TY - JOUR
T1 - Association between indefinite dysplasia and advanced neoplasia in patients with inflammatory bowel diseases undergoing surveillance
AU - Mahmoud, Remi
AU - Shah, Shailja C.
AU - Torres, Joana
AU - Castaneda, Daniel
AU - Glass, Jason
AU - Elman, Jordan
AU - Kumar, Akash
AU - Axelrad, Jordan
AU - Harpaz, Noam
AU - Ullman, Thomas
AU - Colombel, Jean-Frédéric
AU - Oldenburg, Bas
AU - Itzkowitz, Steven H.
N1 - Funding Information:
Conflicts of interest These authors disclose the following: J. Torres has served as a consultant for Takeda and received speaker fees from Takeda, AbbVie, and Ferring. T. Ullman has served as consultant for Salix/Valeant and for Janssen. J.-F. Colombel has served as consultant, advisory board member, or speaker for AbbVie, Amgen, Boehringer-Ingelheim, Celgene Corporation, Celltrion, Enterome, Ferring, Genentech, Janssen and Janssen, Lilly, Medimmune, Merck & Co, Pfizer, PPM Services, Protagonist, Second Genome, Seres, Shire, Takeda, Theradiag, and Theravance Biopharma; has stock options in Intestinal Biotech Development, Genfit; and has received research grants from AbbVie, Takeda, and Janssen and Janssen. Noam Harpaz has served as a consultant for Celgene, AbbVie, and Lilly USA. B. Oldenburg has served as consultant for MSD, Takeda, AbbVie, Ferring, Cablon, and Janssen; has received unrestricted grants from AbbVie, Ferring, Dr. Falk, MSD, Takeda, and Janssen; and has received speakers’ fees from Ferring and MSD. The remaining authors disclose no conflicts. Funding S.C.S. is partly funded by K12 HS026395-01 and an AGA Research Scholar Award.
Funding Information:
Funding S.C.S. is partly funded by K12 HS026395-01 and an AGA Research Scholar Award.
Publisher Copyright:
© 2020 AGA Institute
PY - 2020/6
Y1 - 2020/6
N2 - Background & Aims: Little is known about the clinical significance of indefinite dysplasia (IND) in patients with inflammatory bowel diseases (IBD) undergoing colonoscopic surveillance for colorectal neoplasia. Methods: We conducted a retrospective cohort analysis of 492 patients with colonic IBD for 8 or more years or concomitant primary sclerosing cholangitis, with no history of advanced colorectal neoplasia (high-grade dysplasia or colorectal cancer) or colectomy, undergoing colorectal neoplasia surveillance at a tertiary IBD referral center from 2001 through 2017. Subjects received consistent histopathologic grading of dysplasia. We collected data on time to development of (advanced) colorectal neoplasia or colectomy using Kaplan Meier methods. We identified factors independently associated with (advanced) colorectal neoplasia with multivariable Cox regression analysis. Results: After 2149 person-years of follow-up, 53 patients (10.8%) received a diagnosis of IND without prior or synchronous low-grade dysplasia (LGD). Compared to patients without dysplasia, patients with IND had a significantly higher risk of advanced colorectal neoplasia (adjusted hazard ratio, 6.85; 95% CI, 1.78–26.4) and colorectal neoplasia (adjusted hazard ratio, 3.25; 95% CI, 1.50–7.05), but not colectomy (P = .78). Compared to IND, LGD was associated with a significantly higher risk of advanced colorectal neoplasia (P = .05). Following a diagnosis of no dysplasia, IND only, or LGD, the incidence rates of advanced colorectal neoplasia were 0.4% per patient-year, 3.1% per patient-year, and 8.4% per patient-year, respectively. Conclusions: In a retrospective analysis of patients with IBD undergoing colorectal neoplasia surveillance with consistent histopathologic grading of dysplasia, IND was independently associated with a significant increase in risk of advanced colorectal neoplasia. These findings require validation and if confirmed, a reappraisal of the colorectal neoplasia surveillance guidelines.
AB - Background & Aims: Little is known about the clinical significance of indefinite dysplasia (IND) in patients with inflammatory bowel diseases (IBD) undergoing colonoscopic surveillance for colorectal neoplasia. Methods: We conducted a retrospective cohort analysis of 492 patients with colonic IBD for 8 or more years or concomitant primary sclerosing cholangitis, with no history of advanced colorectal neoplasia (high-grade dysplasia or colorectal cancer) or colectomy, undergoing colorectal neoplasia surveillance at a tertiary IBD referral center from 2001 through 2017. Subjects received consistent histopathologic grading of dysplasia. We collected data on time to development of (advanced) colorectal neoplasia or colectomy using Kaplan Meier methods. We identified factors independently associated with (advanced) colorectal neoplasia with multivariable Cox regression analysis. Results: After 2149 person-years of follow-up, 53 patients (10.8%) received a diagnosis of IND without prior or synchronous low-grade dysplasia (LGD). Compared to patients without dysplasia, patients with IND had a significantly higher risk of advanced colorectal neoplasia (adjusted hazard ratio, 6.85; 95% CI, 1.78–26.4) and colorectal neoplasia (adjusted hazard ratio, 3.25; 95% CI, 1.50–7.05), but not colectomy (P = .78). Compared to IND, LGD was associated with a significantly higher risk of advanced colorectal neoplasia (P = .05). Following a diagnosis of no dysplasia, IND only, or LGD, the incidence rates of advanced colorectal neoplasia were 0.4% per patient-year, 3.1% per patient-year, and 8.4% per patient-year, respectively. Conclusions: In a retrospective analysis of patients with IBD undergoing colorectal neoplasia surveillance with consistent histopathologic grading of dysplasia, IND was independently associated with a significant increase in risk of advanced colorectal neoplasia. These findings require validation and if confirmed, a reappraisal of the colorectal neoplasia surveillance guidelines.
KW - Carcinogenesis
KW - Crohn's Disease
KW - Neoplasm
KW - Ulcerative colitis
UR - http://www.scopus.com/inward/record.url?scp=85084664838&partnerID=8YFLogxK
U2 - 10.1016/j.cgh.2019.08.032
DO - 10.1016/j.cgh.2019.08.032
M3 - Article
C2 - 31446183
AN - SCOPUS:85084664838
SN - 1542-3565
VL - 18
SP - 1518-1527.e3
JO - Clinical Gastroenterology and Hepatology
JF - Clinical Gastroenterology and Hepatology
IS - 7
ER -