<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Metildi CA</submitter><funding>NCI NIH HHS</funding><pagination>1405-11</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4334378</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>21(4)</volume><pubmed_abstract>We have developed a method of distinguishing normal tissue from pancreatic cancer in vivo using fluorophore-conjugated antibody to carcinoembryonic antigen (CEA). The objective of this study was to evaluate whether fluorescence-guided surgery (FGS) with a fluorophore-conjugated antibody to CEA, to highlight the tumor, can improve surgical resection and increase disease-free survival (DFS) and overall survival (OS) in orthotopic mouse models of human pancreatic cancer.We established nude-mouse models of human pancreatic cancer with surgical orthotopic implantation of the human BxPC-3 pancreatic cancer. Orthotopic tumors were allowed to develop for 2 weeks. Mice then underwent bright-light surgery (BLS) or FGS 24 h after intravenous injection of anti-CEA-Alexa Fluor 488. Completeness of resection was assessed from postoperative imaging. Mice were followed postoperatively until premorbid to determine DFS and OS.Complete resection was achieved in 92 % of mice in the FGS group compared to 45.5 % in the BLS group (p = 0.001). FGS resulted in a smaller postoperative tumor burden (p = 0.01). Cure rates with FGS compared to BLS improved from 4.5 to 40 %, respectively (p = 0.01), and 1-year postoperative survival rates increased from 0 % with BLS to 28 % with FGS (p = 0.01). Median DFS increased from 5 weeks with BLS to 11 weeks with FGS (p = 0.0003). Median OS increased from 13.5 weeks with BLS to 22 weeks with FGS (p = 0.001).FGS resulted in greater cure rates and longer DFS and OS using a fluorophore-conjugated anti-CEA antibody. FGS has potential to improve the surgical treatment of pancreatic cancer.</pubmed_abstract><journal>Annals of surgical oncology</journal><pubmed_title>Fluorescence-guided surgery with a fluorophore-conjugated antibody to carcinoembryonic antigen (CEA), that highlights the tumor, improves surgical resection and increases survival in orthotopic mouse models of human pancreatic cancer.</pubmed_title><pmcid>PMC4334378</pmcid><funding_grant_id>T32 CA121938</funding_grant_id><funding_grant_id>R01 CA132971</funding_grant_id><funding_grant_id>CA121938-5</funding_grant_id><funding_grant_id>CA132971</funding_grant_id><funding_grant_id>P30 CA023100</funding_grant_id><funding_grant_id>CA142669</funding_grant_id><funding_grant_id>R01 CA142669</funding_grant_id><pubmed_authors>Metildi CA</pubmed_authors><pubmed_authors>Pu M</pubmed_authors><pubmed_authors>Moossa AR</pubmed_authors><pubmed_authors>Luiken GA</pubmed_authors><pubmed_authors>Messer KA</pubmed_authors><pubmed_authors>Hoffman RM</pubmed_authors><pubmed_authors>Bouvet M</pubmed_authors><pubmed_authors>Kaushal S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Fluorescence-guided surgery with a fluorophore-conjugated antibody to carcinoembryonic antigen (CEA), that highlights the tumor, improves surgical resection and increases survival in orthotopic mouse models of human pancreatic cancer.</name><description>We have developed a method of distinguishing normal tissue from pancreatic cancer in vivo using fluorophore-conjugated antibody to carcinoembryonic antigen (CEA). The objective of this study was to evaluate whether fluorescence-guided surgery (FGS) with a fluorophore-conjugated antibody to CEA, to highlight the tumor, can improve surgical resection and increase disease-free survival (DFS) and overall survival (OS) in orthotopic mouse models of human pancreatic cancer.We established nude-mouse models of human pancreatic cancer with surgical orthotopic implantation of the human BxPC-3 pancreatic cancer. Orthotopic tumors were allowed to develop for 2 weeks. Mice then underwent bright-light surgery (BLS) or FGS 24 h after intravenous injection of anti-CEA-Alexa Fluor 488. Completeness of resection was assessed from postoperative imaging. Mice were followed postoperatively until premorbid to determine DFS and OS.Complete resection was achieved in 92 % of mice in the FGS group compared to 45.5 % in the BLS group (p = 0.001). FGS resulted in a smaller postoperative tumor burden (p = 0.01). Cure rates with FGS compared to BLS improved from 4.5 to 40 %, respectively (p = 0.01), and 1-year postoperative survival rates increased from 0 % with BLS to 28 % with FGS (p = 0.01). Median DFS increased from 5 weeks with BLS to 11 weeks with FGS (p = 0.0003). Median OS increased from 13.5 weeks with BLS to 22 weeks with FGS (p = 0.001).FGS resulted in greater cure rates and longer DFS and OS using a fluorophore-conjugated anti-CEA antibody. FGS has potential to improve the surgical treatment of pancreatic cancer.</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014 Apr</publication><modification>2020-10-29T11:07:41Z</modification><creation>2019-03-27T01:46:45Z</creation></dates><accession>S-EPMC4334378</accession><cross_references><pubmed>24499827</pubmed><doi>10.1245/s10434-014-3495-y</doi></cross_references></HashMap>