Personalised surveillance for serrated polyposis syndrome: results from a prospective 5-year international cohort study.
Adenomatous Polyposis Coli
/ diagnosis
Aged
Cohort Studies
Colonoscopy
/ methods
Colorectal Neoplasms
/ diagnosis
Female
Follow-Up Studies
Humans
Incidence
Male
Medical Overuse
/ prevention & control
Middle Aged
Netherlands
/ epidemiology
Population Surveillance
/ methods
Prevalence
Prospective Studies
Risk Factors
Spain
/ epidemiology
colonic polyps
colorectal cancer
polyposis
Journal
Gut
ISSN: 1468-3288
Titre abrégé: Gut
Pays: England
ID NLM: 2985108R
Informations de publication
Date de publication:
01 2020
01 2020
Historique:
received:
18
12
2018
revised:
27
03
2019
accepted:
28
03
2019
pubmed:
15
4
2019
medline:
18
12
2019
entrez:
15
4
2019
Statut:
ppublish
Résumé
Serrated polyposis syndrome (SPS) is associated with an increased risk of colorectal cancer (CRC). International guidelines recommend surveillance intervals of 1-2 years. However, yearly surveillance likely leads to overtreatment for many. We prospectively assessed a surveillance protocol aiming to safely reduce the burden of colonoscopies. Between 2013 and 2018, we enrolled SPS patients from nine Dutch and Spanish hospitals. Patients were surveilled using a protocol appointing either a 1-year or 2-year interval after each surveillance colonoscopy, based on polyp burden. Primary endpoint was the 5-year cumulative incidence of CRC and advanced neoplasia (AN) during surveillance. We followed 271 SPS patients for a median of 3.6 years. During surveillance, two patients developed CRC (cumulative 5-year incidence 1.3%[95% CI 0% to 3.2%]). The 5-year AN incidence was 44% (95% CI 37% to 52%), and was lower for patients with SPS type III (26%) than for patients diagnosed with type I (53%) or type I and III (59%, p<0.001). Most patients were recommended a 2-year interval, and those recommended a 2-year interval were not at increased risk of AN: AN incidence after a 2-year recommendation was 15.6% compared with 24.4% after a 1-year recommendation (OR 0.57, p=0.08). Risk stratification substantially reduced colonoscopy burden while achieving CRC incidence similar to previous studies. AN incidence is considerable in SPS patients, but extension of surveillance intervals was not associated with increased AN in those identified as low-risk by the protocol. We identified SPS type III patients as low-risk group that might benefit from even less frequent surveillance. The study was registered on http://www.trialregister.nl; trial-ID NTR4609.
Sections du résumé
BACKGROUND AND AIMS
Serrated polyposis syndrome (SPS) is associated with an increased risk of colorectal cancer (CRC). International guidelines recommend surveillance intervals of 1-2 years. However, yearly surveillance likely leads to overtreatment for many. We prospectively assessed a surveillance protocol aiming to safely reduce the burden of colonoscopies.
METHODS
Between 2013 and 2018, we enrolled SPS patients from nine Dutch and Spanish hospitals. Patients were surveilled using a protocol appointing either a 1-year or 2-year interval after each surveillance colonoscopy, based on polyp burden. Primary endpoint was the 5-year cumulative incidence of CRC and advanced neoplasia (AN) during surveillance.
RESULTS
We followed 271 SPS patients for a median of 3.6 years. During surveillance, two patients developed CRC (cumulative 5-year incidence 1.3%[95% CI 0% to 3.2%]). The 5-year AN incidence was 44% (95% CI 37% to 52%), and was lower for patients with SPS type III (26%) than for patients diagnosed with type I (53%) or type I and III (59%, p<0.001). Most patients were recommended a 2-year interval, and those recommended a 2-year interval were not at increased risk of AN: AN incidence after a 2-year recommendation was 15.6% compared with 24.4% after a 1-year recommendation (OR 0.57, p=0.08).
CONCLUSION
Risk stratification substantially reduced colonoscopy burden while achieving CRC incidence similar to previous studies. AN incidence is considerable in SPS patients, but extension of surveillance intervals was not associated with increased AN in those identified as low-risk by the protocol. We identified SPS type III patients as low-risk group that might benefit from even less frequent surveillance.
TRIAL REGISTRATION NUMBER
The study was registered on http://www.trialregister.nl; trial-ID NTR4609.
Identifiants
pubmed: 30981990
pii: gutjnl-2018-318134
doi: 10.1136/gutjnl-2018-318134
pmc: PMC6943249
doi:
Banques de données
NTR
['NTR4609']
Types de publication
Clinical Trial
Journal Article
Multicenter Study
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
112-121Commentaires et corrections
Type : ErratumIn
Informations de copyright
© Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY. Published by BMJ.
Déclaration de conflit d'intérêts
Competing interests: ED: I have endoscopic equipment on loan of Olympus and Fujifilm, and received a research grant from Fujifilm. I have also received an honorarium for consultancy from Fujifilm, Tillotts and Olympus and a speaker’s fee from Olympus and Roche. FB: I have endoscopic equipment on loan of Fujifilm, and received an honorarium for consultancy from Sysmex and a speaker’s fee from Norgine. MP: I have received a research grant from Fujifilm, consultancy fee from Norgine and speaker’s fee from Olympus, Norgine, Casen Recordati and Janssen.
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