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        <datestamp>2026-09-21T05:36:32Z</datestamp>
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          <dc:title>Table 1_Renin–angiotensin system inhibitor use and survival outcomes in lung cancer: a systematic review and meta-analysis.docx</dc:title>
          <dc:creator>Yongqian Liao (25080481)</dc:creator>
          <dc:creator>Jinhai Shen (1446184)</dc:creator>
          <dc:creator>Yonghe Liao (20681697)</dc:creator>
          <dc:creator>Yuxuan Lin (1370199)</dc:creator>
          <dc:creator>Nengyong Zeng (25080484)</dc:creator>
          <dc:subject>Pharmacology</dc:subject>
          <dc:subject>lung cancer</dc:subject>
          <dc:subject>meta-analysis</dc:subject>
          <dc:subject>overall survival</dc:subject>
          <dc:subject>progression-free survival</dc:subject>
          <dc:subject>renin-angiotensin system inhibitors</dc:subject>
          <dc:description>Background&lt;p&gt;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.&lt;/p&gt;Methods&lt;p&gt;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.&lt;/p&gt;Results&lt;p&gt;Twenty-six studies involving 403,423 patients were included. RASi use was associated with longer overall survival (OS; HR = 0.76, 95% CI: 0.70–0.83; I&lt;sup&gt;2&lt;/sup&gt; = 82.9%) and progression-free survival (PFS; HR = 0.79, 95% CI: 0.70–0.89; I&lt;sup&gt;2&lt;/sup&gt; = 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.&lt;/p&gt;Conclusion&lt;p&gt;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.&lt;/p&gt;Systematic Review Registration&lt;p&gt;https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD420251053671, identifier: CRD420251053671.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-21T05:36:32Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.3389/fphar.2026.1953204.s001</dc:identifier>
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          <dc:rights>CC BY 4.0</dc:rights>
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