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        <identifier>oai:figshare.com:article/34037680</identifier>
        <datestamp>2026-10-01T01:48:22Z</datestamp>
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          <dc:title>Hepatic arterial infusion chemotherapy plus lenvatinib with or without PD-1 inhibition for unresectable hepatocellular carcinoma: a retrospective cohort study</dc:title>
          <dc:creator>Haidong Yu (101810)</dc:creator>
          <dc:creator>Cunkai Ma (25147522)</dc:creator>
          <dc:creator>Cairang Yangdan (25147525)</dc:creator>
          <dc:creator>Haiming Yang (11192941)</dc:creator>
          <dc:creator>Xiaolei Xu (81386)</dc:creator>
          <dc:subject>Medicine</dc:subject>
          <dc:subject>Biotechnology</dc:subject>
          <dc:subject>Immunology</dc:subject>
          <dc:subject>Cancer</dc:subject>
          <dc:subject>Science Policy</dc:subject>
          <dc:subject>Hepatic arterial infusion chemotherapy</dc:subject>
          <dc:subject>lenvatinib</dc:subject>
          <dc:subject>PD-1 inhibition</dc:subject>
          <dc:subject>unresectable hepatocellular carcinoma</dc:subject>
          <dc:subject>propensity score matching</dc:subject>
          <dc:subject>retrospective study</dc:subject>
          <dc:description>&lt;p&gt;The benefit of adding programmed cell death protein 1 (PD-1) blockade to hepatic arterial infusion chemotherapy (HAIC) plus lenvatinib for unresectable hepatocellular carcinoma remains uncertain. This single-center retrospective cohort study included 373 patients. After propensity score matching, 107 patients treated with HAIC plus lenvatinib alone and 107 patients treated with a PD-1 inhibitor were analyzed. Outcomes included overall survival (OS), progression-free survival (PFS), tumor response, and adverse events. PD-1 therapy was associated with longer OS (median, 22.5 vs 13.8 months; adjusted hazard ratio, 0.61; 95% CI, 0.40–0.94; &lt;i&gt;p&lt;/i&gt; = 0.025) and a higher objective response rate (52.3% vs 40.2%, &lt;i&gt;p&lt;/i&gt; = 0.075). The adjusted PFS difference was significant (hazard ratio, 0.67; 95% CI, 0.48–0.92; &lt;i&gt;p&lt;/i&gt; = 0.015). No statistically significant differences in survival were detected among sintilimab, camrelizumab, and pembrolizumab. Grade 3–4 adverse events were comparable. Adding PD-1 blockade was associated with longer OS without substantially increasing severe toxicity.&lt;/p&gt;</dc:description>
          <dc:date>2026-10-01T01:48:22Z</dc:date>
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          <dc:identifier>10.6084/m9.figshare.34037680.v1</dc:identifier>
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          <dc:rights>CC BY 4.0</dc:rights>
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