Risk of Early Colorectal Cancers Needs to Be Considered in Inflammatory Bowel Disease Care.


Journal

Digestive diseases and sciences
ISSN: 1573-2568
Titre abrégé: Dig Dis Sci
Pays: United States
ID NLM: 7902782

Informations de publication

Date de publication:
08 2019
Historique:
received: 14 08 2018
accepted: 20 02 2019
pubmed: 1 3 2019
medline: 8 2 2020
entrez: 1 3 2019
Statut: ppublish

Résumé

Current guidelines recommend starting colorectal cancer (CRC) surveillance 8-10 years after inflammatory bowel disease (IBD) onset. Recent studies report that the incidence of CRC within 8-10 years of IBD onset (i.e., early CRC) ranges from 12 to 42%. To describe the current prevalence of early CRC in a tertiary care center IBD cohort with CRC and to identify associated risk factors. We performed a single-center observational study of IBD patients diagnosed with CRC from 2005 to 2015. We compared characteristics of patients with early CRC (diagnosis of CRC within 8 years of initial IBD onset) to those with CRC diagnosed later in their IBD course. Ninety-three patients met inclusion criteria. Eleven (11.8%) patients developed CRC within 8 years of initial IBD onset. On multivariable logistic regression, age greater than 28 at IBD onset (adjusted OR 12.0; 95% CI 2.30, 62.75) and tobacco use (adjusted OR 8.52; 95% CI 1.38, 52.82) were significant predictors of early CRC. A validation cohort confirmed calibration and discrimination of the model. One out of every eight IBD patients with CRC developed their malignancy prior to the currently recommended timeframe for the initiation of surveillance colonoscopy. IBD onset at 28 years or older and tobacco use were identified as predictors of early CRC. Early CRC should be considered in discussions of cancer surveillance in this population. Prospective cohort studies are necessary to further analyze the impact of early CRC in IBD.

Sections du résumé

BACKGROUND
Current guidelines recommend starting colorectal cancer (CRC) surveillance 8-10 years after inflammatory bowel disease (IBD) onset. Recent studies report that the incidence of CRC within 8-10 years of IBD onset (i.e., early CRC) ranges from 12 to 42%.
AIMS
To describe the current prevalence of early CRC in a tertiary care center IBD cohort with CRC and to identify associated risk factors.
METHODS
We performed a single-center observational study of IBD patients diagnosed with CRC from 2005 to 2015. We compared characteristics of patients with early CRC (diagnosis of CRC within 8 years of initial IBD onset) to those with CRC diagnosed later in their IBD course.
RESULTS
Ninety-three patients met inclusion criteria. Eleven (11.8%) patients developed CRC within 8 years of initial IBD onset. On multivariable logistic regression, age greater than 28 at IBD onset (adjusted OR 12.0; 95% CI 2.30, 62.75) and tobacco use (adjusted OR 8.52; 95% CI 1.38, 52.82) were significant predictors of early CRC. A validation cohort confirmed calibration and discrimination of the model.
CONCLUSIONS
One out of every eight IBD patients with CRC developed their malignancy prior to the currently recommended timeframe for the initiation of surveillance colonoscopy. IBD onset at 28 years or older and tobacco use were identified as predictors of early CRC. Early CRC should be considered in discussions of cancer surveillance in this population. Prospective cohort studies are necessary to further analyze the impact of early CRC in IBD.

Identifiants

pubmed: 30815820
doi: 10.1007/s10620-019-05554-1
pii: 10.1007/s10620-019-05554-1
doi:

Types de publication

Journal Article Observational Study Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

2273-2279

Subventions

Organisme : NCATS NIH HHS
ID : UL1 TR000457
Pays : United States

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Auteurs

Shirley Cohen-Mekelburg (S)

Division of Gastroenterology and Hepatology, Michigan Medicine, 3912 Taubman Center, 1500 E. Medical Center Drive, SPC 5362, Ann Arbor, MI, 48109, USA. shcohen@umich.edu.

Yecheskel Schneider (Y)

Division of Gastroenterology and Hepatology, University of Pennsylvania, Philadelphia, PA, USA.

Stephanie Gold (S)

Department of Medicine, NewYork Presbyterian Weill Cornell Medicine, New York, NY, USA.

Gaurav Ghosh (G)

Department of Medicine, NewYork Presbyterian Weill Cornell Medicine, New York, NY, USA.

Russell Rosenblatt (R)

Division of Gastroenterology and Hepatology, NewYork Presbyterian Weill Cornell Medicine, New York, NY, USA.

Kaveh Hajifathalian (K)

Division of Gastroenterology and Hepatology, NewYork Presbyterian Weill Cornell Medicine, New York, NY, USA.

Ellen Scherl (E)

Division of Gastroenterology and Hepatology, NewYork Presbyterian Weill Cornell Medicine, New York, NY, USA.

Felice Schnoll-Sussman (F)

Division of Gastroenterology and Hepatology, NewYork Presbyterian Weill Cornell Medicine, New York, NY, USA.

Philip Katz (P)

Division of Gastroenterology and Hepatology, NewYork Presbyterian Weill Cornell Medicine, New York, NY, USA.

Adam Steinlauf (A)

Division of Gastroenterology and Hepatology, Mount Sinai Hospital, New York, NY, USA.

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Classifications MeSH