Key result
Renin-angiotensin system inhibitor use was associated with improved overall survival (HR 0.76) in lung cancer patients in conventional meta-analysis, but this association was attenuated to the null (HR 1.00) after adjusting for small-study effects.
Why the study?
The association between renin-angiotensin system inhibitor use and survival outcomes in lung cancer remains uncertain.
Does renin-angiotensin system inhibitor (RASi) use improve overall survival and progression-free survival in patients with lung cancer?
Systematic Review (n=403,423)
Does renin-angiotensin system inhibitor (RASi) use improve overall survival and progression-free survival in patients with lung cancer?
Hazard Ratio: 0.76 (95% CI 0.7–0.83)
While conventional meta-analysis suggests RASi use is associated with improved survival in lung cancer patients, significant small-study effects and heterogeneity attenuate the overall survival benefit, indicating the need for cautious interpretation.
Caution against prescribing RASi for expected oncologic benefit in lung cancer; challenges prior meta-analyses by.
Background: Renin-angiotensin system inhibitors (RASi) have been associated with favorable survival outcomes across various cancers, but their association with survival in lung cancer remains uncertain. We conducted a systematic review and meta-analysis to evaluate the association between RASi use and survival outcomes in patients with lung cancer. Methods: PubMed and Embase were searched from inception to 6 July 2026. Pooled hazard ratios (HRs) with 95% confidence intervals (CIs) were calculated using random-effects models. Subgroup and sensitivity analyses, including large-study restricted analysis and precision-effect test and precision-effect estimate with standard error (PET-PEESE) regression, were performed to explore heterogeneity and assess the potential influence of small-study effects. Results: = 40.9%) in conventional random-effects meta-analyses. Subgroup analyses generally showed consistent associations across treatment modalities and geographic regions, although substantial heterogeneity remained in several subgroups. Egger's test indicated small-study effects for OS. Although the large-study restricted analysis remained significant (HR = 0.82, 95% CI: 0.74-0.90), PET-PEESE adjustment attenuated the estimate to the null (HR = 1.00, 95% CI: 0.95-1.05). No significant evidence of small-study effects was observed for PFS. Conclusion: Conventional meta-analysis showed an association between RASi use and longer OS and PFS. However, the OS association was attenuated to the null after adjustment for small-study effects, indicating that the magnitude and robustness of the observed OS association remain uncertain. These findings should therefore be interpreted cautiously and require confirmation in well-designed prospective studies. Systematic Review Registration: https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD420251053671, identifier: CRD420251053671.
No takes yet. Share an insight, caveat, or question.
Liao et al. (2026) conducted a systematic review in Lung cancer (n=403,423). Renin-angiotensin system inhibitors (RASi) vs. Non-use of RASi was evaluated on Overall survival (HR 0.76, 95% CI 0.70-0.83). Renin-angiotensin system inhibitor use was associated with improved overall survival (HR 0.76) in lung cancer patients in conventional meta-analysis, but this association was attenuated to the null (HR 1.00) after adjusting for small-study effects.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: