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ArticleFamilial cancer2025

Comparative insight: hereditary colorectal cancer registries in Iran, Singapore, and South Africa.

Ladan Goshayeshi, Ernest Wencong Eu, Raj Ramesar, Paul Goldberg, Yu Bin Tan, Ursula Algar, Rutharra Ghayadthri Manisekaran, Shao-Tzu Li, Rebecca Caeser, Adam Boutall and 3 more

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Familial cancer, 2025. 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
–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

1 citing paper in PubMed.

  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

13 authors.

Ladan Goshayeshi *Department of Gastroenterology and Hepatology, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, 91779-48564, Iran.
Ernest Wencong Eu *Department of Colorectal Surgery, Singapore General Hospital, Singapore, Singapore.
Raj Ramesar *UCT/MRC Genomic and Precision Medicine Research Unit, Division of Human Genetics, Department of Pathology, Faculty of Health Sciences, Institute of Infectious Diseases and Molecular Medicine, University of Cape Town, Cape Town, South Africa.
Paul GoldbergDivision of Surgical Gastroenterology, Departments of Medicine and Surgery, UCT/Groote Schuur Hospital, Cape Town, South Africa.
Yu Bin TanCancer Genetics Service, Division of Medical Oncology, National Cancer Centre Singapore, Singapore, Singapore.
Ursula AlgarDivision of Surgical Gastroenterology, Departments of Medicine and Surgery, UCT/Groote Schuur Hospital, Cape Town, South Africa.
Rutharra Ghayadthri ManisekaranCancer Genetics Service, Division of Medical Oncology, National Cancer Centre Singapore, Singapore, Singapore.
Shao-Tzu LiCancer Genetics Service, Division of Medical Oncology, National Cancer Centre Singapore, Singapore, Singapore.
Rebecca CaeserCancer Genetics Service, Division of Medical Oncology, National Cancer Centre Singapore, Singapore, Singapore.
Adam BoutallDivision of Surgical Gastroenterology, Departments of Medicine and Surgery, UCT/Groote Schuur Hospital, Cape Town, South Africa.
Lena GoshayeshiStem Cell Biology and Regenerative Medicine Research Group, Research Institute of Biotechnology, Ferdowsi University of Mashhad, Mashhad, Iran.
Kevin J Monahan *Lynch Syndrome Clinic, The Centre for Familial Intestinal Cancer, St Marks Hospital, London, UK.
Joanne Ngeow *Cancer Genetics Service, Division of Medical Oncology, National Cancer Centre Singapore, Singapore, Singapore. joanne.ngeow@ntu.edu.sg.

Funding

National Institute for Medical Research Development 978991
6 · The paper itself

Abstract

This study compares three hereditary colorectal cancer (CRC) registries-the Iranian Hereditary Colorectal Cancer Registry (IHCCR), the Singapore Polyposis Registry (SPR), and the University of Cape Town Familial CRC Registry-to illuminate diverse approaches to identification, management, and research across different healthcare systems. Each registry, while emphasizing patient diversity, employed unique strategies reflecting available resources and epidemiological contexts. The IHCCR, leveraging WES, revealed considerable genetic heterogeneity, including novel mutations. The SPR, a nationalized service, focused on structured surveillance and management of FAP and other polyposis syndromes, highlighting the challenges of cultural conservatism and limited public awareness. The UCT registry, initially concentrating on Lynch syndrome, expanded to encompass other hereditary CRC syndromes, revealing a high prevalence of these conditions within the South African population. All three registries encountered challenges related to access to genetic testing and early diagnosis. The registries' combined experiences underscore the critical need for integrated, culturally sensitive strategies combining genetic testing, enhanced surveillance, and family-based management to improve outcomes for individuals and families affected by hereditary CRC. Future efforts should focus on addressing disparities in access to care and expanding research to improve understanding and management of this complex disease.

Indexed as

Adenomatous Polyposis ColiColorectal NeoplasmsColorectal Neoplasms, Hereditary NonpolyposisRegistriesAdultFemaleGenetic TestingHumansIranMaleMiddle AgedSingaporeSouth AfricaCancer prevention & early detectionGenetic syndromesHereditary colorectal cancer registries

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.