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        <datestamp>2026-09-18T05:28:41Z</datestamp>
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          <dc:title>Supplementary file 2_Efficacy and safety of thymosin α1 combined with chemotherapy for gastric cancer: a systematic review and meta-analysis of randomized controlled trials.docx</dc:title>
          <dc:creator>Zekun Wang (9394226)</dc:creator>
          <dc:creator>Tao Sun (91038)</dc:creator>
          <dc:creator>Haoran Qu (6804689)</dc:creator>
          <dc:creator>Ruping Zhao (22596803)</dc:creator>
          <dc:creator>Xishen Shan (22596806)</dc:creator>
          <dc:creator>Yu Liu (6938)</dc:creator>
          <dc:creator>Yuling Zheng (123026)</dc:creator>
          <dc:subject>Genetic Immunology</dc:subject>
          <dc:subject>chemotherapy</dc:subject>
          <dc:subject>gastric cancer</dc:subject>
          <dc:subject>grade</dc:subject>
          <dc:subject>immunomodulation</dc:subject>
          <dc:subject>thymosin α1</dc:subject>
          <dc:subject>TSA</dc:subject>
          <dc:description>Objective&lt;p&gt;To systematically evaluate the efficacy and safety of thymosin α1 combined with chemotherapy in the treatment of gastric cancer.&lt;/p&gt;Methods&lt;p&gt;A systematic search of 8 electronic databases was conducted to identify relevant RCTs. Meta-analysis was performed using Stata 18.0. Meta-regression, subgroup analyses, sensitivity analyses, and publication bias analyses were conducted to further examine results, and reliability of findings was assessed using TSA and GRADE.&lt;/p&gt;Results&lt;p&gt;20 RCTs involving 1,704 patients were included. Meta-analysis results showed that, thymosin α1 combined with chemotherapy was associated with higher ORR (RR = 1.39), DCR (RR = 1.16), and KPS scores (WMD = 8.27). Regarding immune function, combination therapy resulted in higher CD3&lt;sup&gt;+&lt;/sup&gt;% (WMD = 7.73), CD4&lt;sup&gt;+&lt;/sup&gt;% (WMD = 6.87), CD4&lt;sup&gt;+&lt;/sup&gt;/CD8&lt;sup&gt;+&lt;/sup&gt; (WMD = 0.42), and NK cell (WMD = 4.73). Regarding tumor markers, combination therapy resulted in lower levels of CEA (WMD = −5.48) and CA199 (WMD = −9.06). Regarding inflammatory factors, combination therapy may reduce levels of MMP-2, MMP-9, IL-4, and IL-10, while increasing levels of IFN-γ and TNF-α. Regarding safety, combination therapy was associated with reductions in gastrointestinal reactions (RR = 0.63), myelosuppression (RR = 0.60), abnormal liver function (RR = 0.54), and neurotoxicity (RR = 0.47). However, included RCTs did not systematically report long-term survival outcomes, and their methodological quality was limited; and GRADE indicated that quality of evidence for outcomes ranged from very low to moderate.&lt;/p&gt;Conclusion&lt;p&gt;The combination of thymosin α1 with chemotherapy is associated with improved short-term efficacy, enhanced immune function, improved quality of life, and a reduced incidence of adverse reactions in patients with gastric cancer, indicating good potential for clinical application. However, it remains unclear whether this approach can provide long-term benefits for patients with gastric cancer. Furthermore, given that studies included were all small-sample studies conducted in China and were of limited quality, certainty of evidence is low; these conclusions require further validation through additional high-quality studies.&lt;/p&gt;Systematic Review Registration&lt;p&gt;https://www.crd.york.ac.uk/PROSPERO/, Identifier CRD420261282679.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-18T05:28:41Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.3389/fimmu.2026.1884797.s002</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Supplementary_file_2_Efficacy_and_safety_of_thymosin_1_combined_with_chemotherapy_for_gastric_cancer_a_systematic_review_and_meta-analysis_of_randomized_controlled_trials_docx/33920344</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
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