<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Schwarze JK</submitter><funding>Stichting Tegen Kanker</funding><funding>Oncology Center Vrije Universiteit Brussel</funding><funding>Kom op tegen Kanker (Stand up to Cancer), the Flemish cancer society</funding><pagination>e005141</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9486335</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>10(9)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Intratumoral (IT) myeloid dendritic cells (myDCs) play a pivotal role in initiating antitumor immune responses and relicensing of anti-tumor cytotoxic T lymphocytes within the tumor microenvironment. Talimogene laherparepvec (T-VEC) induces immunogenic cell death, thereby providing maturation signals and enhancing the release of tumor antigens that can be captured and processed by CD1c (BDCA-1)&lt;sup>+&lt;/sup> / CD141 (BDCA-3)&lt;sup>+&lt;/sup> myDCs, in order to reinvigorate the cancer-immunity cycle.&lt;h4>Methods&lt;/h4>In this phase I trial, patients with advanced melanoma who failed standard therapy were eligible for IT injections of ≥1 non-visceral metastases with T-VEC on day 1 followed by IT injection of CD1c (BDCA-1)&lt;sup>+&lt;/sup> myDCs +/- CD141 (BDCA-3)&lt;sup>+&lt;/sup> myDCs on day</pubmed_abstract><journal>Journal for immunotherapy of cancer</journal><pubmed_title>Intratumoral administration of CD1c (BDCA-1)&lt;sup>+&lt;/sup> and CD141 (BDCA-3)&lt;sup>+&lt;/sup> myeloid dendritic cells in combination with talimogene laherparepvec in immune checkpoint blockade refractory advanced melanoma patients: a phase I clinical trial.</pubmed_title><pmcid>PMC9486335</pmcid><funding_grant_id>N/A</funding_grant_id><funding_grant_id>11102</funding_grant_id><funding_grant_id>2016-128</funding_grant_id><pubmed_authors>Awada G</pubmed_authors><pubmed_authors>Cras L</pubmed_authors><pubmed_authors>Neyns B</pubmed_authors><pubmed_authors>Schwarze JK</pubmed_authors><pubmed_authors>Tuyaerts S</pubmed_authors><pubmed_authors>Bagnall C</pubmed_authors><pubmed_authors>Tijtgat J</pubmed_authors><pubmed_authors>Van Riet I</pubmed_authors><pubmed_authors>Vasaturo A</pubmed_authors><pubmed_authors>Forsyth R</pubmed_authors><pubmed_authors>Dufait I</pubmed_authors></additional><is_claimable>false</is_claimable><name>Intratumoral administration of CD1c (BDCA-1)&lt;sup>+&lt;/sup> and CD141 (BDCA-3)&lt;sup>+&lt;/sup> myeloid dendritic cells in combination with talimogene laherparepvec in immune checkpoint blockade refractory advanced melanoma patients: a phase I clinical trial.</name><description>&lt;h4>Background&lt;/h4>Intratumoral (IT) myeloid dendritic cells (myDCs) play a pivotal role in initiating antitumor immune responses and relicensing of anti-tumor cytotoxic T lymphocytes within the tumor microenvironment. Talimogene laherparepvec (T-VEC) induces immunogenic cell death, thereby providing maturation signals and enhancing the release of tumor antigens that can be captured and processed by CD1c (BDCA-1)&lt;sup>+&lt;/sup> / CD141 (BDCA-3)&lt;sup>+&lt;/sup> myDCs, in order to reinvigorate the cancer-immunity cycle.&lt;h4>Methods&lt;/h4>In this phase I trial, patients with advanced melanoma who failed standard therapy were eligible for IT injections of ≥1 non-visceral metastases with T-VEC on day 1 followed by IT injection of CD1c (BDCA-1)&lt;sup>+&lt;/sup> myDCs +/- CD141 (BDCA-3)&lt;sup>+&lt;/sup> myDCs on day</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Sep</publication><modification>2026-06-08T06:46:23.032Z</modification><creation>2026-06-08T03:13:49.734Z</creation></dates><accession>S-EPMC9486335</accession><cross_references><pubmed>36113895</pubmed><doi>10.1136/jitc-2022-005141</doi></cross_references></HashMap>