Evidence map›Paper›PMID 33928678›Full record

ArticleDigestive endoscopy : official journal of the Japan Gastroenterological Endoscopy Society2022

Clinicopathological features and risk factors for developing colorectal neoplasia in Hodgkin's lymphoma survivors.

Berbel L M Ykema, Lisanne S Rigter, Manon C W Spaander, Leon M G Moons, Tanya M Bisseling, Berthe M P Aleman, Evelien Dekker, Wieke H M Verbeek, Ernst J Kuipers, Jan Paul de Boer and 11 more

Open access · bronzeAbstract read
In one paragraph

Article in Digestive endoscopy : official journal of the Japan Gastroenterological Endoscopy Society, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 54% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

21 authors at 7 institutions in 1 country.

Berbel L M YkemaDepartment of, 1Gastroenterology and Hepatology, Netherlands Cancer Institute, Amsterdam, The Netherlands.ORCID https://orcid.org/0000-0002-0314-7986
Lisanne S RigterDepartment of, 1Gastroenterology and Hepatology, Netherlands Cancer Institute, Amsterdam, The Netherlands.ORCID https://orcid.org/0000-0002-1894-3440
Manon C W SpaanderDepartment of Gastroenterology and Hepatology, Erasmus Medical Center University Hospital, Rotterdam, The Netherlands.ORCID https://orcid.org/0000-0002-9103-9757
Leon M G MoonsDepartment of, Gastroenterology and Hepatology, University Medical Center Utrecht, Utrecht, The Netherlands.ORCID https://orcid.org/0000-0002-6913-9954
Tanya M BisselingDepartment of, Gastroenterology and Hepatology, Radboud University Medical Center, Nijmegen, The Netherlands.ORCID https://orcid.org/0000-0001-7976-7949
Berthe M P AlemanDepartment of, Radiation Oncology, Netherlands Cancer Institute, Amsterdam, The Netherlands.ORCID https://orcid.org/0000-0003-2306-6590
Evelien DekkerDepartment of Gastroenterology and Hepatology, Amsterdam University Medical Centers, Amsterdam, The Netherlands.ORCID https://orcid.org/0000-0002-4363-0745
Wieke H M VerbeekDepartment of, 1Gastroenterology and Hepatology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
Ernst J KuipersDepartment of Gastroenterology and Hepatology, Erasmus Medical Center University Hospital, Rotterdam, The Netherlands.ORCID https://orcid.org/0000-0002-0633-3098
Jan Paul de BoerDepartment of, Medical Oncology, Netherlands Cancer Institute, Amsterdam, The Netherlands.ORCID https://orcid.org/0000-0001-6218-6128
Pieternella J LugtenburgDepartment of, 8Hematology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.ORCID https://orcid.org/0000-0002-6735-8651
Cecile P M JanusDepartment of, Radiation Oncology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.ORCID https://orcid.org/0000-0003-3860-8698
Eefke J PetersenDepartment of, Hematology, University Medical Center Utrecht, Utrecht, The Netherlands.
Judith M RoesinkDepartment of, Radiation Oncology, University Medical Center Utrecht, Utrecht, The Netherlands.ORCID https://orcid.org/0000-0001-6586-0405
Richard W M van der MaazenDepartment of, Radiation Oncology, Radboud University Medical Center, Nijmegen, The Netherlands.ORCID https://orcid.org/0000-0003-0360-9172
Gerrit A MeijerDepartment of, Pathology, Netherlands Cancer Institute, Amsterdam, The Netherlands.ORCID https://orcid.org/0000-0003-0330-3130
Michael SchaapveldDepartment of, Epidemiology, Netherlands Cancer Institute, Amsterdam, The Netherlands.ORCID https://orcid.org/0000-0003-4390-7182
Flora E van LeeuwenDepartment of, Epidemiology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
Beatriz CarvalhoDepartment of, Pathology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
Petur SnaebjornssonDepartment of, Pathology, Netherlands Cancer Institute, Amsterdam, The Netherlands.ORCID https://orcid.org/0000-0002-1086-8108
Monique E van LeerdamDepartment of, 1Gastroenterology and Hepatology, Netherlands Cancer Institute, Amsterdam, The Netherlands.ORCID https://orcid.org/0000-0002-5719-3208
The Netherlands Cancer Institute · NLUniversity Medical Center Utrecht · NLErasmus MC · NLErasmus MC Cancer Institute · NLRadboud University Nijmegen · NLAmsterdam University Medical Centers · NLLeiden University Medical Center · NL

Funding

Dutch Digestive Disease Foundation FP 14-04
6 · The paper itself

Abstract

backgroundHodgkin's lymphoma (HL) survivors treated with abdominal radiotherapy and/or procarbazine have an increased risk of developing colorectal neoplasia.

aimsWe evaluated the clinicopathological characteristics and risk factors for developing (advanced) neoplasia (AN) in HL survivors.

methodsIn all, 101 HL survivors (median age 51 years, median age of HL diagnosis 25 years) underwent colonoscopy and 350 neoplasia and 44 AN (classified as advanced adenomas/serrated lesions or colorectal cancer), mostly right-sided, were detected, as published previously. An average-risk asymptomatic cohort who underwent screening colonoscopy were controls (median age 60 years). Clinicopathological characteristics of AN were evaluated in both groups. Mismatch repair (MMR) status was assessed using immunohistochemistry (MLH1/MSH2/MSH6/PMS2). Logistic regression analysis was performed to evaluate the risk factors for AN in HL survivors, including age at HL diagnosis and interval between HL and colonoscopy.

resultsIn 101 colonoscopies in HL survivors, AN was primarily classified based on polyp size ≥10 mm, whereas (high-grade)dysplasia was more often seen in AN in controls. An interval between HL diagnosis and colonoscopy >26 years was associated with more AN compared with an interval of <26 years, with an odds ratio for AN of 3.8 (95% confidence interval 1.4-9.1) (p < 0.01). All 39 AN that were assessed were MMR proficient.

conclusionsColorectal neoplasia in HL survivors differ from average-risk controls; classification AN was primarily based on polyp size (≥10 mm) in HL survivors. Longer follow-up between HL diagnosis and colonoscopy was associated with a higher prevalence of AN in HL survivors.

Indexed as

Colorectal NeoplasmsHodgkin DiseaseAdultColonoscopyHumansMiddle AgedRisk FactorsSurvivorscancer survivorscolonoscopycolorectal neoplasmsDNA mismatch repairHodgkin's lymphoma

Identifiers

PMID33928678
PMCPMC9290704
OpenAlexW3158083406

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.