<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wang Y</submitter><funding>Natural Science Foundation of Beijing Municipality (Beijing Natural Science Foundation)</funding><funding>Natural Science Foundation of Beijing Municipality</funding><funding>National Natural Science Foundation of China</funding><funding>National Natural Science Foundation of China (National Science Foundation of China)</funding><pagination>100</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11906745</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>10(1)</volume><pubmed_abstract>Alpha-fetoprotein-producing gastric or gastro-esophageal junction (AFP-G/GEJ) cancer, a rare gastric cancer subtype, exhibits increased angiogenesis and more immunosuppression than non-AFP-G/GEJ cancer. The potential benefits of anti-angiogenic agents and immunotherapy for this specific subtype remain unknown. This multi-center, single-arm, phase 2 trial (ClinicalTrials.gov NCT04609176) evaluated the antitumor activity, safety, and biomarkers of camrelizumab plus apatinib and S-1 and oxaliplatin (SOX), followed by maintenance treatment with camrelizumab plus apatinib, as a first-line treatment in patients with AFP-G/GEJ adenocarcinoma. Primary endpoint was the confirmed objective response rate (ORR) per RECIST v1.1 in the full analysis set. Secondary endpoints were disease control rate (DC</pubmed_abstract><journal>Signal transduction and targeted therapy</journal><pubmed_title>PD-1 antibody camrelizumab plus apatinib and SOX as first-line treatment in patients with AFP-producing gastric or gastro-esophageal junction adenocarcinoma (CAP 06): a multi-center, single-arm, phase 2 trial.</pubmed_title><pmcid>PMC11906745</pmcid><funding_grant_id>Z20J00105</funding_grant_id><funding_grant_id>82272627</funding_grant_id><funding_grant_id>L234003</funding_grant_id><pubmed_authors>Shen L</pubmed_authors><pubmed_authors>Hou Z</pubmed_authors><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Gu Y</pubmed_authors><pubmed_authors>Wang C</pubmed_authors><pubmed_authors>Lu Z</pubmed_authors><pubmed_authors>Kou H</pubmed_authors><pubmed_authors>Peng Z</pubmed_authors><pubmed_authors>Yuan J</pubmed_authors><pubmed_authors>Chong X</pubmed_authors><pubmed_authors>Lu M</pubmed_authors><pubmed_authors>Lu J</pubmed_authors><pubmed_authors>Cao Y</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Chen Y</pubmed_authors><pubmed_authors>Chen X</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Gong J</pubmed_authors><pubmed_authors>Zhang C</pubmed_authors><pubmed_authors>Qi C</pubmed_authors><pubmed_authors>Zhou J</pubmed_authors></additional><is_claimable>false</is_claimable><name>PD-1 antibody camrelizumab plus apatinib and SOX as first-line treatment in patients with AFP-producing gastric or gastro-esophageal junction adenocarcinoma (CAP 06): a multi-center, single-arm, phase 2 trial.</name><description>Alpha-fetoprotein-producing gastric or gastro-esophageal junction (AFP-G/GEJ) cancer, a rare gastric cancer subtype, exhibits increased angiogenesis and more immunosuppression than non-AFP-G/GEJ cancer. The potential benefits of anti-angiogenic agents and immunotherapy for this specific subtype remain unknown. This multi-center, single-arm, phase 2 trial (ClinicalTrials.gov NCT04609176) evaluated the antitumor activity, safety, and biomarkers of camrelizumab plus apatinib and S-1 and oxaliplatin (SOX), followed by maintenance treatment with camrelizumab plus apatinib, as a first-line treatment in patients with AFP-G/GEJ adenocarcinoma. Primary endpoint was the confirmed objective response rate (ORR) per RECIST v1.1 in the full analysis set. Secondary endpoints were disease control rate (DC</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Mar</publication><modification>2026-04-08T19:53:21.772Z</modification><creation>2025-04-05T22:08:21.422Z</creation></dates><accession>S-EPMC11906745</accession><cross_references><pubmed>40082418</pubmed><doi>10.1038/s41392-025-02193-z</doi></cross_references></HashMap>