Biology and Clinical Implications of Fecal Occult Blood Test Screen-Detected Colorectal Cancer.


Journal

JNCI cancer spectrum
ISSN: 2515-5091
Titre abrégé: JNCI Cancer Spectr
Pays: England
ID NLM: 101721827

Informations de publication

Date de publication:
05 01 2022
Historique:
accepted: 11 11 2021
received: 06 07 2021
revised: 11 07 2021
entrez: 14 6 2022
pubmed: 15 6 2022
medline: 18 6 2022
Statut: ppublish

Résumé

Fecal occult blood test (FOBT)-based screening for colorectal cancer (CRC) reduces mortality, with earlier stage at diagnosis a prominent feature. Other characteristics of FOBT screen-detected cancers and any implications for clinical management have not been well explored. We examined a multisite clinical registry to compare the characteristics and outcomes of FOBT screen-detected CRC via the Australian National Bowel Cancer Screening Program (NBCSP), which is offered biennially to individuals aged 50-74 years, and age-matched non-screen-detected CRC in the same registry. All statistical tests were 2-sided. Odds ratios (ORs) were calculated using the Baptista-Pike method, and hazard ratios via the log-rank method. Of 7153 registry patients diagnosed June 1, 2006, to June 30, 2020, 4142 (57.9%) were aged between 50 and 74 years. Excluding 406 patients with non-NBCSP screen-detected cancers and 35 patients with unknown method of detection, 473 (12.8%) were screen detected via the NBCSP, and 3228 (87.2%) were non-screen detected. Screen-detected patients were younger (mean age = 62.4 vs 64.2 years; P < .001) and more medically fit (OR for ASA score 1-2 = 1.91, 95% confidence interval [CI] = 1.51 to 2.41; P < .001). Pathologic characteristics within each stage favored the screen-detected patients. Stage III screen-detected colon cancers were more likely to receive adjuvant therapy (OR = 3.58, 95% CI = 1.52 to 8.36; P = .002). Screen-detected patients had superior relapse-free (hazard ratio = 0.41, 95% CI = 0.29 to 0.60; P < .001) and overall survival (hazard ratio = 0.22, 95% CI = 0.15 to 0.35; P < .001), which was maintained in matched stage comparisons and multivariable analysis. Beyond stage at diagnosis, multiple other factors associated with a favorable outcome are observed in FOBT screen-detected CRC. Given the substantial stage-by-stage differences in survival outcomes, if independently confirmed, individualized adjuvant therapy and surveillance strategies could be warranted for FOBT screen-detected cancers.

Sections du résumé

BACKGROUND
Fecal occult blood test (FOBT)-based screening for colorectal cancer (CRC) reduces mortality, with earlier stage at diagnosis a prominent feature. Other characteristics of FOBT screen-detected cancers and any implications for clinical management have not been well explored.
METHODS
We examined a multisite clinical registry to compare the characteristics and outcomes of FOBT screen-detected CRC via the Australian National Bowel Cancer Screening Program (NBCSP), which is offered biennially to individuals aged 50-74 years, and age-matched non-screen-detected CRC in the same registry. All statistical tests were 2-sided. Odds ratios (ORs) were calculated using the Baptista-Pike method, and hazard ratios via the log-rank method.
RESULTS
Of 7153 registry patients diagnosed June 1, 2006, to June 30, 2020, 4142 (57.9%) were aged between 50 and 74 years. Excluding 406 patients with non-NBCSP screen-detected cancers and 35 patients with unknown method of detection, 473 (12.8%) were screen detected via the NBCSP, and 3228 (87.2%) were non-screen detected. Screen-detected patients were younger (mean age = 62.4 vs 64.2 years; P < .001) and more medically fit (OR for ASA score 1-2 = 1.91, 95% confidence interval [CI] = 1.51 to 2.41; P < .001). Pathologic characteristics within each stage favored the screen-detected patients. Stage III screen-detected colon cancers were more likely to receive adjuvant therapy (OR = 3.58, 95% CI = 1.52 to 8.36; P = .002). Screen-detected patients had superior relapse-free (hazard ratio = 0.41, 95% CI = 0.29 to 0.60; P < .001) and overall survival (hazard ratio = 0.22, 95% CI = 0.15 to 0.35; P < .001), which was maintained in matched stage comparisons and multivariable analysis.
CONCLUSIONS
Beyond stage at diagnosis, multiple other factors associated with a favorable outcome are observed in FOBT screen-detected CRC. Given the substantial stage-by-stage differences in survival outcomes, if independently confirmed, individualized adjuvant therapy and surveillance strategies could be warranted for FOBT screen-detected cancers.

