Electrochemotherapy guided by intraoperative fluorescence imaging for the treatment of inoperable peritoneal micro-metastases
Surgery is often the first therapeutic indication in cancer. Patient survival essentially depends on the completeness of tumor resection. This is a major challenge, particularly in patients with peritoneal carcinomatosis (PC), where tumors are widely disseminated in the large peritoneal cavity. Thes...
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creator | Josserand, V. Kéramidas, M. Lavaud, J. Righini, C. Vollaire, J. Bellard, E. Rols, M.P. Teissié, J. Coll, J.L. Golzio, M. |
description | Surgery is often the first therapeutic indication in cancer. Patient survival essentially depends on the completeness of tumor resection. This is a major challenge, particularly in patients with peritoneal carcinomatosis (PC), where tumors are widely disseminated in the large peritoneal cavity. These small tumors can be difficult to visualize and are often positioned in delicate locations, further increasing the risk of producing serious tissue/organ damage during their ablation. We propose an innovative therapeutic approach based on intraoperative fluorescence (IF) guided electrochemotherapy (ECT) for the treatment of peritoneal micro-metastases. ECT combines the effects of tissue electro-permeabilization (EP) with the administration of an antimitotic agent (bleomycin) that has poor permeability across intact membranes. IF significantly improves the detection of small tumor lesions. ECT is clinically validated for the treatment of cutaneous tumors in animals and humans, but this is the first time that it has been used along with IF imaging for the targeted treatment of peritoneal metastases in a preclinical model.
We set up a murine model of PC that develops secondarily to the resection of a distant primary tumor. Tumor growth and metastasis were finely monitored by non-invasive multimodal imaging (bioluminescence and 3D fluorescence/microCT). Once metastases were detected, mice were randomized into three groups: the ECT group (bleomycin injected intravenously followed by EP) and 2 control groups (bleomycin alone and EP alone). Twenty four hours after the intravenous injection of the tumor targeting agent Angiostamp™700, mice in all groups underwent an abdominal surgery for metastases exploration assisted by fluorescence imaging with the Fluobeam®700 portative device. EP was applied to every nodule detected by IF, except in the bleomycin control group. After surgery, the metastatic invasion was tracked by bioluminescence imaging. In mice treated with bleomycin or EP alone, the metastatic load progressed very rapidly and mice showed no significant difference in lifespan compared to non-operated mice (median lifespan: 27days vs. 25days, respectively). In contrast, the mice treated with ECT displayed a decreased metastatic load and an increased survival rate (median lifespan: 34days). These results provide evidence that IF guided ECT is an effective approach for the treatment of inoperable intraperitoneal micro-metastases.
In this study, we show the effectiv |
doi_str_mv | 10.1016/j.jconrel.2016.05.003 |
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We set up a murine model of PC that develops secondarily to the resection of a distant primary tumor. Tumor growth and metastasis were finely monitored by non-invasive multimodal imaging (bioluminescence and 3D fluorescence/microCT). Once metastases were detected, mice were randomized into three groups: the ECT group (bleomycin injected intravenously followed by EP) and 2 control groups (bleomycin alone and EP alone). Twenty four hours after the intravenous injection of the tumor targeting agent Angiostamp™700, mice in all groups underwent an abdominal surgery for metastases exploration assisted by fluorescence imaging with the Fluobeam®700 portative device. EP was applied to every nodule detected by IF, except in the bleomycin control group. After surgery, the metastatic invasion was tracked by bioluminescence imaging. In mice treated with bleomycin or EP alone, the metastatic load progressed very rapidly and mice showed no significant difference in lifespan compared to non-operated mice (median lifespan: 27days vs. 25days, respectively). In contrast, the mice treated with ECT displayed a decreased metastatic load and an increased survival rate (median lifespan: 34days). These results provide evidence that IF guided ECT is an effective approach for the treatment of inoperable intraperitoneal micro-metastases.
