Sex specific familial risk in lung cancer through changing histologies in Sweden
Language English Country United States Media print-electronic
Document type Journal Article
Grant support
LX22NPO5102
The Cooperatio SURG and National Institute for Cancer Research-NICR
CZ.02.01.01/00/22_008/0004644
European Union-Next Generation EU and the SALVAGE Project
The Swedish Research Council, Jane and Aatos Erkko Foundation, Sigrid Juselius Foundation, Finnish Cancer Organizations and Helsinki University Central Hospital
PubMed
40156379
PubMed Central
PMC12232509
DOI
10.1002/ijc.35431
Knihovny.cz E-resources
- Keywords
- adenocarcinoma, age of onset, incidence trend, proband, sibling risk,
- MeSH
- Adenocarcinoma epidemiology pathology MeSH
- Adult MeSH
- Genetic Predisposition to Disease MeSH
- Incidence MeSH
- Middle Aged MeSH
- Humans MeSH
- Lung Neoplasms * epidemiology pathology genetics MeSH
- Registries statistics & numerical data MeSH
- Risk Factors MeSH
- Aged MeSH
- Sex Factors MeSH
- Carcinoma, Squamous Cell epidemiology pathology MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Geographicals
- Sweden epidemiology MeSH
Familial clustering of lung cancer (LC) is related to shared smoking habits but the contribution of other potential factors such as sex or histology is not well known, and these are the subjects of the present study in Sweden. Family relationships (from Multigeneration register) and diagnosed cancers (from Cancer registry) were obtained from the national registers from 1961 to 2021. The overall familial risk for LC was constant from the 1990s but the male familial risk decreased while the female familial risk doubled at the same time when female incidence doubled. The female familial risk for mother-daughter pairs was higher (SIR = 2.2 [2.0-2.3], N = 716) than for father-son pairs (SIR = 1.6 [1.5-1.8], N = 962). The histology-specific familial risks for adenocarcinoma, squamous cell carcinoma, small cell and large cell carcinoma were highest for concordant histology but also present for discordant histology. The number of family members diagnosed with LC was a strong determinant of familial risk. The novel results showed that familial risk of LC depends on the background incidence of LC and is higher for women compared to men. We demonstrated further an increased familial risk for each of the four histological types of LC which was higher for concordant than discordant histologies but was even detected between discordant histologies suggesting that LC histology is not a genetic trait.
Biomedical Center Faculty of Medicine Charles University Pilsen Pilsen Czech Republic
Center for Primary Health Care Research Lund University Malmö Sweden
Comprehensive Cancer Center Helsinki University Hospital Helsinki Finland
Division of Cancer Epidemiology German Cancer Research Center Heidelberg Germany
Division of Pediatric Neurooncology German Cancer Research Center Heidelberg Germany
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