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        <identifier>oai:figshare.com:article/33993130</identifier>
        <datestamp>2026-09-25T05:33:45Z</datestamp>
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          <dc:title>Supplementary file 1_Impact of immune checkpoint inhibitors as neoadjuvant/perioperative therapy for locally advanced resectable gastric/gastroesophageal junction adenocarcinoma: a systematic review and meta-analysis.pdf</dc:title>
          <dc:creator>Zhengyi Chen (4386883)</dc:creator>
          <dc:creator>Xin Liu (43569)</dc:creator>
          <dc:creator>Hanling Sun (25107736)</dc:creator>
          <dc:creator>Nini Cao (9394415)</dc:creator>
          <dc:creator>Junlin Zhou (5159339)</dc:creator>
          <dc:creator>Zihan Chen (1765921)</dc:creator>
          <dc:creator>Yang Song (88132)</dc:creator>
          <dc:creator>Jun Yao (9646)</dc:creator>
          <dc:subject>Genetic Immunology</dc:subject>
          <dc:subject>gastric/gastroesophageal junction adenocarcinoma</dc:subject>
          <dc:subject>immune checkpoint inhibitors</dc:subject>
          <dc:subject>meta-analysis</dc:subject>
          <dc:subject>neoadjuvant</dc:subject>
          <dc:subject>perioperative</dc:subject>
          <dc:subject>systematic review</dc:subject>
          <dc:description>Background&lt;p&gt;Immune checkpoint inhibitor (ICI)-based neoadjuvant/perioperative strategies are expanding for locally advanced resectable gastric/gastroesophageal junction (G/GEJ) adenocarcinoma, but the evidence base differs substantially across strategies, and improved pathological response has not consistently translated into survival benefit. We aimed to synthesize strategy-specific comparative and prospective single-arm evidence.&lt;/p&gt;Methods&lt;p&gt;PubMed, Web of Science, Embase, the Cochrane Library, and major oncology conference proceedings were searched from inception to August 3, 2026. RCTs and prospective single-arm trials evaluating ICI-containing treatment initiated before surgery were included. Five strategies were evaluated: ICI plus chemotherapy (ICI+CT), ICI plus chemotherapy and anti-angiogenic therapy (ICI+CT+A), ICI plus chemoradiotherapy (ICI+CRT), ICI plus chemotherapy and anti-HER2 therapy (ICI+CT+H), and dual-ICI therapy (ICI+ICI). Random-effects comparative meta-analyses were conducted separately by strategy, while single-arm analyses provided descriptive absolute estimates.&lt;/p&gt;Results&lt;p&gt;A total of 74 trials, including 16 RCTs and 58 prospective single-arm trials, were included. In randomized comparisons, ICI+CT was associated with improved pCR (RR, 3.01; 95% CI, 2.19-4.15) and MPR (RR, 1.59; 95% CI, 1.36-1.85) and, in perioperative trials, OS (HR, 0.81; 95% CI, 0.70-0.93) and EFS (HR, 0.74; 95% CI, 0.66-0.83) compared with chemotherapy. ICI+CT+A was associated with improved pCR (RR, 3.43; 95% CI, 1.85-6.37) and MPR (RR, 1.40; 95% CI, 1.12-1.76), but survival evidence was limited to one phase II RCT reporting OS. Comparative evidence for ICI+CRT was limited to one small RCT. Evidence for ICI+CT+H and ICI+ICI was derived mainly from small biomarker-selected noncomparative studies.&lt;/p&gt;Conclusions&lt;p&gt;Evidence differed substantially across the five strategies. ICI+CT was associated with improved pCR and MPR and, in perioperative RCTs, OS and EFS; it had the largest and most mature randomized evidence base. ICI+CT+A was associated with improved pCR and MPR, whereas comparative evidence for ICI+CRT, ICI+CT+H, and ICI+ICI remained limited. Further comparative trials are required, particularly for safety and long-term survival.&lt;/p&gt;Systematic review registration&lt;p&gt;https://www.crd.york.ac.uk/PROSPERO/view/CRD420251271789, identifier CRD420251271789.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-25T05:33:45Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.3389/fimmu.2026.1909466.s001</dc:identifier>
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          <dc:rights>CC BY 4.0</dc:rights>
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