In this study, we show the effectiveness of an innovative approach of electrochemotherapy guided by intraoperative fluorescence imaging for the treatment of inoperable peritoneal micro-metastases in a preclinical model. [Display omitted]</description><identifier>ISSN: 0168-3659</identifier><identifier>EISSN: 1873-4995</identifier><identifier>DOI: 10.1016/j.jconrel.2016.05.003</identifier><identifier>PMID: 27155365</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; Antibiotics, Antineoplastic - administration & dosage ; Antibiotics, Antineoplastic - therapeutic use ; Bleomycin - administration & dosage ; Bleomycin - therapeutic use ; Cancer ; Cell Line, Tumor ; Electrochemotherapy ; Electroporation ; Female ; Fluorescence guided surgery ; Kidney Neoplasms - diagnostic imaging ; Kidney Neoplasms - drug therapy ; Kidney Neoplasms - pathology ; Life Sciences ; Mice, Inbred BALB C ; Optical Imaging ; Peritoneal metastases ; Peritoneal Neoplasms - diagnostic imaging ; Peritoneal Neoplasms - drug therapy ; Peritoneal Neoplasms - secondary ; Tumor targeting ; X-Ray Microtomography</subject><ispartof>Journal of controlled release, 2016-07, Vol.233, p.81-87</ispartof><rights>2016 Elsevier B.V.</rights><rights>Copyright © 2016 Elsevier B.V. All rights reserved.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c479t-7f387be282376175ed0b8e6a748c7ea838c9d4d3d88200cd15290aed72002f073</citedby><cites>FETCH-LOGICAL-c479t-7f387be282376175ed0b8e6a748c7ea838c9d4d3d88200cd15290aed72002f073</cites><orcidid>0000-0002-7470-3708 ; 0009-0000-6055-8119 ; 0000-0003-3100-6272 ; 0000-0002-7588-8062</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0168365916302553$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27155365$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-02390853$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Josserand, V.</creatorcontrib><creatorcontrib>Kéramidas, M.</creatorcontrib><creatorcontrib>Lavaud, J.</creatorcontrib><creatorcontrib>Righini, C.</creatorcontrib><creatorcontrib>Vollaire, J.</creatorcontrib><creatorcontrib>Bellard, E.</creatorcontrib><creatorcontrib>Rols, M.P.</creatorcontrib><creatorcontrib>Teissié, J.</creatorcontrib><creatorcontrib>Coll, J.L.</creatorcontrib><creatorcontrib>Golzio, M.</creatorcontrib><title>Electrochemotherapy guided by intraoperative fluorescence imaging for the treatment of inoperable peritoneal micro-metastases</title><title>Journal of controlled release</title><addtitle>J Control Release</addtitle><description>Surgery is often the first therapeutic indication in cancer. Patient survival essentially depends on the completeness of tumor resection. This is a major challenge, particularly in patients with peritoneal carcinomatosis (PC), where tumors are widely disseminated in the large peritoneal cavity. These small tumors can be difficult to visualize and are often positioned in delicate locations, further increasing the risk of producing serious tissue/organ damage during their ablation. We propose an innovative therapeutic approach based on intraoperative fluorescence (IF) guided electrochemotherapy (ECT) for the treatment of peritoneal micro-metastases. ECT combines the effects of tissue electro-permeabilization (EP) with the administration of an antimitotic agent (bleomycin) that has poor permeability across intact membranes. IF significantly improves the detection of small tumor lesions. ECT is clinically validated for the treatment of cutaneous tumors in animals and humans, but this is the first time that it has been used along with IF imaging for the targeted treatment of peritoneal metastases in a preclinical model.
We set up a murine model of PC that develops secondarily to the resection of a distant primary tumor. Tumor growth and metastasis were finely monitored by non-invasive multimodal imaging (bioluminescence and 3D fluorescence/microCT). Once metastases were detected, mice were randomized into three groups: the ECT group (bleomycin injected intravenously followed by EP) and 2 control groups (bleomycin alone and EP alone). Twenty four hours after the intravenous injection of the tumor targeting agent Angiostamp™700, mice in all groups underwent an abdominal surgery for metastases exploration assisted by fluorescence imaging with the Fluobeam®700 portative device. EP was applied to every nodule detected by IF, except in the bleomycin control group. After surgery, the metastatic invasion was tracked by bioluminescence imaging. In mice treated with bleomycin or EP alone, the metastatic load progressed very rapidly and mice showed no significant difference in lifespan compared to non-operated mice (median lifespan: 27days vs. 25days, respectively). In contrast, the mice treated with ECT displayed a decreased metastatic load and an increased survival rate (median lifespan: 34days). These results provide evidence that IF guided ECT is an effective approach for the treatment of inoperable intraperitoneal micro-metastases.
