<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>17</volume><submitter>Zhang F</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>The effect of claudin 18.2 (CLDN18.2) expression on the outcomes of a first-line immune checkpoint inhibitor (ICI)-containing chemotherapy (ICI-chemo) in patients with human epidermal growth factor receptor 2 (HER2)-negative, proficient mismatch repair (pMMR), and programmed death-ligand 1 (PD-L1)-expressing metastatic or recurrent gastric or gastroesophageal junction cancers (mGC/GEJC) remains unclear.&lt;h4>Objectives&lt;/h4>We assessed the effects of CLDN18.2 expression on the outcomes of first-line ICI-containing chemotherapy in patients with HER2-negative, pMMR, and PD-L1-expressing mGC/GEJC.&lt;h4>Patients and methods&lt;/h4>Medical records of patients with HER2-negative, pMMR, and PD-L1 combined positive score (CPS) ⩾1 unresectable/metastatic or recurrent GC/GEJC who received first-line ICI-chemo or chemotherapy alone (chemo-alone) between January 2016 and August 2024 were retrospectively analyzed. The impact of CLDN18.2 status on the clinical outcomes was evaluated in patients receiving ICI-chemo and chemo-alone to assess the prognostic significance of CLDN18.2 in the absence of ICI.&lt;h4>Results&lt;/h4>A total of 150 patients were treated with ICI-chemo, whereas 313 patients received chemo-alone. CLDN18.2 positivity (⩾2+ in ⩾75% tumor cells) was identified in 42 patients (28.0%) in the ICI-chemo group and 94 patients (30.0%) in the chemo-alone group. There were no significant differences in the objective response rate (ORR; 68.3% vs 70.3%, &lt;i>p&lt;/i> = 0.842), disease control rate (DCR; 92.7% vs 94.1%, &lt;i>p&lt;/i> = 0.718), progression-free survival (PFS; hazard ratio (HR) 1.01, &lt;i>p&lt;/i> = 0.955), or overall survival (OS; HR 1.12, &lt;i>p&lt;/i> = 0.615) between CLDN18.2-positive and CLDN18.2-negative patients in the ICI-chemo group. Similarly, the DCR, ORR, PFS, and OS outcomes were comparable between the CLDN18.2-positive and -negative patients in the chemo-alone group.&lt;h4>Conclusion&lt;/h4>CLDN18.2 expression exerted no impact on outcomes of first-line ICI-chemo and chemo-alone in patients with HER2-negative, pMMR, and PD-L1 CPS ⩾1 mGC/GEJC.</pubmed_abstract><journal>Therapeutic advances in medical oncology</journal><pagination>17588359251369042</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12450271</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Impact of claudin 18.2 expression on treatment outcomes of first-line immunochemotherapy in patients with HER2-negative, proficient MMR, PD-L1 CPS ⩾1 metastatic gastric/gastroesophageal junction cancer.</pubmed_title><pmcid>PMC12450271</pmcid><pubmed_authors>Miyashita Y</pubmed_authors><pubmed_authors>Zhang F</pubmed_authors><pubmed_authors>Yamamoto K</pubmed_authors><pubmed_authors>Nakayama I</pubmed_authors><pubmed_authors>Ushiyama S</pubmed_authors><pubmed_authors>Kojima T</pubmed_authors><pubmed_authors>Kawazoe A</pubmed_authors><pubmed_authors>Sakamoto N</pubmed_authors><pubmed_authors>Shitara K</pubmed_authors><pubmed_authors>Okemoto D</pubmed_authors><pubmed_authors>Matsubara Y</pubmed_authors><pubmed_authors>Okazaki U</pubmed_authors><pubmed_authors>Mishima S</pubmed_authors><pubmed_authors>Kobayashi A</pubmed_authors><pubmed_authors>Sato S</pubmed_authors><pubmed_authors>Hashimoto T</pubmed_authors><pubmed_authors>Jubashi A</pubmed_authors><pubmed_authors>Kuboki Y</pubmed_authors><pubmed_authors>Nakamura Y</pubmed_authors><pubmed_authors>Kotani D</pubmed_authors><pubmed_authors>Kuwata T</pubmed_authors><pubmed_authors>Bando H</pubmed_authors><pubmed_authors>Yoshino T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Impact of claudin 18.2 expression on treatment outcomes of first-line immunochemotherapy in patients with HER2-negative, proficient MMR, PD-L1 CPS ⩾1 metastatic gastric/gastroesophageal junction cancer.</name><description>&lt;h4>Background&lt;/h4>The effect of claudin 18.2 (CLDN18.2) expression on the outcomes of a first-line immune checkpoint inhibitor (ICI)-containing chemotherapy (ICI-chemo) in patients with human epidermal growth factor receptor 2 (HER2)-negative, proficient mismatch repair (pMMR), and programmed death-ligand 1 (PD-L1)-expressing metastatic or recurrent gastric or gastroesophageal junction cancers (mGC/GEJC) remains unclear.&lt;h4>Objectives&lt;/h4>We assessed the effects of CLDN18.2 expression on the outcomes of first-line ICI-containing chemotherapy in patients with HER2-negative, pMMR, and PD-L1-expressing mGC/GEJC.&lt;h4>Patients and methods&lt;/h4>Medical records of patients with HER2-negative, pMMR, and PD-L1 combined positive score (CPS) ⩾1 unresectable/metastatic or recurrent GC/GEJC who received first-line ICI-chemo or chemotherapy alone (chemo-alone) between January 2016 and August 2024 were retrospectively analyzed. The impact of CLDN18.2 status on the clinical outcomes was evaluated in patients receiving ICI-chemo and chemo-alone to assess the prognostic significance of CLDN18.2 in the absence of ICI.&lt;h4>Results&lt;/h4>A total of 150 patients were treated with ICI-chemo, whereas 313 patients received chemo-alone. CLDN18.2 positivity (⩾2+ in ⩾75% tumor cells) was identified in 42 patients (28.0%) in the ICI-chemo group and 94 patients (30.0%) in the chemo-alone group. There were no significant differences in the objective response rate (ORR; 68.3% vs 70.3%, &lt;i>p&lt;/i> = 0.842), disease control rate (DCR; 92.7% vs 94.1%, &lt;i>p&lt;/i> = 0.718), progression-free survival (PFS; hazard ratio (HR) 1.01, &lt;i>p&lt;/i> = 0.955), or overall survival (OS; HR 1.12, &lt;i>p&lt;/i> = 0.615) between CLDN18.2-positive and CLDN18.2-negative patients in the ICI-chemo group. Similarly, the DCR, ORR, PFS, and OS outcomes were comparable between the CLDN18.2-positive and -negative patients in the chemo-alone group.&lt;h4>Conclusion&lt;/h4>CLDN18.2 expression exerted no impact on outcomes of first-line ICI-chemo and chemo-alone in patients with HER2-negative, pMMR, and PD-L1 CPS ⩾1 mGC/GEJC.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025</publication><modification>2026-06-03T17:17:30.72Z</modification><creation>2026-04-29T03:12:45.063Z</creation></dates><accession>S-EPMC12450271</accession><cross_references><pubmed>40985041</pubmed><doi>10.1177/17588359251369042</doi></cross_references></HashMap>