Evidence map›Paper›PMID 42266054›Full record

ArticleRheumatology (Oxford, England)2026

Lifetime risk of malignancy in polymyalgia rheumatica: a population-based matched cohort study from southern Norway.

Stig Tengesdal, Øyvind Molberg, Øyvind Holme, Reza Ghiasvand, Jan Tore Gran, Geirmund Myklebust

Abstract read
In one paragraph

Article in Rheumatology (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Stig TengesdalDepartment of Research, Sorlandet Hospital, Kristiansand, Norway.ORCID 0000-0003-0994-756X
Øyvind MolbergDepartment of Rheumatology, Oslo University Hospital, Rikshospitalet, Oslo, Norway.
Øyvind HolmeDepartment of Research, Sorlandet Hospital, Kristiansand, Norway.
Reza GhiasvandCentre for Biostatistics and Epidemiology, Oslo University Hospital, Oslo, Norway.ORCID 0000-0002-5466-7308
Jan Tore GranDepartment of Rheumatology, Oslo University Hospital, Rikshospitalet, Oslo, Norway.
Geirmund MyklebustDepartment of Research, Sorlandet Hospital, Kristiansand, Norway.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesPrior studies examining the malignancy risk in polymyalgia rheumatica (PMR) have reported conflicting results, with some indicating an increased risk within 6-12 months after diagnosis. This study assessed malignancy risk over the lifetime and at different follow-up horizons in a population-based inception cohort of PMR patients.

methodsAll incident PMR cases (n = 296) in Aust-Agder County, Norway, between 1987 and 1997 were enrolled at diagnosis in a prospective, population-based study. Diagnosis was ascertained clinically by rheumatologists, with all cases fulfilling Bird's criteria. Each PMR case was matched by age, sex and residency to 15 random comparators (n = 4440). Cancer incidence data were obtained from the Cancer Registry of Norway. Participants were followed until first cancer diagnosis, death or 31 December 2024. Malignancy risk was estimated using Cox regression stratified on matched groups.

resultsThe mean age at PMR diagnosis was 72 years, 67.6% were female and 95.6% were deceased by 31 December 2024. Median follow-up was 14.1 years in PMR patients and 13.9 years among comparators. Following the index date, 70 PMR patients (23.6%) and 1104 comparators (24.9%) developed malignancy. PMR was not associated with an increased malignancy risk (hazard ratio 0.94; 95% CI: 0.73, 1.21), nor with significant excess risk in separate analyses by cancer type or by time since diagnosis.

conclusionIn this long-term follow-up of a population-based PMR inception cohort, we found no excess malignancy risk at any time from PMR diagnosis through the end of life. These findings reinforce the notion that PMR is not a cancer-associated disease.

Indexed as

NeoplasmsPolymyalgia RheumaticaAgedAged, 80 and overCohort StudiesFemaleFollow-Up StudiesHumansIncidenceMaleMiddle AgedNorwayProspective StudiesRegistriesRisk Factorscancerepidemiologymalignancypolymyalgia rheumatica

Identifiers

PMID42266054
PMCPMC13282711

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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.