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Randomized Trial of Facilitated Adherence to Screening Colonoscopy vs Sequential Fecal-Based Blood Test.
Zauber, Ann G; Winawer, Sidney J; O'Brien, Michael J; Mills, Glenn M; Allen, John I; Feld, Andrew D; Jordan, Paul A; Fleisher, Martin; Orlow, Irene; Meester, Reinier G S; Lansdorp-Vogelaar, Iris; Rutter, Carolyn M; Knudsen, Amy B; Mandelson, Margaret; Shaukat, Aasma; Mendelsohn, Robin B; Hahn, Anne I; Lobaugh, Stephanie M; Soto Palmer, Brittany; Serrano, Victoria; Kumar, Julie R; Fischer, Sara E; Chen, Jennifer C; Bayuga-Miller, Sharon; Kuk, Deborah; O'Connell, Kelli; Church, Timothy R.
Afiliação
  • Zauber AG; Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York. Electronic address: zaubera@mskcc.org.
  • Winawer SJ; Gastroenterology, Hepatology, and Nutrition Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
  • O'Brien MJ; Department of Pathology and Laboratory Medicine, Boston University Medical Center, Boston, Massachusetts.
  • Mills GM; Feist-Weiller Cancer Center, Shreveport, Louisiana.
  • Allen JI; Division of Gastroenterology and Hepatology, Department of Medicine, University of Michigan School of Medicine, Ann Arbor, Michigan.
  • Feld AD; Department of Gastroenterology, Kaiser Permanente Washington, Seattle, Washington.
  • Jordan PA; Department of Medicine, Louisiana State University Health, Shreveport, Louisiana.
  • Fleisher M; Department of Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Orlow I; Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Meester RGS; Department of Public Health, Erasmus University Medical Center, Rotterdam, The Netherlands.
  • Lansdorp-Vogelaar I; Department of Public Health, Erasmus University Medical Center, Rotterdam, The Netherlands.
  • Rutter CM; Biostatistics Program, Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Hutchinson Institute for Cancer Outcomes Research, Seattle, Washington.
  • Knudsen AB; Institute for Technology Assessment, Massachusetts General Hospital, Boston, Massachusetts; Harvard Medical School, Boston, Massachusetts.
  • Mandelson M; Cancer Institute Virginia Mason Medical Center, Seattle, Washington.
  • Shaukat A; Division of Gastroenterology, Department of Medicine Environmental Health Sciences, University of Minnesota School of Public Health, Minneapolis, Minnesota; Masonic Cancer Center, University of Minnesota, Minneapolis, Minnesota; Division of Gastroenterology, Department of Medicine, NYU Langone Healt
  • Mendelsohn RB; Gastroenterology, Hepatology, and Nutrition Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Hahn AI; Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Lobaugh SM; Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Soto Palmer B; CVS Health, Woonsocket, Rhode Island.
  • Serrano V; Regeneron Pharmaceuticals, Tarrytown, New York.
  • Kumar JR; Investigative Initiative Trials and Compassionate Use Studies, Novartis, East Hanover, New Jersey.
  • Fischer SE; Department of Government, Georgetown University, Washington, District of Columbia.
  • Chen JC; Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Bayuga-Miller S; Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Kuk D; Flatiron Health, New York, New York.
  • O'Connell K; Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Church TR; Division of Gastroenterology, Department of Medicine Environmental Health Sciences, University of Minnesota School of Public Health, Minneapolis, Minnesota; Masonic Cancer Center, University of Minnesota, Minneapolis, Minnesota.
Gastroenterology ; 165(1): 252-266, 2023 Jul.
Article em En | MEDLINE | ID: mdl-36948424
BACKGROUND & AIMS: Colorectal cancer (CRC) screening guidelines include screening colonoscopy and sequential high-sensitivity fecal occult blood testing (HSgFOBT), with expectation of similar effectiveness based on the assumption of similar high adherence. However, adherence to screening colonoscopy compared with sequential HSgFOBT has not been reported. In this randomized clinical trial, we assessed adherence and pathology findings for a single screening colonoscopy vs sequential and nonsequential HSgFOBTs. METHODS: Participants aged 40-69 years were enrolled at 3 centers representing different clinical settings. Participants were randomized into a single screening colonoscopy arm vs sequential HSgFOBT arm composed of 4-7 rounds. Initial adherence to screening colonoscopy and sequential adherence to HSgFOBT, follow-up colonoscopy for positive HSgFOBT tests, crossover to colonoscopy, and detection of advanced neoplasia or large serrated lesions (ADN-SERs) were measured. RESULTS: There were 3523 participants included in the trial; 1761 and 1762 participants were randomized to the screening colonoscopy and HSgFOBT arms, respectively. Adherence was 1473 (83.6%) for the screening colonoscopy arm vs 1288 (73.1%) for the HSgFOBT arm after 1 round (relative risk [RR], 1.14; 95% CI, 1.10-1.19; P ≤ .001), but only 674 (38.3%) over 4 sequential HSgFOBT rounds (RR, 2.19; 95% CI, 2.05-2.33). Overall adherence to any screening increased to 1558 (88.5%) in the screening colonoscopy arm during the entire study period and 1493 (84.7%) in the HSgFOBT arm (RR, 1.04; 95% CI, 1.02-1.07). Four hundred thirty-six participants (24.7%) crossed over to screening colonoscopy during the first 4 rounds. ADN-SERs were detected in 121 of the 1473 participants (8.2%) in the colonoscopy arm who were adherent to protocol in the first 12 months of the study, whereas detection of ADN-SERs among those who were not sequentially adherent (n = 709) to HSgFOBT was subpar (0.6%) (RR, 14.72; 95% CI, 5.46-39.67) compared with those who were sequentially adherent (3.3%) (n = 647) (RR, 2.52; 95% CI, 1.61-3.98) to HSgFOBT in the first 4 rounds. When including colonoscopies from HSgFOBT patients who were never positive yet crossed over (n = 1483), 5.5% of ADN-SERs were detected (RR, 1.50; 95% CI, 1.15-1.96) in the first 4 rounds. CONCLUSIONS: Observed adherence to sequential rounds of HSgFOBT was suboptimal compared with a single screening colonoscopy. Detection of ADN-SERs was inferior when nonsequential HSgFOBT adherence was compared with sequential adherence. However, the greatest number of ADN-SERs was detected among those who crossed over to colonoscopy and opted to receive a colonoscopy. The effectiveness of an HSgFOBT screening program may be enhanced if crossover to screening colonoscopy is permitted. CLINICALTRIALS: gov, Number: NCT00102011.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Sangue Oculto Tipo de estudo: Clinical_trials / Diagnostic_studies / Etiology_studies / Guideline / Prognostic_studies / Screening_studies Limite: Humans Idioma: En Revista: Gastroenterology Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Sangue Oculto Tipo de estudo: Clinical_trials / Diagnostic_studies / Etiology_studies / Guideline / Prognostic_studies / Screening_studies Limite: Humans Idioma: En Revista: Gastroenterology Ano de publicação: 2023 Tipo de documento: Article