Evidence map›Paper›PMID 35333399›Full record

ArticleThe Australasian journal of dermatology2022

A long-term cohort study of acitretin for prevention of keratinocyte carcinoma in solid organ transplant recipients.

Katherine J Allnutt, Sara Vogrin, Jane Li, Michelle S Goh, Sarah Brennand, Rachael Davenport, Alvin H Chong

Open access · greenAbstract read
In one paragraph

Article in The Australasian journal of dermatology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

6 citing papers in PubMed, 12 citations in OpenAlex.

  1. Skin Cancer in Solid Organ Transplant Recipients: A Review.American journal of clinical dermatology · 2026
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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

7 authors at 2 institutions in 1 country.

Katherine J AllnuttSkin Health Institute, Carlton, Melbourne, Victoria, Australia.ORCID https://orcid.org/0000-0002-3465-9298
Sara VogrinFaculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Melbourne, Victoria, Australia.ORCID https://orcid.org/0000-0002-1597-9421
Jane LiSkin Health Institute, Carlton, Melbourne, Victoria, Australia.ORCID https://orcid.org/0000-0001-7150-4052
Michelle S GohSkin Health Institute, Carlton, Melbourne, Victoria, Australia.ORCID https://orcid.org/0000-0001-8063-8482
Sarah BrennandSkin Health Institute, Carlton, Melbourne, Victoria, Australia.
Rachael DavenportSkin Health Institute, Carlton, Melbourne, Victoria, Australia.ORCID https://orcid.org/0000-0002-4529-0641
Alvin H ChongSkin Health Institute, Carlton, Melbourne, Victoria, Australia.ORCID https://orcid.org/0000-0002-9577-0192
The University of Melbourne · AUSkin Health Institute · AU

Funding

Skin Health Institute, Carlton, Victoria, Australia
6 · The paper itself

Abstract

backgroundSolid organ transplant recipients (SOTR) are at high risk of keratinocyte carcinoma (KC). Long-term evidence for acitretin as chemoprophylaxis in this population is lacking.

objectiveTo determine the benefit of long-term acitretin for KC chemoprevention in SOTR.

methodsA retrospective cohort study of SOTR treated with acitretin at an Australian transplant dermatology clinic was performed. General estimating equations were used to evaluate change in rates of histologically confirmed KC in the 6-12 months prior to acitretin and following a minimum 6 months of treatment. A control group of patients within the same service was included, comprising SOTR who were not treated with acitretin.

resultsTwenty-two patients received acitretin treatment for at least 6 months, eighteen for at least 5 years and four for at least 9 years. The median KC rate pretreatment was 3.31 per year (IQR 1.93, 5.40). There was a significant reduction in the rate of KC in the first year of acitretin treatment (IRR 0.41, 95% CI 0.22, 0.76, P = 0.005), and this effect was observed for 5 years (IRR at 5 years 0.34, 95% CI 0.17, 0.67, P = 0.002). The control group had no statistically significant change in KC rate over time in the study.

conclusionsAcitretin appears to be well-tolerated and effective in reducing KC in SOTR for at least 5 years. Study limitations include its retrospective nature, small sample size and lack of blinding.

Indexed as

Carcinoma, Squamous CellOrgan TransplantationSkin NeoplasmsAcitretinAustraliaCohort StudiesHumansKeratinocytesRetrospective StudiesAcitretinacitretinchemopreventionimmunosuppressionorgan transplantsretinoidsskin neoplasmssquamous cell carcinoma

Identifiers

PMID35333399
PMCPMC9311671
OpenAlexW4220660783

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.