<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Fang J</submitter><funding>Major National Science and Technology Projects, China</funding><funding>Shanghai Cell Therapy Group Corporation</funding><pagination>e001162</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7887368</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(2)</volume><pubmed_abstract>Epithelial ovarian cancer (EOC) is the leading cause of death among gynecological malignancies in China. In particular, advanced/refractory ovarian cancer lacks effective targeted therapies due to the immunosuppressive and proangiogenic tumor microenvironment. Mesothelin (MSLN) has been found to be highly expressive in most EOC. Targeting MSLN by antibodies or chimeric antigen receptor-modified T (CAR-T) cells and immune checkpoint blockades as well as apatinib, an anti-angiogenic drug, have been used in patients with refractory ovarian cancer. Apatinib was reported to promote the infiltration of CD8&lt;sup>+&lt;/sup> T cells in lung cancer. However, the combination therapy of CAR-T secreting anti-PD-1 antibody with apatinib in EOC has not been reported.&lt;h4>Case presentation&lt;/h4>Here we report a</pubmed_abstract><journal>Journal for immunotherapy of cancer</journal><pubmed_title>αPD-1-mesoCAR-T cells partially inhibit the growth of advanced/refractory ovarian cancer in a patient along with daily apatinib.</pubmed_title><pmcid>PMC7887368</pmcid><funding_grant_id>2018ZX10302207-003; 2019YFC1316202</funding_grant_id><funding_grant_id>BZ1903</funding_grant_id><pubmed_authors>Fang J</pubmed_authors><pubmed_authors>Guo X</pubmed_authors><pubmed_authors>Chu W</pubmed_authors><pubmed_authors>Xu Q</pubmed_authors><pubmed_authors>Ding N</pubmed_authors><pubmed_authors>Wang H</pubmed_authors><pubmed_authors>Lin Z</pubmed_authors><pubmed_authors>Yuan M</pubmed_authors><pubmed_authors>Sun Y</pubmed_authors><pubmed_authors>Li Z</pubmed_authors><pubmed_authors>Zhang Z</pubmed_authors><pubmed_authors>Mao W</pubmed_authors><pubmed_authors>Qin H</pubmed_authors><pubmed_authors>Qin F</pubmed_authors><pubmed_authors>Qian Q</pubmed_authors><pubmed_authors>Xie B</pubmed_authors></additional><is_claimable>false</is_claimable><name>αPD-1-mesoCAR-T cells partially inhibit the growth of advanced/refractory ovarian cancer in a patient along with daily apatinib.</name><description>Epithelial ovarian cancer (EOC) is the leading cause of death among gynecological malignancies in China. In particular, advanced/refractory ovarian cancer lacks effective targeted therapies due to the immunosuppressive and proangiogenic tumor microenvironment. Mesothelin (MSLN) has been found to be highly expressive in most EOC. Targeting MSLN by antibodies or chimeric antigen receptor-modified T (CAR-T) cells and immune checkpoint blockades as well as apatinib, an anti-angiogenic drug, have been used in patients with refractory ovarian cancer. Apatinib was reported to promote the infiltration of CD8&lt;sup>+&lt;/sup> T cells in lung cancer. However, the combination therapy of CAR-T secreting anti-PD-1 antibody with apatinib in EOC has not been reported.&lt;h4>Case presentation&lt;/h4>Here we report a</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Feb</publication><modification>2026-06-14T07:47:35.243Z</modification><creation>2024-11-15T19:16:44.528Z</creation></dates><accession>S-EPMC7887368</accession><cross_references><pubmed>33589520</pubmed><doi>10.1136/jitc-2020-001162</doi></cross_references></HashMap>