Zongyuan Li , Cheng Yu , Jianqi Hao , Yueli Shu , Jian Zhang , Kejia Zhao , Qiang Pu , Lunxu Liu
{"title":"Identifying environmental factors and biological metrics associated with cancer prevalence and mortality: An environment-wide association study","authors":"Zongyuan Li , Cheng Yu , Jianqi Hao , Yueli Shu , Jian Zhang , Kejia Zhao , Qiang Pu , Lunxu Liu","doi":"10.1016/j.canep.2025.102828","DOIUrl":"10.1016/j.canep.2025.102828","url":null,"abstract":"<div><h3>Background</h3><div>Present knowledge about determinants of oncogenesis and cancer mortality remains incomplete, inconsistent, and controversial. We aimed to conduct an environment-wide association study (EWAS) to systematically investigate and tentatively validate correlations of environmental factors and biological metrics with prevalence and mortality of cancer.</div></div><div><h3>Methods</h3><div>All eligible participants were selected from the US National Health and Nutrition Examination Survey (NHANES) and randomly split into training and testing sets by survey years. Environmental and biological exposures were assessed through either physical examinations or laboratory tests. We conducted survey-weighted logistic regression and COX proportional hazards regression models to investigate the relationships of 398 factors with cancer prevalence and 380 factors with cancer mortality, respectively. To adjust for multiple comparisons, positive findings in the training set (false discovery rate [FDR] < 5 %) were tentatively validated in the testing set (P value < 0.05). Random forest models were further fitted to evaluate the importance and diagnostic value of identified factors in relation to cancer prevalence.</div></div><div><h3>Results</h3><div>Overall, 55,021 general participants and 5163 cancer survivors were included in the study of cancer prevalence and mortality, respectively. After adjusting potential confounders, we identified 7 environmental or biological factors (e.g. total bilirubin, testosterone, and beta-cryptoxanthin) associated with cancer prevalence in the general population, as well as 21, 8, and 6 indicators associated with all-cause (e.g. C-reactive protein), cancer-specific (e.g. blood selenium), and noncancer mortality (e.g. albumin) among individuals with cancer, respectively. EWAS-identified factors contributed to better performance of random forest models in predicting cancer prevalence.</div></div><div><h3>Conclusions</h3><div>Employing an EWAS approach, this study provided novel insights into potential targets for prevention and control of cancer.</div></div>","PeriodicalId":56322,"journal":{"name":"Cancer Epidemiology","volume":"97 ","pages":"Article 102828"},"PeriodicalIF":2.4,"publicationDate":"2025-04-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143856048","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Rochelle Woudberg , Sarah Muriel Meiring , Edina Sinanovic
{"title":"Leukemia epidemiology and burden of disease in South Africa: 2015–2019","authors":"Rochelle Woudberg , Sarah Muriel Meiring , Edina Sinanovic","doi":"10.1016/j.canep.2025.102818","DOIUrl":"10.1016/j.canep.2025.102818","url":null,"abstract":"<div><h3>Background</h3><div>Leukemia ranks as the 11th most prevalent cancer globally, contributing significantly to the cancer burden. Despite its rising impact, recent epidemiological data on leukemia in South Africa remain limited. This study investigates the incidence, mortality trends, and disease burden of leukemia in South Africa from 2015 to 2019.</div></div><div><h3>Methods</h3><div>Leukemia incidence data were obtained from the South African National Cancer Registry, and mortality data from Statistics South Africa for 2015–2019. Age-standardized incidence and mortality rates were calculated using mid-year population data and the Segi world standard population for standardization. The burden of disease was quantified using Years of Life Lost (YLLs), Years Lived with Disability (YLDs), and Disability-Adjusted Life Years (DALYs). Rates were compared by age, sex, year, and province.</div></div><div><h3>Results</h3><div>There were 2 001 new cases of leukemia and 1 244 deaths reported, with an incidence rate of 4.11 per 100,000 and mortality rate of 3.01 per 100,000 population. The male-to-female ratio was 1.1:1 and the mean age was 38 years at diagnosis and 53 at death. Acute myeloid leukemia was the most common type of leukemia in South Africa. Gauteng had the highest age standardized incidence rate (4.92 per 100,000), and the Western Cape had the highest age standardized mortality rate (3.98 per 100,000). In 2019, leukemia accounted for 6 309 DALYs, with a decline in age standardized DALY (-1.04 %) and YLL (-4.7 %) rate, respectively.