<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Lee JM</submitter><funding>BLRD VA</funding><funding>Thoracic Surgery Foundation for Research and Education NIH NCI</funding><funding>NCATS NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>NCI NIH HHS</funding><funding>VA</funding><funding>NIH NCATS</funding><funding>CSRD VA</funding><funding>NIH NCI</funding><pagination>4556-4568</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5599263</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>23(16)</volume><pubmed_abstract>&lt;b>Purpose:&lt;/b> A phase I study was conducted to determine safety, clinical efficacy, and antitumor immune responses in patients with advanced non-small cell lung carcinoma (NSCLC) following intratumoral administration of autologous dendritic cells (DC) transduced with an adenoviral (Ad) vector expressing the &lt;i>CCL21&lt;/i> gene (Ad-CCL21-DC). We evaluated safety and tumor antigen-specific immune responses following &lt;i>in situ&lt;/i> vaccination (ClinicalTrials.gov: NCT01574222).&lt;b>Experimental Design:&lt;/b> Sixteen stage IIIB/IV NSCLC subjects received two vaccinations (1 × 10&lt;sup>6&lt;/sup>, 5 × 10&lt;sup>6&lt;/sup>, 1 × 10&lt;sup>7&lt;/sup>, or 3 × 10&lt;sup>7&lt;/sup> DCs/injection) by CT- or bronchoscopic-guided intratumoral injections (days 0 and 7). Immune responses were assessed by tumor antigen-specific peri</pubmed_abstract><journal>Clinical cancer research : an official journal of the American Association for Cancer Research</journal><pubmed_title>Phase I Trial of Intratumoral Injection of &lt;i>CCL21&lt;/i> Gene-Modified Dendritic Cells in Lung Cancer Elicits Tumor-Specific Immune Responses and CD8&lt;sup>+&lt;/sup> T-cell Infiltration.</pubmed_title><pmcid>PMC5599263</pmcid><funding_grant_id>U01 CA196408</funding_grant_id><funding_grant_id>1I01CX000345-01</funding_grant_id><funding_grant_id>NCIK23 CA131577</funding_grant_id><funding_grant_id>U01 CA214182</funding_grant_id><funding_grant_id>UL1 TR001881</funding_grant_id><funding_grant_id>NCIR21 CA105705</funding_grant_id><funding_grant_id>I01 BX000359</funding_grant_id><funding_grant_id>P50 CA090388</funding_grant_id><funding_grant_id>T32 CA009120</funding_grant_id><funding_grant_id>R01 CA085686</funding_grant_id><funding_grant_id>UL1-TR001881</funding_grant_id><funding_grant_id>T32 HL072752</funding_grant_id><funding_grant_id>NCI5 K12 CA076905</funding_grant_id><funding_grant_id>R01 CA208403</funding_grant_id><funding_grant_id>I01 CX000345</funding_grant_id><funding_grant_id>NCIL30 CA142223</funding_grant_id><funding_grant_id>R21 CA105705</funding_grant_id><pubmed_authors>Lee S</pubmed_authors><pubmed_authors>Walser TC</pubmed_authors><pubmed_authors>Wang G</pubmed_authors><pubmed_authors>Lin Y</pubmed_authors><pubmed_authors>Marincola FM</pubmed_authors><pubmed_authors>Schaue D</pubmed_authors><pubmed_authors>Lee G</pubmed_authors><pubmed_authors>Suh R</pubmed_authors><pubmed_authors>Goldman JW</pubmed_authors><pubmed_authors>Dubinett SM</pubmed_authors><pubmed_authors>Lee JM</pubmed_authors><pubmed_authors>Salehi-Rad R</pubmed_authors><pubmed_authors>Park SJ</pubmed_authors><pubmed_authors>Abtin F</pubmed_authors><pubmed_authors>Wallace WD</pubmed_authors><pubmed_authors>Lee MH</pubmed_authors><pubmed_authors>Sharma S</pubmed_authors><pubmed_authors>Garon E</pubmed_authors><pubmed_authors>Rosen F</pubmed_authors><pubmed_authors>Yanagawa J</pubmed_authors><pubmed_authors>Elashoff DA</pubmed_authors><pubmed_authors>Adams S</pubmed_authors><pubmed_authors>Reckamp KL</pubmed_authors><pubmed_authors>Baratelli FE</pubmed_authors><pubmed_authors>Zeng G</pubmed_authors><pubmed_authors>Tumeh PC</pubmed_authors></additional><is_claimable>false</is_claimable><name>Phase I Trial of Intratumoral Injection of &lt;i>CCL21&lt;/i> Gene-Modified Dendritic Cells in Lung Cancer Elicits Tumor-Specific Immune Responses and CD8&lt;sup>+&lt;/sup> T-cell Infiltration.</name><description>&lt;b>Purpose:&lt;/b> A phase I study was conducted to determine safety, clinical efficacy, and antitumor immune responses in patients with advanced non-small cell lung carcinoma (NSCLC) following intratumoral administration of autologous dendritic cells (DC) transduced with an adenoviral (Ad) vector expressing the &lt;i>CCL21&lt;/i> gene (Ad-CCL21-DC). We evaluated safety and tumor antigen-specific immune responses following &lt;i>in situ&lt;/i> vaccination (ClinicalTrials.gov: NCT01574222).&lt;b>Experimental Design:&lt;/b> Sixteen stage IIIB/IV NSCLC subjects received two vaccinations (1 × 10&lt;sup>6&lt;/sup>, 5 × 10&lt;sup>6&lt;/sup>, 1 × 10&lt;sup>7&lt;/sup>, or 3 × 10&lt;sup>7&lt;/sup> DCs/injection) by CT- or bronchoscopic-guided intratumoral injections (days 0 and 7). Immune responses were assessed by tumor antigen-specific peri</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Aug</publication><modification>2026-05-04T17:14:50.243Z</modification><creation>2019-03-26T23:51:08Z</creation></dates><accession>S-EPMC5599263</accession><cross_references><pubmed>28468947</pubmed><doi>10.1158/1078-0432.CCR-16-2821</doi><doi>10.1158/1078-0432.ccr-16-2821</doi></cross_references></HashMap>