Multitarget Stool DNA Screening in Clinical Practice: High Positive Predictive Value for Colorectal Neoplasia Regardless of Exposure to Previous Colonoscopy.


Journal

The American journal of gastroenterology
ISSN: 1572-0241
Titre abrégé: Am J Gastroenterol
Pays: United States
ID NLM: 0421030

Informations de publication

Date de publication:
04 2020
Historique:
pubmed: 19 2 2020
medline: 4 7 2020
entrez: 19 2 2020
Statut: ppublish

Résumé

Multitarget stool DNA (MT-sDNA) testing has grown as a noninvasive screening modality for colorectal cancer (CRC), but real-world clinical data are limited in the post-FDA approval setting. The effect of previous colonoscopy on MT-sDNA performance is not known. We aimed to evaluate findings of colorectal neoplasia (CRN) at diagnostic colonoscopy in patients with positive MT-sDNA testing, stratified by patient exposure to previous colonoscopy. We identified consecutive patients completing MT-sDNA testing over a 39-month period and reviewed the records of those with positive tests for neoplastic findings at diagnostic colonoscopy. MT-sDNA test positivity rate, adherence to diagnostic colonoscopy, and the positive predictive value (PPV) of MT-sDNA for any CRN and neoplastic subtypes were calculated. Of 16,469 MT-sDNA tests completed, testing returned positive in 2,326 (14.1%) patients. After exclusion of patients at increased risk for CRC, 1,801 patients remained, 1,558 (87%) of whom underwent diagnostic colonoscopy; 918 of 1,558 (59%) of these patients had undergone previous colonoscopy, whereas 640 (41%) had not. Any CRN was found in 1,046 of 1,558 patients (PPV = 67%). More neoplastic lesions were found in patients without previous colonoscopy (73%); however, the rates remained high among those who had undergone previous colonoscopy (63%, P < 0.0001). The large majority (79%) of patients had right-sided neoplasia. MT-sDNA has a high PPV for any CRN regardless of exposure to previous colonoscopy. Right-sided CRN was found at colonoscopy in most patients with positive MT-sDNA testing, representing a potential advantage over other currently available screening modalities for CRC.

Identifiants

pubmed: 32068535
doi: 10.14309/ajg.0000000000000546
pmc: PMC7127971
mid: NIHMS1548666
pii: 00000434-202004000-00020
doi:

Substances chimiques

DNA, Neoplasm 0

Types de publication

Journal Article Multicenter Study Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

608-615

Subventions

Organisme : NCI NIH HHS
ID : R37 CA214679
Pays : United States

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Auteurs

Jason D Eckmann (JD)

Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota, USA.

Derek W Ebner (DW)

Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota, USA.

Jamie Bering (J)

Department of Internal Medicine, Mayo Clinic, Scottsdale, Arizona, USA.

Allon Kahn (A)

Division of Gastroenterology and Hepatology, Mayo Clinic, Scottsdale, Arizona, USA.

Eduardo Rodriguez (E)

Division of Gastroenterology and Hepatology, Mayo Clinic, Scottsdale, Arizona, USA.

Mary E Devens (ME)

Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota, USA.

Kari L Lowrie (KL)

Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota, USA.

Karen Doering (K)

Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota, USA.

Sara Then (S)

Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota, USA.

Kelli N Burger (KN)

Division of Biomedical Statistics and Informatics, Mayo Clinic, Rochester, Minnesota, USA.

Douglas W Mahoney (DW)

Division of Biomedical Statistics and Informatics, Mayo Clinic, Rochester, Minnesota, USA.

David O Prichard (DO)

Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota, USA.
Division of Gastroenterology and Hepatology, Mayo Clinic Health System, LaCrosse, Wisconsin, USA.

Michael B Wallace (MB)

Division of Gastroenterology and Hepatology, Mayo Clinic, Jacksonville, Florida, USA.

Suryakanth R Gurudu (SR)

Division of Gastroenterology and Hepatology, Mayo Clinic, Scottsdale, Arizona, USA.

Lila J Finney (LJ)

Division of Health Care Policy and Research, Mayo Clinic, Rochester, Minnesota, USA.

Paul Limburg (P)

Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota, USA.

Barry Berger (B)

Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota, USA.
Exact Sciences, Madison, Wisconsin, USA.

David A Ahlquist (DA)

Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota, USA.

John B Kisiel (JB)

Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota, USA.

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