</div></div><div><h3>Conclusion</h3><div>This study provides up-to-date incidence and mortality data, expressing the burden of leukemia in South Africa. The age-standardized mortality and DALY rates showed favorable patterns over the study period. However, the incidence rates showed an increase, which may reflect the progressive aging and growth of the population. These findings highlight the need for sustained efforts to improve leukemia detection, treatment access, and healthcare quality in South Africa.</div></div>","PeriodicalId":56322,"journal":{"name":"Cancer Epidemiology","volume":"97 ","pages":"Article 102818"},"PeriodicalIF":2.4,"publicationDate":"2025-04-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143851433","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"HPV-unrelated oropharyngeal cancer has elevated risk of synchronous hepatobiliary second primary malignancies compared to HPV-related oropharyngeal cancer: a population-based study from SEER","authors":"Shaopan Cao , Mehran Asad Ayoubi","doi":"10.1016/j.canep.2025.102826","DOIUrl":"10.1016/j.canep.2025.102826","url":null,"abstract":"<div><h3>Background</h3><div>Our aim was to compare risk of synchronous and metachronous hepatobiliary second primary malignancies (SPMs) in survivors of human papillomavirus (HPV)-related [i.e., p16(+)] and HPV-unrelated [i.e., p16(-)] oropharyngeal cancer (OPC).</div></div><div><h3>Methods</h3><div>A retrospective study was conducted for cases with OPC diagnosis during years 2018–2021 who had known p16 status using data of USA from Surveillance, Epidemiology, and End Results (SEER) Program [Incidence - SEER Research Limited-Field Data, 22 Registries (excl IL and MA), Nov 2023 Sub (2000–2021)]. In the statistical analyses, death was considered as a competing event for the development of a hepatobiliary SPM. Bias due to unbalanced baseline characteristics was eliminated by adjustments using propensity score and inverse probability of treatment weighting (IPTW). Risk of development of a hepatobiliary SPM was assessed using propensity-score-adjusted time-varying Cox proportional hazard regression [adjusted hazard ratio (aHR) with 95 % confidence interval (95 % CI)].</div></div><div><h3>Results</h3><div>Overall, 25759 cases with tumor status of p16(-) (6353) and p16(+) (19406) with median (interquartile range) follow-up times of 14 (6, 26) and 20 (9, 32) months, respectively, were included. From these, 48 had a hepatobiliary SPM. Compared to HPV-related OPC, HPV-unrelated OPC had significantly elevated risk of synchronous all hepatobiliary SPMs [aHR= 2.39 (95 % CI, 1.11–5.15); P = 0.026] and synchronous hepatocellular carcinoma (HCC) SPM [aHR= 2.86 (95 % CI, 1.18–6.92); P = 0.020], but not metachronous ones. Curves of cumulative incidence of a hepatobiliary (or HCC) SPM and cumulative survival probability for those with a hepatobiliary SPM, both stratified by p16 status and adjusted by IPTW, were generated. The median survival time among patients with a hepatobiliary SPM was shorter for HPV-unrelated OPC (0.8 years) compared to HPV-related OPC (2.6 years).</div></div><div><h3>Conclusion</h3><div>The observed elevated risk was likely due to heavy alcohol and tobacco use and the protective role of HPV infection against HCC development in carriers of hepatitis C virus.</div></div>","PeriodicalId":56322,"journal":{"name":"Cancer Epidemiology","volume":"97 ","pages":"Article 102826"},"PeriodicalIF":2.4,"publicationDate":"2025-04-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143844380","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Julia Allas , Piret Veerus , Aleksei Baburin , Kaire Innos
{"title":"Correcting uterine cancer mortality in Estonia using linkage of causes of death and cancer registry data, 2000–2021","authors":"Julia Allas , Piret Veerus , Aleksei Baburin , Kaire Innos","doi":"10.1016/j.canep.2025.102823","DOIUrl":"10.1016/j.canep.2025.102823","url":null,"abstract":"<div><h3>Background</h3><div>Cervical and corpus uteri cancer mortality may be underestimated due to a proportion of deaths attributed to unspecified uterine cancer. The aim was to estimate corrected mortality rates and trends for cervical and corpus uteri cancer in Estonia after reallocation of underlying cause of death using individual linkage of death records and cancer registry records.