Evidence map›Paper›PMID 40836309›Full record

ArticleAdvances in rheumatology (London, England)2025

Prevalence of solid tumors and lymphoma in the Brazilian Sjögren's Disease Registry (BRAS): an important concern for clinical practice.

Virginia Fernandes Moça Trevisani, Fabiola Reis de Oliveira, Sandra Gofinet Pasoto, Laura Caldas, Roberta de Almeida Pernambuco, Alisson Pugliesi, Leandro Augusto Tanure, Juliana Markus, Maria Lúcia Lemos Lopes, Aysa César Pinheiro and 14 more

Abstract read
In one paragraph

Article in Advances in rheumatology (London, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

24 authors.

Virginia Fernandes Moça TrevisaniUniversidade Federal de São Paulo, São Paulo, SP, Brazil. vmoca@uol.com.br.ORCID http://orcid.org/0000-0002-7180-6285
Fabiola Reis de OliveiraHospital das Clínicas da Faculdade de Medicina de Ribeirão Preto da USP, Ribeirão Preto, SP, Brazil.
Sandra Gofinet PasotoHospital das Clínicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brazil.
Laura CaldasUniversidade Federal de São Paulo, São Paulo, SP, Brazil.
Roberta de Almeida PernambucoInstituto de Assistência Médica ao Servidor Público Estadual, São Paulo, SP, Brazil.
Alisson PugliesiHospital das Clínicas da Universidade Estadual de Campinas, Campinas, SP, Brazil.
Leandro Augusto TanureHospital das Clínicas da Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.
Juliana MarkusHospital de Clínicas, Faculdade de Medicina da Universidade Federal de Uberlândia, Uberlândia, MG, Brazil.
Maria Lúcia Lemos LopesIrmandade da Santa Casa de Misericórdia de Porto Alegre, Universidade Federal de Ciências da Saúde de Porto Alegre, Porto Alegre, RS, Brazil.
Aysa César PinheiroHospital das Clínicas da Universidade Federal de Pernambuco, Recife, PE, Brazil.
Vanessa HaxHospital de Clínicas de Porto Alegre da Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.
Aiessa Zanchett FedrigoHospital Universitário Evangélico Mackenzie, Curitiba, PR, Brazil.
Sandra Lúcia Euzébio RibeiroUniversidade Federal do Amazonas, Manaus, AM, Brazil.
Karina Gatz CapobiancoHospital Moinhos de Vento, Porto Alegre, RS, Brazil.
Giovanna Sant'Ana PetterleHospital Universitário Júlio Müller, Universidade Federal de Mato Grosso, Cuiabá, MT, Brazil.
Diego Ustárroz CantaliHospital São Lucas, Pontifícia Universidade Católica do Rio Grande do Sul, Avenida Ipiranga, Porto Alegre, RS, Brazil.
Rafael CoradinIrmandade da Santa Casa de Misericórdia de Porto Alegre, Universidade Federal de Ciências da Saúde de Porto Alegre, Porto Alegre, RS, Brazil.
Gustavo Pafume de SáHospital Universitário Júlio Müller, Universidade Federal de Mato Grosso, Cuiabá, MT, Brazil.
Ketty Lisie Libardi MachadoHospital Universitário Cassiano Antônio Moraes, Universidade Federal do Espírito Santo, Vitória, ES, Brazil.
Bianca RosaHospital Universitário Cassiano Antônio Moraes, Universidade Federal do Espírito Santo, Vitória, ES, Brazil.
Raíssa Dudienas Domingues PereiraHospital das Clínicas da Universidade Estadual de Campinas, Campinas, SP, Brazil.
Samira Tatiyama MiyamotoDepartamento de Educação Integrada em Saúde, Universidade Federal do Espírito Santo, Vitória, ES, Brazil.
Nelson Carvas JuniorUniversidade São Paulo, UNIP, São Paulo, SP, Brazil.
Valéria ValimHospital Universitário Cassiano Antônio Moraes, Universidade Federal do Espírito Santo, Vitória, ES, Brazil.

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico #303116/2022-6
6 · The paper itself

Abstract

backgroundAbout 5–10% of patients with Sjögren’s Disease (SjD) will develop non-Hodgkin’s lymphoma, with a 16 to 44 increased risk compared to the general population. The relationship between SjD and other types of cancer is poorly described in the literature.

aimTo characterize patients with SjD from the Brazilian Sjögren’s Disease Registry (BRAS) who developed hematological and solid neoplasms, analyzing the organ primarily involved, subtypes, occurrence of metastatic disease, timing of diagnosis and correlation with demographic, serologic aspects, and labial salivary gland inflammation.

methodsAmong consecutive patients included in the Brazilian Sjögren’s Disease Registry (BRAS) and fulfilling the 2002 or 2016 classification criteria for SjD, those who developed neoplasia were retrospectively identified and categorized according to the National Cancer Institute (Ministry of Health, Brazil).

results1,010 patients were included; of them, 975 were women (96.5%), with an average age of 55.6 ± 13.6 years. Disease duration was 11.9 ± 7.9 years. We found that 114 out of 1,010 patients (11.3%) had cancer, with a higher prevalence in those over 55 years old (p < 0.001). The most prevalent malignancies were skin cancer [24/858 (2.7%)], breast cancer [27/1010 (2.6%)], lymphoma [15/1010 (1.5%)], and thyroid cancer [8/1010 (0.8%)]. Further, 0.9% of patients had more than one type of cancer. Cancer diagnosis followed SjD diagnosis in 66.7% of lymphoma cases, 53.6% of other malignancies, and 75.0% of skin cancer. The presence of cancer was associated with age (OR 1.04). In the case of skin cancer, the duration of SjD was an additional risk factor (OR 1.08). For thyroid cancer, inflammation of the labial minor salivary glands was identified as an associated risk factor (OR 10.1).

conclusionsOther types of cancer were more prevalent than lymphoma in our population of SjD patients. Breast neoplasia emerged as the most prevalent after skin cancer, and thyroid cancer was the second most prevalent solid neoplasia. Aging, disease duration and labial salivary gland inflammation were associated risk factors. Prospective cohort studies are essential for assessing other risk factors for cancer development in SjD patients.

Indexed as

LymphomaNeoplasmsSjogren's SyndromeAdultAgedBrazilBreast NeoplasmsFemaleHumansMaleMiddle AgedPrevalenceRegistriesRetrospective StudiesRisk FactorsThyroid NeoplasmsCancerLymphomaSjögren’s diseaseSjögren’s syndromeSolid neoplasia

Identifiers

PMID40836309
PMCPMC13488685

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