In this study, we show the effectiveness of an innovative approach of electrochemotherapy guided by intraoperative fluorescence imaging for the treatment of inoperable peritoneal micro-metastases in a preclinical model. [Display omitted]</description><subject>Animals</subject><subject>Antibiotics, Antineoplastic - administration & dosage</subject><subject>Antibiotics, Antineoplastic - therapeutic use</subject><subject>Bleomycin - administration & dosage</subject><subject>Bleomycin - therapeutic use</subject><subject>Cancer</subject><subject>Cell Line, Tumor</subject><subject>Electrochemotherapy</subject><subject>Electroporation</subject><subject>Female</subject><subject>Fluorescence guided surgery</subject><subject>Kidney Neoplasms - diagnostic imaging</subject><subject>Kidney Neoplasms - drug therapy</subject><subject>Kidney Neoplasms - pathology</subject><subject>Life Sciences</subject><subject>Mice, Inbred BALB C</subject><subject>Optical Imaging</subject><subject>Peritoneal metastases</subject><subject>Peritoneal Neoplasms - diagnostic imaging</subject><subject>Peritoneal Neoplasms - drug therapy</subject><subject>Peritoneal Neoplasms - secondary</subject><subject>Tumor targeting</subject><subject>X-Ray Microtomography</subject><issn>0168-3659</issn><issn>1873-4995</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU2P0zAQhi0EYsvCTwD5CIcEf8Sxc0Kr1cIiVeICZ8uxJ62rJC62U6kH_jsOLXtdydLIM8_rGc-L0HtKakpo-_lQH2yYI4w1K9eaiJoQ_gJtqJK8arpOvESbUlAVb0V3g96kdCCECN7I1-iGSSpEKWzQn4cRbI7B7mEKeQ_RHM94t3gHDvdn7OccTTiWdPYnwMO4hAjJwmwB-8ns_LzDQ4i4KHGOYPIEc8ZhKMJ_qn4EXKLPYQYz4snbGKoJsknlQHqLXg1mTPDuGm_Rr68PP-8fq-2Pb9_v77aVbWSXKzlwJXtginHZUinAkV5Ba2SjrASjuLKdaxx3SjFCrKOCdcSAk-XGBiL5Lfp0eXdvRn2MZfJ41sF4_Xi31WuOMN4RJfiJFvbjhT3G8HuBlPXky4_H0cwQlqSpIkoytu7yWVR2irVNYQsqLmhZQEoRhqcxKNGrofqgr4bq1VBNhC6yovtwbbH0E7gn1X8HC_DlAkDZ38lD1Mn61R_nY3FWu-CfafEX8G21_Q</recordid><startdate>20160710</startdate><enddate>20160710</enddate><creator>Josserand, V.</creator><creator>Kéramidas, M.</creator><creator>Lavaud, J.</creator><creator>Righini, C.</creator><creator>Vollaire, J.</creator><creator>Bellard, E.</creator><creator>Rols, M.P.</creator><creator>Teissié, J.</creator><creator>Coll, J.L.</creator><creator>Golzio, M.</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>1XC</scope><scope>VOOES</scope><orcidid>https://orcid.org/0000-0002-7470-3708</orcidid><orcidid>https://orcid.org/0009-0000-6055-8119</orcidid><orcidid>https://orcid.org/0000-0003-3100-6272</orcidid><orcidid>https://orcid.org/0000-0002-7588-8062</orcidid></search><sort><creationdate>20160710</creationdate><title>Electrochemotherapy guided by intraoperative fluorescence imaging for the treatment of inoperable peritoneal micro-metastases</title><author>Josserand, V. ; Kéramidas, M. ; Lavaud, J. ; Righini, C. ; Vollaire, J. ; Bellard, E. ; Rols, M.P. ; Teissié, J. ; Coll, J.L. ; Golzio, M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c479t-7f387be282376175ed0b8e6a748c7ea838c9d4d3d88200cd15290aed72002f073</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animals</topic><topic>Antibiotics, Antineoplastic - administration & dosage</topic><topic>Antibiotics, Antineoplastic - therapeutic use</topic><topic>Bleomycin - administration & dosage</topic><topic>Bleomycin - therapeutic use</topic><topic>Cancer</topic><topic>Cell Line, Tumor</topic><topic>Electrochemotherapy</topic><topic>Electroporation</topic><topic>Female</topic><topic>Fluorescence guided surgery</topic><topic>Kidney Neoplasms - diagnostic imaging</topic><topic>Kidney Neoplasms - drug therapy</topic><topic>Kidney Neoplasms - pathology</topic><topic>Life Sciences</topic><topic>Mice, Inbred BALB C</topic><topic>Optical Imaging</topic><topic>Peritoneal metastases</topic><topic>Peritoneal Neoplasms - diagnostic imaging</topic><topic>Peritoneal Neoplasms - drug therapy</topic><topic>Peritoneal Neoplasms - secondary</topic><topic>Tumor targeting</topic><topic>X-Ray Microtomography</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Josserand, V.</creatorcontrib><creatorcontrib>Kéramidas, M.</creatorcontrib><creatorcontrib>Lavaud, J.</creatorcontrib><creatorcontrib>Righini, C.</creatorcontrib><creatorcontrib>Vollaire, J.</creatorcontrib><creatorcontrib>Bellard, E.</creatorcontrib><creatorcontrib>Rols, M.P.</creatorcontrib><creatorcontrib>Teissié, J.</creatorcontrib><creatorcontrib>Coll, J.L.</creatorcontrib><creatorcontrib>Golzio, M.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>Journal of controlled release</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Josserand, V.