</div></div><div><h3>Methods</h3><div>Deaths in Estonian female population in 2000–2021 with the underlying cause of cervical cancer (ICD-10 code C53), corpus uteri cancer (C54) or cancer of uterus not otherwise specified (C55) were individually linked to Estonian Cancer Registry to identify any cancers diagnosed in these persons. Underlying cause of death was reallocated if applicable. Original and corrected age-standardized (world) mortality trends were modelled using joinpoint regression.</div></div><div><h3>Results</h3><div>During 2000–2021, the corrected number of deaths was 1409 cervical cancer deaths (originally 1388, 1.5 % increase), 1146 corpus uteri cancer deaths (902, 27 % increase), and 50 unspecified uterine cancer deaths (368, 86 % decrease). Proportion of unspecified deaths decreased from 26 % (2000–2004) to 4 % (2016–2021) (p < 0.001). After correction, cervical cancer mortality trend steepened slightly from 0.8 % decrease per year to 1.1 % decrease (both significant). Corpus uteri cancer mortality trend changed direction from significant increase of 1.9 % per year to significant decrease of 1.4 % per year.</div></div><div><h3>Conclusions</h3><div>Routine linkage of causes of death records with cancer registry is warranted for validating underlying cause of death. The results emphasize the importance of the availability of medical documentation for physicians assigning cause of death as well as relevant training.</div></div>","PeriodicalId":56322,"journal":{"name":"Cancer Epidemiology","volume":"97 ","pages":"Article 102823"},"PeriodicalIF":2.4,"publicationDate":"2025-04-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143844554","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Soyoung Park , Yeon-Soon Ahn , Jungyun Lim , Sol Yu , Younghee Kim , Jongin Lee
{"title":"Association between humidifier disinfectant use and development of lung cancer: A nested case-cohort study","authors":"Soyoung Park , Yeon-Soon Ahn , Jungyun Lim , Sol Yu , Younghee Kim , Jongin Lee","doi":"10.1016/j.canep.2025.102822","DOIUrl":"10.1016/j.canep.2025.102822","url":null,"abstract":"<div><h3>Objective</h3><div>The outbreak of lung disease among humidifier disinfectants (HDs) users lead to the identification of humidifier disinfectants-associated lung injury (HDLI) cases. Subsequent research highlighted the respiratory health risks associated HDs but the connection to lung cancer remained uncertain. To assess the risk of lung cancer development among individuals exposed to HDs and to investigate the characteristics of HDs exposure influencing the occurrence of lung cancer.</div></div><div><h3>Materials and methods</h3><div>A cohort study was conducted using the national database, encompassing 7343 claimants exposed to HDs. The study focused on 195 confirmed lung cancer cases, employing the standardized incidence ratio (SIR) for comparisons with the general population, and the odds ratio (OR) using propensity score matching for internal comparisons.</div></div><div><h3>Results</h3><div>The study found a significantly higher incidence of lung cancer among individuals exposed to HDs compared to the general Korean population, with elevated SIRs observed in both men and women (SIR = 3.43, 95 % CI = 2.81–4.13 for men; SIR = 11.19, 95 % CI = 8.95–13.82 for women). In the propensity score-matched case-control design, a longer duration of HDs use was associated with an increased risk of lung cancer (OR = 2.48, 95 % CI = 1.35–4.56 for using HDs for more than 49 months and OR = 1.02, 95 % CI = 1.01 – 1.03 for every one month).</div></div><div><h3>Conclusion</h3><div>The findings suggest a potential association between HDs exposure and an increased risk of lung cancer.</div></div>","PeriodicalId":56322,"journal":{"name":"Cancer Epidemiology","volume":"97 ","pages":"Article 102822"},"PeriodicalIF":2.4,"publicationDate":"2025-04-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143844539","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Christine Ann Pittman Ballard , Yubo Wang , Carol Kruchko , Jill S. Barnholtz-Sloan , Yunqian Li , Quinn T. Ostrom