Identifiants

pubmed: 35699496
pii: 6502287
doi: 10.1093/jncics/pkab100
pmc: PMC8857921
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press.

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Auteurs

Shehara Mendis (S)

Personalised Oncology Division, Walter & Eliza Hall Institute, Parkville, VIC, Australia.
Department of Medical Oncology, Sunshine Hospital, Western Health, St Albans, VIC, Australia.

Wei Hong (W)

Personalised Oncology Division, Walter & Eliza Hall Institute, Parkville, VIC, Australia.
Faculty of Medicine & Health Sciences, The University of Melbourne, Parkville, VIC, Australia.

Sumitra Ananda (S)

Personalised Oncology Division, Walter & Eliza Hall Institute, Parkville, VIC, Australia.
Department of Medical Oncology, Sunshine Hospital, Western Health, St Albans, VIC, Australia.
Department of Medical Oncology, Peter MacCallum Cancer Centre, Parkville, VIC, Australia.

Ian Faragher (I)

Department of Colorectal Surgery, Footscray Hospital, Western Health, Footscray, VIC, Australia.

Ian Jones (I)

Department of Colorectal Surgery, The Royal Melbourne Hospital, Parkville, VIC, Australia.
Department of Surgery, The University of Melbourne, Parkville, VIC, Australia.

Matthew Croxford (M)

Department of Colorectal Surgery, Footscray Hospital, Western Health, Footscray, VIC, Australia.

Malcolm Steel (M)

Department of Colorectal Surgery, Box Hill Hospital, Eastern Health, Box Hill, VIC, Australia.

Azim Jalali (A)

Personalised Oncology Division, Walter & Eliza Hall Institute, Parkville, VIC, Australia.
Department of Medical Oncology, Sunshine Hospital, Western Health, St Albans, VIC, Australia.

Grace Gard (G)

Personalised Oncology Division, Walter & Eliza Hall Institute, Parkville, VIC, Australia.
Department of Medical Oncology, Sunshine Hospital, Western Health, St Albans, VIC, Australia.

Yat Hang To (YH)

Personalised Oncology Division, Walter & Eliza Hall Institute, Parkville, VIC, Australia.
Faculty of Medicine & Health Sciences, The University of Melbourne, Parkville, VIC, Australia.

Margaret Lee (M)

Personalised Oncology Division, Walter & Eliza Hall Institute, Parkville, VIC, Australia.
Department of Medical Oncology, Sunshine Hospital, Western Health, St Albans, VIC, Australia.
Department of Medical Oncology, Eastern Health, Box Hill, VIC, Australia.
Eastern Health Clinical School, Monash University, Box Hill, VIC, Australia.

Suzanne Kosmider (S)

Department of Medical Oncology, Sunshine Hospital, Western Health, St Albans, VIC, Australia.

Rachel Wong (R)

Personalised Oncology Division, Walter & Eliza Hall Institute, Parkville, VIC, Australia.
Department of Medical Oncology, Eastern Health, Box Hill, VIC, Australia.
Eastern Health Clinical School, Monash University, Box Hill, VIC, Australia.

Jeanne Tie (J)

Personalised Oncology Division, Walter & Eliza Hall Institute, Parkville, VIC, Australia.
Department of Medical Oncology, Sunshine Hospital, Western Health, St Albans, VIC, Australia.
Faculty of Medicine & Health Sciences, The University of Melbourne, Parkville, VIC, Australia.

Peter Gibbs (P)

Personalised Oncology Division, Walter & Eliza Hall Institute, Parkville, VIC, Australia.
Department of Medical Oncology, Sunshine Hospital, Western Health, St Albans, VIC, Australia.
Faculty of Medicine & Health Sciences, The University of Melbourne, Parkville, VIC, Australia.
Department of Medical Oncology, The Royal Melbourne Hospital, Parkville, VIC, Australia.

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