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Performance of the Fecal Immunochemical Test in Patients With a Family History of Colorectal Cancer.
Moosavi, Sarvee; Gentile, Laura; Gondara, Lovedeep; Mcgahan, Colleen; Enns, Robert Alan; Telford, Jennifer.
Afiliação
  • Moosavi S; Division of Gastroenterology and Hepatology, Department of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
  • Gentile L; British Columbia Cancer, Colon Cancer Screening Program.
  • Gondara L; British Columbia Cancer, Colon Cancer Screening Program.
  • Mcgahan C; British Columbia Cancer, Colon Cancer Screening Program.
  • Enns RA; Division of Gastroenterology and Hepatology, Department of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
  • Telford J; Division of Gastroenterology and Hepatology, Department of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
J Can Assoc Gastroenterol ; 3(6): 288-292, 2020 Dec.
Article em En | MEDLINE | ID: mdl-33241182
ABSTRACT

OBJECTIVE:

To assess the performance of a fecal immunochemical test (FIT) among participants of a population-based colorectal cancer (CRC) screening program with one or more first-degree relatives (FDR) with CRC.

METHODS:

Asymptomatic 50 to 74 years olds with a FDR diagnosed with CRC, enrolled in a colon screening program completed FIT (two samples, cut-off 20 µg Hemoglobin/gram feces) and underwent colonoscopy. FIT-interval CRCs were identified from the British Columbia cancer registry. Logistic regression analysis was used to identify variables associated with the detection of CRC and high-risk polyps (nonmalignant findings that required a 3-year surveillance colonoscopy) in those patients undergoing FIT and colonoscopy.

RESULTS:

Of the 1387 participants with a FDR with CRC, 1244 completed FIT with a positivity rate of 10.8%, 52 declined FIT but underwent colonoscopy and 90 declined screening. Seven CRCs were identified six in patients with a positive FIT, one in a patient who only had colonoscopy. No CRCs were found in patients with a negative FIT. The positive and negative predictive values of FIT in the detection of CRC were 4.8% and 100%, respectively. On multivariate logistic regression, positive FIT, and not type of family history, was the only variable associated with detection of CRC or high-risk polyps. At 2-year follow-up, there was no FIT interval cancer detected in the study cohort.

CONCLUSION:

FIT is more strongly associated with high-risk findings on colonoscopy than type of family history. FIT may be an alternative screening strategy to colonoscopy in individuals with a single FDR with CRC.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: J Can Assoc Gastroenterol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: J Can Assoc Gastroenterol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Canadá