{"title":"Characteristics of long-term glioblastoma survivors diagnosed from 2010 to 2016 in the United States","authors":"Christine Ann Pittman Ballard , Yubo Wang , Carol Kruchko , Jill S. Barnholtz-Sloan , Yunqian Li , Quinn T. Ostrom","doi":"10.1016/j.canep.2025.102810","DOIUrl":"10.1016/j.canep.2025.102810","url":null,"abstract":"<div><h3>Background</h3><div>Glioblastoma (GBM) is the most common malignant primary central nervous system (CNS) tumor, accounting for half (50.9 %) of all malignant tumors diagnosed in the US. We conducted a population-based analysis using Centers for Disease Control and Prevention’s (CDC) National Program of Cancer Registries (NPCR) survival database investigate which patient- and tumor-level factors are characteristic of long-term survivors (LTS) of GBM.</div></div><div><h3>Methods</h3><div>Individual-level survival data containing diagnoses of primary GBM were obtained from the NPCR survival database for cases diagnosed during the period of January 1st, 2010 to December 31st, 2016, and followed through December 31st, 2019. Differences in LTS (>36-months) were investigated using χ<sup>2</sup> tests and multivariable logistic regression. Frequency of IDHmut-GBM by age was estimated in the same dataset from 2018 to 2021.</div></div><div><h3>Results</h3><div>Of the included GBM, 11.6 % met criteria for LTS. After adjustment for known prognostic factors, males (OR=0.78, p < 0.001) and age > 60 at diagnosis, were all significantly associated with decreased odds of LTS (70–79 years O =0.48, 80 + years OR=0<sub>.</sub>21, both p < 0.001). Frequency of IDHmut-GBM peaked from 25 to 34, with < 5 % of GBM in those > 50 having IDHmut-GBM. In a sensitivity analysis in those > 50 diagnosis, both male sex and age remained significant predictors of LTS</div></div><div><h3>Conclusion</h3><div>There are multiple patient- and tumor-level factors that are associated with improved survival in GBM, with the strongest effect sizes in the multivariable models being due to age. These results demonstrate substantial heterogeneity in GBM prognosis and emphasize the distinct survival advantage associated with age at diagnosis.</div></div>","PeriodicalId":56322,"journal":{"name":"Cancer Epidemiology","volume":"97 ","pages":"Article 102810"},"PeriodicalIF":2.4,"publicationDate":"2025-04-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143844452","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Kevin L’Espérance , Sreenath Madathil , Jennifer A. Ritonja , Michal Abrahamowicz , Vikki Ho , Belinda Nicolau , Jennifer O’Loughlin , Anita Koushik
{"title":"Trajectories of body fatness in adulthood and the risk of ovarian cancer","authors":"Kevin L’Espérance , Sreenath Madathil , Jennifer A. Ritonja , Michal Abrahamowicz , Vikki Ho , Belinda Nicolau , Jennifer O’Loughlin , Anita Koushik","doi":"10.1016/j.canep.2025.102814","DOIUrl":"10.1016/j.canep.2025.102814","url":null,"abstract":"<div><h3>Background</h3><div>While excess body fatness in older adulthood has been linked to ovarian cancer, the influence of changes in body fatness over time is unclear. This study examined the association between adulthood trajectories of body mass index (BMI), a proxy for body fatness, and ovarian cancer.</div></div><div><h3>Methods</h3><div>In a population-based case-control study (440 cases, 820 controls), we used a group-based trajectory approach to identify BMI trajectories from age 20–70. Using unconditional logistic regression, we estimated adjusted odds ratios (aOR) and 95 % confidence intervals (95 % CI) for the associations between the estimated trajectories and ovarian cancer.</div></div><div><h3>Results</h3><div>We identified three distinct BMI trajectories: a normal-stable trajectory, a normal-to-overweight trajectory and an overweight-to-obese trajectory, which included 63.2 %, 31.0 % and 6.8 % of the population, respectively. Multivariable aORs suggested that participants with normal weight at the onset of adulthood who became overweight over their adulthood time did not differ in their risk of ovarian cancer compared to those who maintained a normal weight throughout adulthood (aOR (95 %CI): 0.89 (0.69–1.16)). Among those in the overweight-to-obese trajectory, the aOR (95 %CI) was 1.45 (0.87–2.43), and thus in the direction of an increased ovarian cancer risk compared to those who maintained a normal weight.</div></div><div><h3>Conclusion</h3><div>Our findings underscore the need for further research to clarify the role of body fatness across the lifetime in the etiology of ovarian cancer.</div></div>","PeriodicalId":56322,"journal":{"name":"Cancer Epidemiology","volume":"96 ","pages":"Article 102814"},"PeriodicalIF":2.4,"publicationDate":"2025-04-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143834758","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Lucia Cayuela , Anna Michela Gaeta , Victoria Achaval Rodríguez , Anna Annunziata , Giuseppe Fiorentino , Aurelio Cayuela
