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<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="research-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Current Gene Therapy</journal-id><journal-title-group><journal-title xml:lang="en">Current Gene Therapy</journal-title><trans-title-group xml:lang="ru"><trans-title>Current Gene Therapy</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1566-5232</issn><issn publication-format="electronic">1875-5631</issn><publisher><publisher-name xml:lang="en">Bentham Science</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">643970</article-id><article-id pub-id-type="doi">10.2174/0115665232247694230921060213</article-id><article-categories><subj-group subj-group-type="toc-heading"><subject>Life Sciences</subject></subj-group><subj-group subj-group-type="article-type"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">A Retrospective Analysis of the Lauren Classification in the Choice of XELOX or SOX as an Adjuvant Chemotherapy for Gastric Cancer</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Wang</surname><given-names>Ke</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>Yu</surname><given-names>Yuanyuan</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name><surname>Zhao</surname><given-names>Jian</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff3"/></contrib><contrib contrib-type="author"><name><surname>Meng</surname><given-names>Qianhao</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff4"/></contrib><contrib contrib-type="author"><name><surname>Xu</surname><given-names>Chang</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff4"/></contrib><contrib contrib-type="author"><name><surname>Ren</surname><given-names>Jing</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff4"/></contrib><contrib contrib-type="author"><name><surname>Zhang</surname><given-names>Yanqiao</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff5"/></contrib><contrib contrib-type="author"><name><surname>Wang</surname><given-names>Yusheng</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff6"/></contrib><contrib contrib-type="author"><name><surname>Wang</surname><given-names>Guangyu</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff4"/></contrib></contrib-group><aff id="aff1"><institution>Department of Gastrointestinal Medical Oncology, The Third Affiliated Hospital of Harbin Medical University Cancer Hospital,</institution></aff><aff id="aff2"><institution>Department of Gastrointestinal Medical Oncology, The Third Affiliated Hospital of Harbin Medical University Cancer Hospital</institution></aff><aff id="aff3"><institution>Department of Digestive, Shanxi Province Cancer Hospital/ Shanxi Hospital Affiliated to Cancer Hospital, Chinese Academy of Medical Sciences/Cancer Hospital Affiliated to Shanxi Medical University</institution></aff><aff id="aff4"><institution>Department of Gastrointestinal Medical Oncology,, The Third Affiliated Hospital of Harbin Medical University Cancer Hospital</institution></aff><aff id="aff5"><institution>Department of Gastrointestinal Medical Oncology,, The Third Affiliated Hospital of Harbin Medical University Cancer Hospital,</institution></aff><aff id="aff6"><institution>Department of Digestive, Shanxi Province Cancer Hospital/ Shanxi Hospital Affiliated to Cancer Hospital, Chinese Academy of Medical Sciences/Cancer Hospital Affiliated to Shanxi Medical University,</institution></aff><pub-date date-type="pub" iso-8601-date="2024-02-01" publication-format="electronic"><day>01</day><month>02</month><year>2024</year></pub-date><volume>24</volume><issue>2</issue><issue-title xml:lang="ru"/><fpage>147</fpage><lpage>158</lpage><history><date date-type="received" iso-8601-date="2025-01-07"><day>07</day><month>01</month><year>2025</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2024, Bentham Science Publishers</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="en">Bentham Science Publishers</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/></permissions><self-uri xlink:href="https://transsyst.ru/1566-5232/article/view/643970">https://transsyst.ru/1566-5232/article/view/643970</self-uri><abstract xml:lang="en"><p id="idm46041443756192">Background:We aim to retrospectively explore the guiding value of the Lauren classification for patients who have undergone D2 gastrectomy to choose oxaliplatin plus capecitabine (XELOX) or oxaliplatin plus S-1 (SOX) as a further systemic treatment after the operation.</p><p id="idm46041443760192">Methods:We collected data of 406 patients with stage III gastric cancer(GC)after radical D2 resection and regularly received XELOX or SOX adjuvant treatment after surgery and followed them for at least five years. According to the Lauren classification, we separated patients out into intestinal type (IT) GC together with non-intestinal type(NIT) GC. According to the chemotherapy regimen, we separated patients into the SOX group together with the XELOX group.</p><p id="idm46041443764160">Results:Among non-intestinal type patients, the 3-year DFS rates in the SOX group and the XELOX group were 72.5%, respectively; 54.5% (P=0.037); The 5-year OS rates were 66.8% and 51.8% respectively (P=0.038), both of which were statistically significant.</p><p id="idm46041443769216">Conclusion:The patients of non-intestinal type GC may benefit from the SOX regimen. Differences were counted without being statistically significant with intestinal-type GC in the SOX or XELOX groups.</p></abstract><kwd-group xml:lang="en"><kwd>Lauren subtype</kwd><kwd>adjuvant chemotherapy</kwd><kwd>gastric cancer</kwd><kwd>capecitabine plus oxaliplatin</kwd><kwd>S- 1 plus oxaliplatin</kwd><kwd>survival.</kwd></kwd-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Sung H, Ferlay J, Siegel RL, et al. Global Cancer Statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 Countries. CA Cancer J Clin 2021; 71(3): 209-49. doi: 10.3322/caac.21660 PMID: 33538338</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Allemani C, Matsuda T, Di Carlo V, et al. Global surveillance of trends in cancer survival 200014 (CONCORD-3): Analysis of individual records for 37 513 025 patients diagnosed with one of 18 cancers from 322 population-based registries in 71 countries. 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