than in the general population. The dysplasia CA-CRC develops in a different mechanism in comparison to sporadic colorectal cancer (CRC). This study aimed at evaluating the surgical treatment and its outcomes as well as 5-year survival rates in the CA-CRC and sporadic CRC patients. This single-center, retrospective, propensity score-matched case-control study was conducted with 2204 patients operated on due to primary CRC, who were hospitalized from 2003 to 2019. The CA-CRC group consisted of 49 patients with CRC in the course of IBD. The sporadic CRC group was selected with the propensity score matching technique and comprised 98 patients with sporadic CRC who did not have clinical or histopathological features characteristic for IBD. CA-CRC is characterized by a more aggressive clinical course. Surgical treatment of CA-CRC involves more palliative operations and is related with a higher risk of perioperative and postoperative complications. Further studies of CA-CRC risk factor stratification and the development of molecular markers hold promise in reducing CRC in IBD patients in the future were warranted.

Sections du résumé

BACKGROUND BACKGROUND
Inflammatory bowel disease (IBD) is a risk factor in developing colitis-associated colorectal cancer (CA-CRC). CA-CRC causes the death of about 15% IBD patients and the risk is 1.5-2.4 fold higher among IBD sufferers than in the general population. The dysplasia CA-CRC develops in a different mechanism in comparison to sporadic colorectal cancer (CRC). This study aimed at evaluating the surgical treatment and its outcomes as well as 5-year survival rates in the CA-CRC and sporadic CRC patients.
MATERIALS AND METHODS METHODS
This single-center, retrospective, propensity score-matched case-control study was conducted with 2204 patients operated on due to primary CRC, who were hospitalized from 2003 to 2019. The CA-CRC group consisted of 49 patients with CRC in the course of IBD. The sporadic CRC group was selected with the propensity score matching technique and comprised 98 patients with sporadic CRC who did not have clinical or histopathological features characteristic for IBD.
RESULTS RESULTS
CA-CRC is characterized by a more aggressive clinical course. Surgical treatment of CA-CRC involves more palliative operations and is related with a higher risk of perioperative and postoperative complications. Further studies of CA-CRC risk factor stratification and the development of molecular markers hold promise in reducing CRC in IBD patients in the future were warranted.

Identifiants

pubmed: 35160321
pii: jcm11030866
doi: 10.3390/jcm11030866
pmc: PMC8836563
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Kasper Maryńczak (K)

Department of General and Oncological Surgery, Faculty of Medicine, Medical University of Lodz, 251 Pomorska, 92-213 Lodz, Poland.

Jakub Włodarczyk (J)

Department of General and Oncological Surgery, Faculty of Medicine, Medical University of Lodz, 251 Pomorska, 92-213 Lodz, Poland.
Department of Biochemistry, Medical University of Lodz, Mazowiecka 6/8, 92-215 Lodz, Poland.

Zofia Sabatowska (Z)

Department of General and Oncological Surgery, Faculty of Medicine, Medical University of Lodz, 251 Pomorska, 92-213 Lodz, Poland.

Adam Dziki (A)

Department of General and Colorectal Surgery, Medical University of Lodz, 113 Żeromskiego, 90-624 Lodz, Poland.

Łukasz Dziki (Ł)

Department of General and Oncological Surgery, Faculty of Medicine, Medical University of Lodz, 251 Pomorska, 92-213 Lodz, Poland.

Marcin Włodarczyk (M)

Department of General and Oncological Surgery, Faculty of Medicine, Medical University of Lodz, 251 Pomorska, 92-213 Lodz, Poland.

Classifications MeSH