{"title":"Declining early-onset lung cancer mortality in Spain: Sex-specific trends and regional variations, 1999–2022","authors":"Lucia Cayuela , Anna Michela Gaeta , Victoria Achaval Rodríguez , Anna Annunziata , Giuseppe Fiorentino , Aurelio Cayuela","doi":"10.1016/j.canep.2025.102816","DOIUrl":"10.1016/j.canep.2025.102816","url":null,"abstract":"<div><h3>Background</h3><div>Lung cancer (LC) is the leading cause of cancer mortality globally, with a concerning increase in early-onset lung cancer (EO-LC), defined as cases diagnosed before age 50. This study investigates EO-LC mortality trends in Spain from 1999 to 2022, focusing on regional and gender disparities.</div></div><div><h3>Methods</h3><div>Data on LC mortality were obtained from the Spanish National Institute of Statistics, employing International Classification of Diseases codes for analysis. Joinpoint regression was utilized to estimate age-standardized mortality rates (ASMRs) and identify significant mortality trends across different Autonomous Communities (ACs).</div></div><div><h3>Results</h3><div>Total LC deaths in Spain increased; however, the proportion of EO-LC deaths significantly declined. In men, the proportion of EO-LC deaths decreased from 6.2 % to 1.6 %, while in women, it fell from 11.6 % to 3.3 %. The ASMR for EO-LC in men decreased from 8.4 per 100,000 to 1.6 per 100,000 (average annual percentage change (AAPC): −6.7 %). In women, ASMR rates fell from 1.7 per 100,000 to 1.2 per 100,000 (AAPC: −2.1 %). Notable regional declines were observed, particularly in Castile & León (-8.6 %) and Madrid (-8.2 %) for men. In contrast, female mortality trends were heterogeneous, with some regions exhibiting stable rates and others showing initial increases followed by significant declines.</div></div><div><h3>Conclusions</h3><div>While our findings indicate an overall improvement in EO-LC mortality rates—particularly among men—they also reveal ongoing regional and gender disparities that require targeted intervention. The strengths and limitations of this study emphasize the need for continued surveillance and further investigations into the determinants of EO-LC mortality.</div></div>","PeriodicalId":56322,"journal":{"name":"Cancer Epidemiology","volume":"97 ","pages":"Article 102816"},"PeriodicalIF":2.4,"publicationDate":"2025-04-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143820288","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Hamin Lee , Jin-Wu Nam , Mi Kyung Kim , Inah Kim , Yu-Mi Kim , Boyoung Park
{"title":"Validation of self-reported cancer diagnoses in the Korean Atomic Bomb Survivor Cohort study","authors":"Hamin Lee , Jin-Wu Nam , Mi Kyung Kim , Inah Kim , Yu-Mi Kim , Boyoung Park","doi":"10.1016/j.canep.2025.102817","DOIUrl":"10.1016/j.canep.2025.102817","url":null,"abstract":"<div><h3>Background</h3><div>Owing to the short history of the National Cancer Registry, self-reported cancer history is an important source of morbidity in recently constructed cohorts or cohorts of the older population. This study aimed to evaluate the validity of the self–reported cancer history gathered through the Korean Atomic Bomb Survivor Cohort (K-ABC) study compared with the Korean Central Cancer Registry (KCCR).</div></div><div><h3>Methods</h3><div>Among the K-ABC participants recruited from 2020 to 2024, self-reported cancer history from 1756 participants was linked to the KCCR. The sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), and kappa coefficient were estimated for each cancer site.</div></div><div><h3>Results</h3><div>Among 181 participants with a minimum of one record in the KCCR, 164 reported a history of cancer. Overall cancers and each cancer site showed high sensitivity, PPV, and kappa values of > 80 %, > 66 %, and > 0.73, respectively, except for cervical and lung cancers, which showed sensitivities of < 50 % and kappa values of 0.33 and 0.59, respectively. High specificity and NPV (≥99 %) were observed for all cancer sites.</div></div><div><h3>Conclusions</h3><div>The validity of the self-reported cancer history of the K-ABC showed a relatively high level of agreement with the KCCR records. These findings indicate that self-reported cancer information from the K-ABC study is valid for all sexes and ages but needs consideration when used for evaluating cervical and lung cancer.</div></div>","PeriodicalId":56322,"journal":{"name":"Cancer Epidemiology","volume":"97 ","pages":"Article 102817"},"PeriodicalIF":2.4,"publicationDate":"2025-04-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143820289","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}