</au><au>Kéramidas, M.</au><au>Lavaud, J.</au><au>Righini, C.</au><au>Vollaire, J.</au><au>Bellard, E.</au><au>Rols, M.P.</au><au>Teissié, J.</au><au>Coll, J.L.</au><au>Golzio, M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Electrochemotherapy guided by intraoperative fluorescence imaging for the treatment of inoperable peritoneal micro-metastases</atitle><jtitle>Journal of controlled release</jtitle><addtitle>J Control Release</addtitle><date>2016-07-10</date><risdate>2016</risdate><volume>233</volume><spage>81</spage><epage>87</epage><pages>81-87</pages><issn>0168-3659</issn><eissn>1873-4995</eissn><abstract>Surgery is often the first therapeutic indication in cancer. Patient survival essentially depends on the completeness of tumor resection. This is a major challenge, particularly in patients with peritoneal carcinomatosis (PC), where tumors are widely disseminated in the large peritoneal cavity. These small tumors can be difficult to visualize and are often positioned in delicate locations, further increasing the risk of producing serious tissue/organ damage during their ablation. We propose an innovative therapeutic approach based on intraoperative fluorescence (IF) guided electrochemotherapy (ECT) for the treatment of peritoneal micro-metastases. ECT combines the effects of tissue electro-permeabilization (EP) with the administration of an antimitotic agent (bleomycin) that has poor permeability across intact membranes. IF significantly improves the detection of small tumor lesions. ECT is clinically validated for the treatment of cutaneous tumors in animals and humans, but this is the first time that it has been used along with IF imaging for the targeted treatment of peritoneal metastases in a preclinical model.
We set up a murine model of PC that develops secondarily to the resection of a distant primary tumor. Tumor growth and metastasis were finely monitored by non-invasive multimodal imaging (bioluminescence and 3D fluorescence/microCT). Once metastases were detected, mice were randomized into three groups: the ECT group (bleomycin injected intravenously followed by EP) and 2 control groups (bleomycin alone and EP alone). Twenty four hours after the intravenous injection of the tumor targeting agent Angiostamp™700, mice in all groups underwent an abdominal surgery for metastases exploration assisted by fluorescence imaging with the Fluobeam®700 portative device. EP was applied to every nodule detected by IF, except in the bleomycin control group. After surgery, the metastatic invasion was tracked by bioluminescence imaging. In mice treated with bleomycin or EP alone, the metastatic load progressed very rapidly and mice showed no significant difference in lifespan compared to non-operated mice (median lifespan: 27days vs. 25days, respectively). In contrast, the mice treated with ECT displayed a decreased metastatic load and an increased survival rate (median lifespan: 34days). These results provide evidence that IF guided ECT is an effective approach for the treatment of inoperable intraperitoneal micro-metastases.
In this study, we show the effectiveness of an innovative approach of electrochemotherapy guided by intraoperative fluorescence imaging for the treatment of inoperable peritoneal micro-metastases in a preclinical model. [Display omitted]</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>27155365</pmid><doi>10.1016/j.jconrel.2016.05.003</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-7470-3708</orcidid><orcidid>https://orcid.org/0009-0000-6055-8119</orcidid><orcidid>https://orcid.org/0000-0003-3100-6272</orcidid><orcidid>https://orcid.org/0000-0002-7588-8062</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animals Antibiotics, Antineoplastic - administration & dosage Antibiotics, Antineoplastic - therapeutic use Bleomycin - administration & dosage Bleomycin - therapeutic use Cancer Cell Line, Tumor Electrochemotherapy Electroporation Female Fluorescence guided surgery Kidney Neoplasms - diagnostic imaging Kidney Neoplasms - drug therapy Kidney Neoplasms - pathology Life Sciences Mice, Inbred BALB C Optical Imaging Peritoneal metastases Peritoneal Neoplasms - diagnostic imaging Peritoneal Neoplasms - drug therapy Peritoneal Neoplasms - secondary Tumor targeting X-Ray Microtomography |
title | Electrochemotherapy guided by intraoperative fluorescence imaging for the treatment of inoperable peritoneal micro-metastases |
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