Sessile Serrated Adenomas in Young Patients may have Limited Risk of Malignant Progression.


Journal

Journal of clinical gastroenterology
ISSN: 1539-2031
Titre abrégé: J Clin Gastroenterol
Pays: United States
ID NLM: 7910017

Informations de publication

Date de publication:
03 2019
Historique:
pubmed: 24 3 2018
medline: 18 7 2020
entrez: 24 3 2018
Statut: ppublish

Résumé

To provide preliminary evidence that sessile serrated adenomas (SSA) are low-risk polyps in young patients. SSAs are the dominant polyp of the serrated neoplasia pathway and as such are the precursor of up to 20% of colorectal carcinomas (CRC). Up to 90% of these cancers are expected to harbor a BRAF mutation. SSAs are being diagnosed with increasing frequency in young patients, placing a significant burden on colonoscopic services. Evidence to direct the surveillance intervals for these young patients is not available. We utilized 2 patient cohorts comprising (1) a consecutive series of patients who underwent outpatient colonoscopy through a tertiary hospital and (2) a consecutive series of resection specimens for CRC processed through a gastrointestinal pathology service. The prevalence of SSAs by age was determined in the patients undergoing colonoscopy and compared with the ages of patients with BRAF mutated CRC in the pathology series. The prevalence of SSAs was similar irrespective of age. By comparison, BRAF mutated CRCs were very rare (3.8% of cases) in patients younger than 50 years of age and uncommon (9.3% of cases) in patients younger than 60 years of age, but increased to 39.8% in patients older than 80 years of age. These results suggest that SSAs develop at a young age, but have a prolonged dwell time and are unlikely to develop into cancer in patients younger than 60 years of age. These findings highlight the need for further targeted research to determine the most appropriate surveillance intervals for young patients with sporadic SSAs.

Sections du résumé

GOALS
To provide preliminary evidence that sessile serrated adenomas (SSA) are low-risk polyps in young patients.
BACKGROUND
SSAs are the dominant polyp of the serrated neoplasia pathway and as such are the precursor of up to 20% of colorectal carcinomas (CRC). Up to 90% of these cancers are expected to harbor a BRAF mutation. SSAs are being diagnosed with increasing frequency in young patients, placing a significant burden on colonoscopic services. Evidence to direct the surveillance intervals for these young patients is not available.
STUDY
We utilized 2 patient cohorts comprising (1) a consecutive series of patients who underwent outpatient colonoscopy through a tertiary hospital and (2) a consecutive series of resection specimens for CRC processed through a gastrointestinal pathology service. The prevalence of SSAs by age was determined in the patients undergoing colonoscopy and compared with the ages of patients with BRAF mutated CRC in the pathology series.
RESULTS
The prevalence of SSAs was similar irrespective of age. By comparison, BRAF mutated CRCs were very rare (3.8% of cases) in patients younger than 50 years of age and uncommon (9.3% of cases) in patients younger than 60 years of age, but increased to 39.8% in patients older than 80 years of age.
CONCLUSIONS
These results suggest that SSAs develop at a young age, but have a prolonged dwell time and are unlikely to develop into cancer in patients younger than 60 years of age. These findings highlight the need for further targeted research to determine the most appropriate surveillance intervals for young patients with sporadic SSAs.

Identifiants

pubmed: 29570172
doi: 10.1097/MCG.0000000000001014
doi:

Substances chimiques

BRAF protein, human EC 2.7.11.1
Proto-Oncogene Proteins B-raf EC 2.7.11.1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e113-e116

Commentaires et corrections

Type : CommentIn

Auteurs

Mark Bettington (M)

Envoi Specialist Pathologists.
School of Medicine, University of Queensland.
The Conjoint Gastroenterology Laboratory, QIMR Berghofer Medical Research Institute.

Ian Brown (I)

Envoi Specialist Pathologists.
Department of Anatomical Pathology, Central Laboratory, Pathology Queensland.

Christophe Rosty (C)

Envoi Specialist Pathologists.
School of Medicine, University of Queensland.
Department of Pathology, University of Melbourne, Melbourne, Vic., Australia.

Neal Walker (N)

Envoi Specialist Pathologists.
School of Medicine, University of Queensland.

Cheng Liu (C)

School of Medicine, University of Queensland.
The Conjoint Gastroenterology Laboratory, QIMR Berghofer Medical Research Institute.

John Croese (J)

Department of Gastroenterology and Hepatology, The Prince Charles Hospital.
The Centre for Biodiscovery and Molecular Developmental Therapeutics, James Cook University, Cairns, Qld.

Tony Rahman (T)

Department of Gastroenterology and Hepatology, The Prince Charles Hospital.

Sally-Ann Pearson (SA)

The Conjoint Gastroenterology Laboratory, QIMR Berghofer Medical Research Institute.

Diane McKeone (D)

The Conjoint Gastroenterology Laboratory, QIMR Berghofer Medical Research Institute.

Barbara Leggett (B)

School of Medicine, University of Queensland.
The Conjoint Gastroenterology Laboratory, QIMR Berghofer Medical Research Institute.
Department of Gastroenterology and Hepatology, The Royal Brisbane and Women's Hospital.

Vicki Whitehall (V)

School of Medicine, University of Queensland.
The Conjoint Gastroenterology Laboratory, QIMR Berghofer Medical Research Institute.
Department of Chemical Pathology, Pathology Queensland, Brisbane.

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