{"doi":"10.1136/jitc-2022-sitc2022.0885","title":"885 Enhancing immune checkpoint inhibitor efficacy with anti-angiogenics in ovarian cancer","abstract":"<h3>Background</h3> Clinical data from our group supports that ovarian cancer (OC) patients respond better to immune checkpoint blockade (ICB) when targeting both PD-1 and CTLA4 compared to anti-PD-1 alone (33% v. 10%, respectively),<sup>1</sup> yet there is still room to improve dual-ICB response. Bevacizumab is approved as a front-line therapy for OC and targets vascular endothelial growth factor A (VEGF-A). VEGF has been shown to have both anti-tumor and immunomodulatory effects as it induces macrophage infiltration and M2 polarization<sup>2</sup> and directly suppresses T-cell activation, proliferation, and cytotoxic activity.<sup>3,4</sup> Here we aim to determine if priming the immunosuppressive tumor microenvironment (TME) with anti-VEGF enhances the response of T-cell stimulating ICB. <h3>Methods</h3> We developed a patient avatar model by administering <i>ex vivo</i> expanded tumor infiltrating lymphocytes (TILs) into immunodeficient mice harboring a patient-matched, patient-derived xenograft (PDX).<sup>5,6</sup> Autologous TIL reactivity was validated by flow cytometry and ELISA. Preclinical <i>in vivo</i> studies were performed to evaluate if the efficacy of dual-ICBs (nivolumab and ipilimumab) could be enhanced through priming with anti-VEGF (bevacizumab). <i>Ex vivo</i> culture systems using donor ascites specimens and viable tumor slices were evaluated to further evaluate this combination in OC. <h3>Results</h3> Six distinct PDX/TIL models were developed. Co-culture of TILs with autologous tumor cells resulted in HLA-dependent IFNγ production by TILs with a parallel impact on TIL activation phenotype. In response to IFNγ, PD-L1 expression was increased on tumor cells, suggesting antitumor activity might be improved via PD-1 blockade.<sup>5</sup> As proof-of-concept, anti-PD-1 efficacy was tested in PDX/TIL models (n=3).<sup>5</sup> Anti-PD-1 reduced tumor burden and increased survival in two models compared to TIL treatment alone. Next, we tested the hypothesis that the efficacy of dual-ICBs could be enhanced through TME priming with anti-VEGF (n=3). Results revealed increased efficacy of dual-ICB with anti-VEGF priming in 2 models. Immunohistochemistry and flow cytometry analysis support that the TILs in the combination ICB +/- anti-VEGF have increased anti-tumor activity. To better delineate the activity of dual-ICB and anti-VEGF in an intact TME, <i>ex vivo</i> cultures were used. OC ascites significantly increased the secretion of T-cell effector and myeloid cell associated immunosuppressive molecules in response to ICB treatment, and CD11b+ tumor associated macrophages (TAMs) significantly reduced T-cell activation. In tumor slice cultures, combination treatment with dual-ICB and anti-VEGF reduced overall tumor burden. <h3>Conclusions</h3> This data supports the notion that, in addition to the effect of anti-VEGF priming, modulation of the immunosuppressive myeloid population may further enhance ICB efficacy. <h3>Acknowledgements</h3> We would like to thank the National Center for Advancing Translational Sciences of the National Institutes of Health (award number TL1TR001880), the Rivkin Center for Ovarian Cancer, the Ovarian Cancer Research Alliance, and the Penn Ovarian Cancer Translational Center of Excellence for funding this research. We would like to acknowledge the UPenn Stem Cell and Xenograft, Histology, and Human Immunology cores. We also thank Benjamin Ferman for his technical support for in in vivo studies. Finally, we would like to acknowledge the patients who volunteered to donate their tissue to the Ovarian Cancer Biotrust Collection. <h3>References</h3> Zamarin, D, <i>et al</i>. Randomized phase II trial of nivolumab versus nivolumab and ipilimumab for recurrent or persistent ovarian cancer: an NRG oncology study. <i>J Clin Oncol</i> 2020;<b>38</b>, 1814–1823, doi:10.1200/JCO.19.02059. Roland CL, <i>et al</i>. Inhibition of vascular endothelial growth factor reduces angiogenesis and modulates","journal":"Regular and Young Investigator Award Abstracts","year":2022,"id":312919,"datarank":0.0,"base_score":0.0,"endowment":0.0,"self_citation_contribution":0.0,"citation_network_contribution":0.0,"self_endowment_contribution":0.0,"citer_contribution":0.0,"corpus_percentile":null,"corpus_rank":null,"citation_count":0,"citer_count":0,"citers_with_citation_signal":0,"citers_with_endowment":0,"datacite_reuse_total":0,"is_dataset":false,"is_dataset_confidence":0.9579,"is_data_producer":false,"deposit_databanks":null,"is_oa":true,"file_count":0,"downloads":0,"has_version_chain":false,"published_date":"2022-01-01","fair_score":null,"fair_percentile":null,"algorithm_id":"datarank_citation_only_1hop_v6","ranking_scope":"data_only","authors":[{"id":1010748,"name":"S. P. Medvedev","orcid":"0000-0002-1520-5549","position":1,"is_corresponding":false},{"id":994512,"name":"Veethika Pandey","orcid":"0000-0002-1476-2124","position":2,"is_corresponding":false},{"id":1433,"name":"Dalia K. Omran","orcid":"0000-0003-4323-2621","position":3,"is_corresponding":false},{"id":1010749,"name":"Matthew Anderson","orcid":"0000-0002-5965-491X","position":4,"is_corresponding":false},{"id":185098,"name":"Lauren E. Schwartz","orcid":null,"position":5,"is_corresponding":false},{"id":231038,"name":"Fiona Simpkins","orcid":"0000-0002-0840-2368","position":6,"is_corresponding":false},{"id":623747,"name":"Daniel J. Powell","orcid":"0000-0002-5966-8908","position":7,"is_corresponding":false},{"id":886243,"name":"Sarah B. Gitto","orcid":"0000-0001-6496-4528","position":0,"is_corresponding":true}],"reference_count":6,"raw_metadata":null,"created_at":"2026-07-19T00:33:40.460845Z","pmid":null,"pmcid":null,"fwci":null,"citation_percentile":null,"influential_citations":0,"oa_status":null,"license":null,"views":0,"total_file_size_bytes":0,"version_count":0,"fair_f":null,"fair_a":null,"fair_i":null,"fair_r":null,"fair_zscore":null,"fair_rationale":null,"fair_model":null,"fair_agent_version":null,"fair_fulltext_source":null,"fair_has_llm":null,"fair_computed_at":null,"clinical_trials":[],"software_tools":[],"db_accessions":[],"linked_datasets":[],"topics":[]}