Evidence map›Paper›PMID 37807065›Full record

ArticleBMC cancer2023

Risks of non-ovarian cancers in women with borderline ovarian tumor: a national cohort study in Sweden.

Arturas Dobilas, Filip Jansåker, Xinjun Li, Kristina Sundquist, Christer Borgfeldt

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2023. 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
0.3field-weighted citation impact, top 33% 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

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. Article
  2. 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

5 authors at 2 institutions in 4 countries.

Arturas DobilasDepartment of Obstetrics and Gynaecology, Skåne University Hospital, Klinikgatan 12, Lund, 221 85, Sweden. arturas.dobilas@med.lu.se.ORCID https://orcid.org/0000-0001-6884-2640
Filip JansåkerCenter for Primary Health Care Research, Department of Clinical Sciences Malmö, Lund University, Lund, Sweden.ORCID https://orcid.org/0000-0003-0670-9996
Xinjun LiCenter for Primary Health Care Research, Department of Clinical Sciences Malmö, Lund University, Lund, Sweden.ORCID https://orcid.org/0000-0002-5559-4657
Kristina SundquistCenter for Primary Health Care Research, Department of Clinical Sciences Malmö, Lund University, Lund, Sweden.ORCID https://orcid.org/0000-0001-8031-279X
Christer BorgfeldtDepartment of Obstetrics and Gynaecology, Skåne University Hospital, Klinikgatan 12, Lund, 221 85, Sweden.ORCID https://orcid.org/0000-0003-2267-8325
Lund University · SEShimane University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAssociations between different cancer types are known. The affirmation of the risk for non-ovarian cancer after ovarian borderline tumors (BOT) is, however, sparse.

aimTo analyze the risk of subsequent or simultaneous cancers in women with BOTs compared with the general female Swedish population.

methodsAn open cohort study (1995-2018) was conducted where a diagnosis of BOTs as well as subsequent or simultaneous cancer diagnoses were obtained from the Swedish Cancer Register and matched to the Total Population Register. Each woman with BOT was followed until non-ovarian cancer, death or emigration and could only be included once for the outcome. Standardized incidence ratios (SIRs) with 95% confidence intervals (CIs) for specific non-ovarian cancers were analyzed.

resultsThe 4998 women with serous and mucinous BOTs were diagnosed during 1995-2018 with a mean age of 55.7 years (SD 16.0) at diagnosis. Compared with the general female population, women with BOTs had increased risks for non-ovarian cancer in colon (SIR = 2.5; 95% CI 2.0-3.1), rectum (SIR = 1.7; 95% CI 1.1-2.5), small intestine (SIR = 5.0; 95% CI 2.3-9.5), cervix (SIR = 2.5; 95% CI 1.4-4.2), endometrium (SIR = 2.4; 95% CI 1.9-3.1), pancreas (SIR = 2.3; 95% CI 1.4-3.5), upper aerodigestive tract (SIR = 2.2; 95% CI 1.2-3.8), lung (SIR = 1.8; 95% CI 1.4-2.3), kidney (SIR = 2.3; 95% CI 1.4-3.7) and bladder (SIR = 1.8; 95% CI 1.1-2.8). Among women with serous BOTs, the risk of thyroid gland cancer (SIR = 3.1; 95% CI 1.2-6.4) was also increased. Lung and pancreas cancer showed increased risks more than 1 year after a diagnosis of BOT.

conclusionsThis Swedish population-based study demonstrated an increased risk of multiple malignancies including lung and pancreatic cancers beyond the first year of diagnosis in patients with borderline ovarian tumors (BOTs), suggesting a potential shared etiology.

Indexed as

Ovarian NeoplasmsCohort StudiesFemaleHumansIncidenceMiddle AgedRisk FactorsSwedenBorderline ovarian tumorsCancer riskCohort studyNationwideStandardized incidence ratios

Identifiers

PMID37807065
PMCPMC10561436
OpenAlexW4387440123

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.