Evidence map›Paper›PMID 39323004›Full record

ArticleColorectal disease : the official journal of the Association of Coloproctology of Great Britain and Ireland2024

Faecal haemoglobin concentration and colorectal cancer site, stage and grade in a symptomatic cohort.

Nicholas G Farkas, James O'Brien, James Norman, Jackie Steinke, Kai Shing Yu, Martin Whyte, Iain Jourdan, Tim Rockall, Sally C Benton

Abstract read
In one paragraph

Article in Colorectal disease : the official journal of the Association of Coloproctology of Great Britain and Ireland, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. Faecal haemoglobin concentration and colorectal cancer site, stage and grade in a symptomatic cohort.Colorectal disease : the official journal of the Association of Coloproctology of Great Britain and Ireland · 2024
    Article
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

9 authors.

Nicholas G FarkasMinimal Access Therapy and Training Unit (MATTU), Royal Surrey Hospital NHS Foundation Trust, Guildford, UK.ORCID 0000-0003-4216-4786
James O'BrienMinimal Access Therapy and Training Unit (MATTU), Royal Surrey Hospital NHS Foundation Trust, Guildford, UK.
James NormanMinimal Access Therapy and Training Unit (MATTU), Royal Surrey Hospital NHS Foundation Trust, Guildford, UK.
Jackie SteinkeMinimal Access Therapy and Training Unit (MATTU), Royal Surrey Hospital NHS Foundation Trust, Guildford, UK.
Kai Shing YuMinimal Access Therapy and Training Unit (MATTU), Royal Surrey Hospital NHS Foundation Trust, Guildford, UK.ORCID 0000-0003-0098-1876
Martin WhyteFaculty of Health and Medical Sciences, University of Surrey, Guildford, UK.
Iain JourdanMinimal Access Therapy and Training Unit (MATTU), Royal Surrey Hospital NHS Foundation Trust, Guildford, UK.
Tim RockallMinimal Access Therapy and Training Unit (MATTU), Royal Surrey Hospital NHS Foundation Trust, Guildford, UK.
Sally C BentonDepartment of Clinical Biochemistry, Royal Surrey County Hospital, Berkshire and Surrey Pathology Services, Guildford, Surrey, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimMinimal evidence exists regarding faecal immunochemical tests (FITs) for colorectal cancer (CRC) site, stage and grade in symptomatic patients. The primary aim is to determine any association between faecal haemoglobin concentration (f-Hb) (analysed with OC-Sensor™ Pledia) and these prognostic factors. The secondary aim is to determine the association between f-Hb and anaemia, microcytosis and iron deficiency (Hb, mean corpuscular volume [MCV] and ferritin). METHODOLOGY: Symptomatic 2-week wait CRC patients with FIT were included (July 2019-October 2022). Median f-Hb and interquartile range according to sex, stage, grade and site (right-sided, caecum to transverse colon, R-CRC; left-sided, splenic flexure to rectum, L-CRC) were compared using the Mann-Whitney U test. Hb, MCV and ferritin were categorized into two groups and the median f-Hb was compared using the Mann-Whitney U test.

resultsIn all, 114 patients (57 women, 57 men) were studied; 46 had R-CRC (f-Hb = 113 μg Hb/g) and 68 had L-CRC (f-Hb = 342 μg Hb/g) (P = 0.07). Sixty-nine were moderately differentiated CRC (f-Hb = 183 μg Hb/g) and 29 were poorly differentiated (f-Hb = 866 μg Hb/g) (P = 0.04). By T-stage, 35 were early (T1/2) (f-Hb = 170 μg Hb/g) and 79 were advanced (T3/4) (f-Hb = 200 μg Hb/g) (P = 0.06). The relationship between f-Hb and Hb, MCV and ferritin was not significant. Poorly differentiated (P = 0.04) and later stage (P = 0.02) R-CRC had significantly lower f-Hb compared to L-CRC.

conclusionsRight-sided CRC is associated with lower f-Hb than left. Poorly differentiated and later staged L-CRC had higher median f-Hb. These data add to existing evidence suggesting that FIT may be less sensitive for right-sided CRC. Strategies to mitigate the potential for missed or FIT-negative right-sided CRC are required.

Indexed as

Colorectal NeoplasmsFecesHemoglobinsNeoplasm GradingNeoplasm StagingAgedAnemiaCohort StudiesErythrocyte IndicesFemaleFerritinsHumansMaleMiddle AgedOccult BloodPrognosisFerritinsHemoglobinscolorectal cancerfaecal immunochemical testgradesitestage

Identifiers

PMID39323004
PMCPMC11649872

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LicenceCC BY
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Registered trials

None linked

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.