Evidence map›Paper›PMID 41049581›Full record

ArticleTherapeutic advances in medical oncology2025

Temporal trends in treatment-related cardiopulmonary disease-specific mortality in NSCLC based on pathological subtypes: a retrospective population-based cohort study.

You Mo, Xinyi Liang, Duncan Wei, Dawei Chen, Jinming Yu

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Article in Therapeutic advances in medical oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

You MoThe First Affiliated Hospital of Shantou University Medical College, Shantou, Guangdong, China.ORCID https://orcid.org/0000-0001-5283-0741
Xinyi LiangShandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, Shandong, China.ORCID https://orcid.org/0009-0004-6610-1207
Duncan WeiThe First Affiliated Hospital of Shantou University Medical College, Shantou, Guangdong, China.
Dawei ChenDepartment of Shandong Provincial Key Laboratory of Precision Oncology, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, No. 440, Jiyan Road, Huaiyin District, Jinan, Shandong 250000, China.ORCID https://orcid.org/0000-0002-6762-7997
Jinming YuThe First Affiliated Hospital of Shantou University Medical College, Shantou, Guangdong, China.ORCID https://orcid.org/0000-0001-5933-9912

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: While cancer-specific mortality has decreased with therapeutic advances, a growing proportion of survivors are at risk of treatment-related adverse effects (AEs). Objectives: To assess cardiopulmonary disease-specific mortality risks in patients with non-small-cell lung cancer (NSCLC) based on pathological subtypes. Design: This was a retrospective cohort study. Mortality data from the Surveillance, Epidemiology, and End Results Program database and AE data from the FDA Adverse Event Reporting System were analyzed in NSCLC patients. In addition, an independent validation cohort comprising 161 NSCLC patients was enrolled. Methods: The piecewise regression was established using the Joinpoint software to characterize temporal trends. Univariate and multivariate analyses for specific mortality were performed using the Cox risk regression model. Results: From 2012 to 2016, patients with lung adenocarcinoma (LADC) showed a 2.06% annual reduction in mortality. Conversely, this population exhibited a 3.82% yearly increase in cardiovascular disease (CVD)-specific mortality and a 6.54% rise in pulmonary disease-specific mortality during the same period. Patients with lung squamous cell carcinoma (LSCC) may have benefited more from the initiation of immunotherapy, with a gradual decrease in incidence (2016-2019, -5.19%). The incidence of large-cell lung cancer (LCLC) declined significantly (2008-2012, -14.52%; 2012-2016, -7.93%; 2016-2019, -6.42%), with decrease in overall mortality (2008-2012, -10.63%; 2012-2016, -8.76%; 2016-2019, -10.27%) and cancer-specific mortality (2008-2012, -12.17%; 2012-2016, -10.35%; 2016-2019, -10.78%). LCLC showed no significant rise in CVD-specific mortality (2012-2016: CVD-specific mortality, -4.83%; pulmonary disease-specific mortality, -0.82%. 2016-2019: CVD-specific mortality, -21.82%; pulmonary disease-specific mortality, -12.78%) compared to LSCC and LADC. The reporting odds ratio (ROR = 47.80, 95% CI, 24.44-93.50) of endocarditis of LADC was the top-reported AE. Multivariate analysis showed that immune checkpoint blockade was associated with increased CVD death (HR = 4.602, 95% CI, 1.154-18.359, Conclusion: Our analyses revealed a temporal increase in cardiopulmonary disease-specific mortality among NSCLC patients during the study period. This trend coincided with the introduction of targeted therapies and immunotherapies, particularly in LADC patients. CVD-specific mortality risk requires extensive attention during anticancer therapy, regardless of the geographical population.

Indexed as

cardiovascular diseaseimmunotherapylung cancertargeted therapy

Identifiers

PMID41049581
PMCPMC12491816

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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.