Evidence map›Paper›PMID 40102189›Full record

ArticlePhotodermatology, photoimmunology & photomedicine2025

Photosensitizing Drugs and Risk of Skin Cancer in Women-A Prospective Population-Based Study.

Gustav Boelsgaard Christensen, Johan Kappelin, Jenny Sandgren, Kari Nielsen, Åsa Ingvar

Abstract read
In one paragraph

Article in Photodermatology, photoimmunology & photomedicine, 2025. 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

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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
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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

5 authors.

Gustav Boelsgaard ChristensenDepartment of Dermatology, Skåne University Hospital, Lund, Sweden.ORCID https://orcid.org/0000-0001-6797-1301
Johan KappelinLund University Skin Cancer Research Group, Dermatology, Department of Clinical Sciences, Lund, Lund University, Lund, Sweden.
Jenny SandgrenClinical Studies Sweden-Forum South, Skåne University Hospital, Lund, Sweden.
Kari NielsenDepartment of Dermatology, Skåne University Hospital, Lund, Sweden.
Åsa IngvarDepartment of Dermatology, Skåne University Hospital, Lund, Sweden.

Funding

Governmental funding for clinical researchHudfonden/Welander Finsen FoundationInga and John Hain Foundation for Medical ResearchRegional research support funds, Region SkåneS.R. Gorthon FoundationSwedish Cancer Society, Swedish Research Council, ERC advanced grant 2011-294576
6 · The paper itself

Abstract

backgroundSeveral widely used drugs have photosensitizing properties, and much research has been conducted to find associations between their use and the risk of developing cutaneous malignant melanoma (cM), basal cell carcinoma (BCC) or cutaneous squamous cell carcinoma (cSCC), often with conflicting results.

objectiveTo assess whether the use of commonly prescribed photosensitizing drugs increases skin cancer risk.

methodsAnalyses were performed using a large cohort of women, with prospectively collected information on phenotypic traits and sun exposure. Comprehensive information on pharmaceutical treatments and skin cancer occurrence was obtained through national registries. Drugs with photosensitizing properties were grouped according to the Anatomical Therapeutic Chemical system in nine groups, and associations between the use of such drugs were investigated using multivariable Cox regression analysis. The number of retrieved daily doses was analyzed to test the dose-response relationship.

resultsHormone replacement therapy significantly increased the risk of BCC (hazard ratio [HR] 1.24; 95% confidence interval [CI]: 1.11-1.39), cSCC (HR 1.23; 95% CI: 1.03-1.47) and cM (HR 1.31; 95% CI: 1.01-1.69), with estrogen driving this risk. There was a trend of increased risk of BCC and cM with higher doses of estrogen treatment. Subgroup analysis among those using diuretics showed that loop diuretics were associated with increased cSCC risk (HR 1.6; 95% CI: 1.3-2.0), including a positive association between risk and dose. Furthermore, increased risks of BCC (HR 1.25; 95% CI: 1.09-1.44) and cM (HR 1.41; 95% CI: 1.03-1.93) were associated with thiazide use. NSAIDs showed a possible curvilinear association to BCC and cSCC.

conclusionsEstrogen treatment increased the risk of all investigated skin cancers. Among those using diuretics, loop diuretics increased the risk of cSCC, and thiazide use increased the risk of BCC. We suggest that physicians should advise female patients prescribed estrogen, thiazides, or loop diuretics to limit their sun exposure.

Indexed as

Basal Cell CarcinomaCarcinoma, Squamous CellMelanomaPhotosensitizing AgentsSkin NeoplasmsAdultAgedCutaneous Malignant MelanomaFemaleHumansMiddle AgedProspective StudiesRisk FactorsPhotosensitizing Agentsbasal cell carcinomamelanomaphotosensitizing drugsprospectivesquamous cell carcinoma

Identifiers

PMID40102189
PMCPMC11919808

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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.