# Acetaminophen is associated with improved survival in critically ill lung cancer patients: A propensity score-matched cohort study

**Authors:** Chen Chen, Weijia Zeng, Yunyi Li, Zhihui Yang, Xue He

PMC · DOI: 10.7150/ijms.122435 · 2026-01-14

## TL;DR

Acetaminophen may improve survival in critically ill lung cancer patients, according to a study using hospital data.

## Contribution

This study is the first to show a survival benefit of acetaminophen in critically ill lung cancer patients using propensity score matching.

## Key findings

- Acetaminophen use was linked to a 22.0% 28-day mortality rate versus 37.5% in non-users.
- Propensity score analysis showed acetaminophen reduced mortality risks across multiple timeframes.
- Patients aged ≥65 and those with higher SOFA scores showed notable survival benefits.

## Abstract

Background: Acetaminophen is widely used in intensive care units, yet its impact on mortality among critically ill patients with primary lung cancer remains unclear. Given the high disease burden and potential immunomodulatory effects of acetaminophen, robust evidence is needed to clarify its prognostic relevance in this population.

Methods: We conducted a retrospective cohort study using the MIMIC-IV v2.2 database, including 1,127 critically ill patients with primary lung cancer. Baseline variables comprised demographics, comorbidities, illness severity scores (SOFA, APSIII, SAPSII, OASIS), and laboratory parameters. To minimize confounding, propensity score matching was applied.

Results: A total of 1,127 critically ill patients with primary lung cancer were included, of whom 403 received acetaminophen. The 28-day mortality rate was 22.0% in the acetaminophen group compared to 37.5% in the non-acetaminophen group. After adjusting for baseline differences using inverse probability of treatment weighting (IPTW), acetaminophen exposure was associated with a significantly lower risk of 28-day mortality (HR=0.75, 95% CI: 0.60-0.93, p=0.015). In addition to 28-day mortality, acetaminophen use was consistently associated with reduced risks of ICU mortality, in-hospital mortality, 30-day mortality, 90-day mortality, and 365-day mortality. Subgroup analyses identified patients aged ≥65 years and those with a SOFA score ≥3 as particularly noteworthy subgroups.

Conclusion: Acetaminophen use was associated with significantly reduced short- and long-term mortality in critically ill patients with primary lung cancer. These findings suggest a potential survival benefit beyond its conventional symptomatic use and underscore the need for prospective studies to validate its therapeutic role in this high-risk population.

## Linked entities

- **Chemicals:** Acetaminophen (PubChem CID 1983)
- **Diseases:** lung cancer (MONDO:0005138)

## Full-text entities

- **Genes:** STAT3 (signal transducer and activator of transcription 3) [NCBI Gene 6774] {aka ADMIO, ADMIO1, APRF, HIES}
- **Diseases:** OASIS (MESH:D045169), diabetes (MESH:D003920), chronic pulmonary disease (MESH:D002908), Comorbidity (MESH:D004194), MIMIC (MESH:C000657744), congestive heart failure (MESH:D006333), delirium (MESH:D003693), liver disease (MESH:D008107), myocardial infarction (MESH:D009203), fever (MESH:D005334), ARDS (MESH:D012128), pain (MESH:D010146), inflammatory (MESH:D007249), APS (MESH:D000208), renal disease (MESH:D007674), peripheral vascular disease (MESH:D016491), infection (MESH:D007239), rhabdomyolysis (MESH:D012206), acute kidney injury (MESH:D058186), carcinoid tumors of the bronchus and lung (MESH:D002276), oncologic (MESH:D000072716), failure (MESH:D051437), cerebrovascular disease (MESH:D002561), paraplegia (MESH:D010264), sepsis (MESH:D018805), Organ Failure (MESH:D009102), cancer (MESH:D009369), Lung cancer (MESH:D008175), febrile (MESH:D000071072), critical illness (MESH:D016638)
- **Chemicals:** Oxygen (MESH:D010100), Acetaminophen (MESH:D000082), lipid (MESH:D008055), prostaglandin (MESH:D011453), ibuprofen (MESH:D007052), creatinine (MESH:D003404)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12825139/full.md

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Source: https://tomesphere.com/paper/PMC12825139