Abstract 459P
Background
With cancer as the leading cause of death in Korea and globally, addressing non-cancer mortality, specifically cardiovascular disease, is critical. Dyslipidemia, a significant risk factor for cardiovascular disease, requires proper management in cancer survivors. This study aims to analyze factors associated with undertreatment of dyslipidemia in cancer survivors and investigate the impact of the National Health Screening Program (NHSP) on undertreatment in Korea.
Methods
This cross-sectional study analyzed data from the Korea National Health and Nutrition Survey (KNHANES) conducted between 2007 and 2019. It included 2,226 participants (792 males, 1,434 females) aged 40-75 who had a history of cancer. Self-reported questionnaires collected information following the 2018 Cholesterol Treatment Guidelines by the American College of Cardiology/American Heart Association. Multiple logistic regression analysis with integrated weights was performed.
Results
Among cancer survivors, 16.3% received treatment for dyslipidemia. Of those who were untreated, 46.64% had normal blood lipid levels, while 37.0% were not receiving adequate treatment. Additionally, 72.7% of cancer survivors participated in the NHSP, and the undertreatment rate for dyslipidemia was significantly lower in the screened group compared to the non-screened group (34.14% vs. 44.78%; P < 0.001). Adjusting for age and sex, cancer survivors in the non-screened group had a significantly higher risk of not receiving appropriate dyslipidemia treatment (odds ratio [OR] 1.47, 95% confidence interval [CI] 1.10, 1.97). Even after considering socioeconomic and cancer-related factors, the non-screened group remained significantly associated with undertreatment of dyslipidemia (OR 1.36, 95% CI: 1.02, 1.82), especially among female cancer survivors (OR 1.49, 95% CI: 1.05, 2.14).
Conclusions
This study is the first to assess the association between NHSP and undertreatment of dyslipidemia. Encouraging cancer survivors to participate in the NHSP would be an effective strategy to reduce the incidence and mortality of concurrent cardiovascular disease, ultimately improving the overall health of cancer survivors.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The author.
Funding
Has not received any funding.
Disclosure
The author has declared no conflicts of interest.
Resources from the same session
561P - Mechanisms of osimertinib resistance using circulating tumor DNA analyses for EGFR-mutated non-small cell lung cancer, results from ELUCIDATOR: A prospective observational multicenter study
Presenter: Daijiro Harada
Session: Poster Display
Resources:
Abstract
562P - First-line (1L) osimertinib (osi) ± platinum-pemetrexed in patients (pts) with EGFRm advanced NSCLC: FLAURA2 China cohort
Presenter: Yan Yu
Session: Poster Display
Resources:
Abstract
563P - Real-world effectiveness and safety of first-line osimertinib for EGFR-mutated advanced NSCLC in China (FLOURISH study)
Presenter: Jianya Zhou
Session: Poster Display
Resources:
Abstract
564P - Co-occurring EGFR p.E709X mutation affects the treatment response to the third-generation EGFR-TKIs in EGFR p.G719X-mutant patients with advanced NSCLC
Presenter: Wen Feng Fang
Session: Poster Display
Resources:
Abstract
565P - Genome-guided targeted therapy combination improves survival in patients with advanced EGFR mutation positive NSCLC failing osimertinib
Presenter: Molly Li
Session: Poster Display
Resources:
Abstract
566P - Safety of tepotinib + osimertinib in EGFR-mutant NSCLC with MET amplification after first-line osimertinib
Presenter: Chong Kin Liam
Session: Poster Display
Resources:
Abstract
567P - Furmonertinib in combination with bevacizumab and intrathecal chemotherapy as later-line re-challenge treatment in EGFR –mutated NSCLC patients with leptomeningeal metastasis after third-generation EGFR-TKIs treatment failure
Presenter: Fang Cun
Session: Poster Display
Resources:
Abstract
568P - First-line (1L) osimertinib + platinum-pemetrexed in EGFR-mutated (EGFRm) advanced NSCLC: Updated FLAURA2 safety run-in (SRI) results
Presenter: David Planchard
Session: Poster Display
Resources:
Abstract
569P - Whole-transcriptome sequencing of transformed small-cell lung cancer from EGFR-mutated lung adenocarcinoma reveals LUAD–like and SCLC–like subsets
Presenter: Chan-Yuan Zhang
Session: Poster Display
Resources:
Abstract
570P - First-line osimertinib for patients with advanced NSCLC harboring EGFR mutations: A real-world study
Presenter: Wenxiang Ji
Session: Poster Display
Resources:
Abstract