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Statin and Immune-Related Cardiovascular Events in Lung Cancer Patients Receiving Immune Checkpoint Inhibitors.

Oncology 2026 Vol.104(3) p. 319-326

Song J, Chi KY, Jeon H, Chang YC, Xanthavanij N, Tang Z, Chang Y, Chiang CH, Lin YS, Lin S, Xu XH, Chiang CH

📝 환자 설명용 한 줄

[INTRODUCTION] Immune checkpoint inhibitors (ICIs) have improved lung cancer treatment but are associated with an increased risk of cardiotoxicity.

🔬 핵심 임상 통계 (초록에서 자동 추출 — 원문 검증 권장)
  • 95% CI 0.78-0.98
  • HR 0.87
  • 추적기간 12 months
  • 연구 설계 cohort study

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BibTeX ↓ RIS ↓
APA Song J, Chi KY, et al. (2026). Statin and Immune-Related Cardiovascular Events in Lung Cancer Patients Receiving Immune Checkpoint Inhibitors.. Oncology, 104(3), 319-326. https://doi.org/10.1159/000546204
MLA Song J, et al.. "Statin and Immune-Related Cardiovascular Events in Lung Cancer Patients Receiving Immune Checkpoint Inhibitors.." Oncology, vol. 104, no. 3, 2026, pp. 319-326.
PMID 40398400
DOI 10.1159/000546204

Abstract

[INTRODUCTION] Immune checkpoint inhibitors (ICIs) have improved lung cancer treatment but are associated with an increased risk of cardiotoxicity. We investigated whether statins could mitigate ICI-associated cardiovascular risks in lung cancer patients.

[METHODS] We performed a retrospective, propensity score-matched cohort study utilizing the TriNetX database. We identified lung cancer patients receiving ICIs between April 2013 and June 2023. We created two cohorts: statin users and non-users. The primary efficacy outcome was major adverse cardiovascular events (MACE), defined as a composite of myocardial infarction, ischemic stroke, and heart failure. The secondary efficacy outcomes were myocarditis and cardiac arrest. Safety outcomes were all-cause mortality and serious immune-related adverse events (irAEs).

[RESULTS] A total of 16,650 lung cancer patients undergoing ICIs were identified, consisting of 6,812 statin users and 9,838 non-users. After propensity score matching, 4,379 patients were well-matched in baseline characteristics. Over a follow-up period of 12 months, statin use was associated with a lower risk of MACE (HR: 0.87, 95% CI: 0.78-0.98), primarily driven by reductions in myocardial infarction (HR: 0.75, 95% CI: 0.58-0.97) and heart failure (HR: 0.85, 95% CI: 0.74-0.98). For safety outcomes, statin use was associated with a reduction in all-cause mortality (HR: 0.83, 95% CI: 0.77-0.90) and did not result in an increased risk of serious irAEs.

[CONCLUSION] The use of statins in lung cancer patients with cardiovascular risk factors and without previous cardiovascular events undergoing immunotherapy was associated with a reduction in MACE and all-cause mortality without an increased risk of serious adverse events.

MeSH Terms

Humans; Hydroxymethylglutaryl-CoA Reductase Inhibitors; Male; Female; Lung Neoplasms; Immune Checkpoint Inhibitors; Aged; Retrospective Studies; Middle Aged; Cardiovascular Diseases; Propensity Score; Cardiotoxicity

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