Evidence map›Paper›PMID 36444504›Full record

ArticleInternational journal of cancer2023

Factors associated with interval colorectal cancer after negative FIT: Results of two screening rounds in the Dutch FIT-based CRC screening program.

Emilie C H Breekveldt, Esther Toes-Zoutendijk, Hilliene J van de Schootbrugge-Vandermeer, Lucie de Jonge, Arthur I Kooyker, Manon C W Spaander, Anneke J van Vuuren, Folkert J van Kemenade, Christian Ramakers, Evelien Dekker and 3 more

Open access · hybridAbstract read
In one paragraph

Article in International journal of cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.9field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 20 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 4 institutions in 1 country.

Emilie C H BreekveldtDepartment of Public Health, Erasmus MC University Medical Center, Rotterdam, The Netherlands.ORCID 0000-0002-2503-7323
Esther Toes-ZoutendijkDepartment of Public Health, Erasmus MC University Medical Center, Rotterdam, The Netherlands.ORCID 0000-0003-4001-2949
Hilliene J van de Schootbrugge-VandermeerDepartment of Public Health, Erasmus MC University Medical Center, Rotterdam, The Netherlands.ORCID 0000-0002-0543-4225
Lucie de JongeDepartment of Public Health, Erasmus MC University Medical Center, Rotterdam, The Netherlands.ORCID 0000-0001-5718-1058
Arthur I KooykerDepartment of Public Health, Erasmus MC University Medical Center, Rotterdam, The Netherlands.ORCID 0000-0001-6324-0931
Manon C W SpaanderDepartment of Gastroenterology and Hepatology, Erasmus MC University Medical Center, Rotterdam, The Netherlands.ORCID 0000-0002-9103-9757
Anneke J van VuurenDepartment of Gastroenterology and Hepatology, Erasmus MC University Medical Center, Rotterdam, The Netherlands.ORCID 0000-0002-0624-3623
Folkert J van KemenadeDepartment of Pathology, Erasmus MC University Medical Center, Rotterdam, The Netherlands.ORCID 0000-0002-4225-4354
Christian RamakersDepartment of Clinical Chemistry, Erasmus MC University Medical Center, Rotterdam, The Netherlands.ORCID 0000-0002-5537-6211
Evelien DekkerDepartment of Gastroenterology and Hepatology, Amsterdam University Medical Centers-Academic Medical Center, Amsterdam, The Netherlands.ORCID 0000-0002-4363-0745
Iris D NagtegaalDepartment of Pathology, Radboud University Medical Center, Nijmegen, The Netherlands.ORCID 0000-0003-0887-4127
Monique E van LeerdamDepartment of Gastroenterology and Hepatology, Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.ORCID 0000-0002-5719-3208
Iris Lansdorp-VogelaarDepartment of Public Health, Erasmus MC University Medical Center, Rotterdam, The Netherlands.ORCID 0000-0002-9438-2753
Erasmus MC · NLAmsterdam UMC Location University of Amsterdam · NLLeiden University Medical Center · NLRadboud University Nijmegen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The interval colorectal cancer (CRC) rate after negative fecal immunochemical testing (FIT) is an important quality indicator of CRC screening programs. We analyzed the outcomes of two rounds of the FIT-based CRC screening program in the Netherlands, using data from individuals who participated in FIT-screening from 2014 to 2017. Data of individuals with one prior negative FIT (first round) or two prior negative FITs (first and second round) were included. Outcomes included the incidence of interval CRC in FIT-negative participants (<47 μg Hb/g feces [μg/g]), FIT-sensitivity, and the probability of detecting an interval CRC by fecal hemoglobin concentration (f-Hb). FIT-sensitivity was estimated using the detection method and the proportional incidence method (based on expected CRC incidence). Logistic regression analysis was performed to estimate whether f-Hb affects probability of detecting interval CRC, adjusted for sex- and age-differences. Incidence of interval CRC was 10.4 per 10 000 participants after the first and 9.6 after the second screening round. FIT-sensitivity based on the detection method was 84.4% (95%CI 83.8-85.0) in the first and 73.5% (95% CI 71.8-75.2) in the second screening round. The proportional incidence method resulted in a FIT-sensitivity of 76.4% (95%CI 73.3-79.6) in the first and 79.1% (95%CI 73.7-85.3) in the second screening round. After one negative FIT, participants with f-Hb just below the cut-off (>40-46.9 μg/g) had a higher probability of detecting an interval CRC (OR 16.9; 95%CI: 14.0-20.4) than had participants with unmeasurable f-Hb (0-2.6 μg/g). After two screening rounds, the odds ratio for interval CRC was 12.0 (95%CI: 7.8-17.6) for participants with f-Hb just below the cut-off compared with participants with unmeasurable f-Hb. After both screening rounds, the Dutch CRC screening program had a low incidence of interval CRC and an associated high FIT-sensitivity. Our findings suggest there is a potential for further optimizing CRC screening programs with the use of risk-stratified CRC screening based on prior f-Hb.

Indexed as

Colorectal NeoplasmsEarly Detection of CancerColonoscopyFecesHemoglobinsHumansMass ScreeningOccult BloodHemoglobinscolorectal cancercolorectal cancer screeningfecal immunochemical testing

Identifiers

PMID36444504
PMCPMC10107864
OpenAlexW4310208875

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.