Evidence map›Paper›PMID 41454185›Full record

ArticleBritish journal of cancer2026

Lifetime risk of solid tumors and leukemia in Down Syndrome: a population-based Swedish matched cohort study.

Alexandra Wachtmeister, Benedicte Bang, Ida Nordgren, Anna Martling, Bertil Johansson, Yunxia Lu, Anna Skarin Nordenvall, Giorgio Tettamanti, Ann Nordgren

Abstract read
In one paragraph

Article in British journal of cancer, 2026. 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

9 authors.

Alexandra WachtmeisterDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden. alexandra.wachtmeister@ki.se.ORCID http://orcid.org/0000-0003-0553-1460
Benedicte BangDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.ORCID http://orcid.org/0000-0001-6907-4954
Ida NordgrenDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.ORCID http://orcid.org/0009-0009-3000-361X
Anna MartlingDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.ORCID http://orcid.org/0000-0001-5998-4735
Bertil JohanssonDepartment of Clinical Genetics, Pathology, and Molecular Diagnostics, Laboratory Medicine, Region Skåne, Lund, Sweden.ORCID http://orcid.org/0000-0001-8829-4813
Yunxia LuDepartment of Population Health and Disease Prevention & Department of Epidemiology and Biostatistics, Joe C. Wen School of Population & Public Health, University of California, Irvine, CA, USA.ORCID http://orcid.org/0000-0002-1201-7729
Anna Skarin NordenvallDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.ORCID http://orcid.org/0000-0003-3034-9222
Giorgio TettamantiDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.ORCID http://orcid.org/0000-0002-5210-7219
Ann NordgrenDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.ORCID http://orcid.org/0000-0003-3285-4281

Funding

Barncancerfonden (Swedish Childhood Cancer Foundation) PR2022-0027Cancerfonden (Swedish Cancer Society) 22 2057 PJVetenskapsrådet (Swedish Research Council) 2021-02860Vetenskapsrådet (Swedish Research Council) 2022-06312.379
6 · The paper itself

Abstract

backgroundIndividuals with Down syndrome have an elevated risk of childhood leukaemia and are suggested to have a reduced risk of solid tumours in adulthood. However, it remains unclear which cancer subtypes contribute to this pattern and the lifetime cancer risk.

methodsThis Swedish population-based matched cohort study investigated age- and subtype-specific cancer risks in Down syndrome. National healthcare registers were used to include 9742 individuals with Down syndrome, born in Sweden between 1930-2017. Each individual was matched by birth year, sex, and birth county to 50 comparisons. Hazard ratios (HRs) and 95% confidence intervals (95% CI) were calculated using Cox proportional hazard models.

resultsChildren with Down syndrome had a 20-fold increased risk of acute lymphoblastic leukaemia (ALL), and nearly a 500-fold increased risk of acute myeloid leukaemia (AML) before the age of 5. In contrast, individuals with Down syndrome had an overall lower risk of solid tumours, with significantly decreased risks for breast, prostate, lung, colorectal, gynaecological cancers, and melanoma, in adults. However, an increased risk was observed for testicular cancer and chondrosarcoma/chondroblastoma.

conclusionWe present the most comprehensive profile of cancer risk in Down syndrome, aiming to guide clinical practices, encourage tailored surveillance recommendations, and incite research on chromosome 21's role in oncogenesis.

Indexed as

Down SyndromeLeukemiaNeoplasmsAdolescentAdultAgedChildChild, PreschoolCohort StudiesFemaleHumansInfantInfant, NewbornMaleMiddle AgedPrecursor Cell Lymphoblastic Leukemia-Lymphoma

Identifiers

PMID41454185
PMCPMC12905194

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.