Intraperitoneal immunotherapy: historical perspectives and modern therapy

Intraperitoneal immunotherapy represents a novel strategy for the management of peritoneal metastases (PM). Cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC) has remained the gold standard of treatment for patients with PM, yet despite optimal treatment, recurrence ra...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Cancer gene therapy 2016-11, Vol.23 (11), p.373-381
Hauptverfasser: Morano, W F, Aggarwal, A, Love, P, Richard, S D, Esquivel, J, Bowne, W B
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 381
container_issue 11
container_start_page 373
container_title Cancer gene therapy
container_volume 23
creator Morano, W F
Aggarwal, A
Love, P
Richard, S D
Esquivel, J
Bowne, W B
description Intraperitoneal immunotherapy represents a novel strategy for the management of peritoneal metastases (PM). Cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC) has remained the gold standard of treatment for patients with PM, yet despite optimal treatment, recurrence rates remain high and long-term survival poor. From Coley’s toxins to immune checkpoint inhibitors, the wide variety of anticancer immunotherapeutic strategies are now garnering attention for control of regional disease of the peritoneal cavity. Early studies with vaccine-based therapies, adoptive cell transfer, immune checkpoint inhibitors, and chimeric T cells with tumor-specific antigen receptors (CAR-T cells) are being performed, showing promise for control of peritoneal spread and induction of lasting anticancer immunity. In addition, catumaxomab, a trifunctional antibody, has been approved for intraperitoneal immunotherapy in Europe for the control of malignant ascites in patients with epithelial cell adhesion molecule positive cancers. We review a brief history of immunotherapy and current modalities under investigation for intraperitoneal use in the treatment of PM.
doi_str_mv 10.1038/cgt.2016.49
format Article
fullrecord <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_1846393818</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A470451260</galeid><sourcerecordid>A470451260</sourcerecordid><originalsourceid>FETCH-LOGICAL-c616t-9f77249a1ad48d94e503d9e7c2b67370bbe7ff1469af1473cc1cac08a31936d83</originalsourceid><addsrcrecordid>eNqN0s1rFDEUAPAgil2rJ-8yIIigs-Zr8uGtFLULBS96DtlMZjdlJlmTjND_3rfsVttSigQSyPslj5c8hF4TvCSYqU9uU5cUE7Hk-glaEC5F23UYP0ULrKluicbsBL0o5QpjCEr2HJ1QqRhnnVqg1SrWbHc-h5qit2MTpmmOqW497F5_brah1JSDgwigsvOuht--NDb2zZR6n2NztC_Rs8GOxb86rqfo59cvP84v2svv31bnZ5etE0TUVg9SUq4tsT1Xvea-w6zXXjq6FpJJvF57OQyEC21hlsw54qzDyjKimegVO0XvD_fucvo1-1LNFIrz42ijT3MxRHHBNFPkfyjThFLOGNC39-hVmnOEQgwVnEgqMbhHFKTFikNu9U9t7OhNiEOCJ3b71OaMS8w7QgUGtXxAwej9FBx8xhBg_86Bd7cObOGz6rakca4hxXIXfjhAl1Mp2Q9ml8Nk87Uh2OxbxkDLmH3LGK5BvznWNK8n3_-1Nz0C4OMBFAjFjc-3in7gvj9KlMcN</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1840848468</pqid></control><display><type>article</type><title>Intraperitoneal immunotherapy: historical perspectives and modern therapy</title><source>MEDLINE</source><source>SpringerLink Journals</source><creator>Morano, W F ; Aggarwal, A ; Love, P ; Richard, S D ; Esquivel, J ; Bowne, W B</creator><creatorcontrib>Morano, W F ; Aggarwal, A ; Love, P ; Richard, S D ; Esquivel, J ; Bowne, W B</creatorcontrib><description>Intraperitoneal immunotherapy represents a novel strategy for the management of peritoneal metastases (PM). Cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC) has remained the gold standard of treatment for patients with PM, yet despite optimal treatment, recurrence rates remain high and long-term survival poor. From Coley’s toxins to immune checkpoint inhibitors, the wide variety of anticancer immunotherapeutic strategies are now garnering attention for control of regional disease of the peritoneal cavity. Early studies with vaccine-based therapies, adoptive cell transfer, immune checkpoint inhibitors, and chimeric T cells with tumor-specific antigen receptors (CAR-T cells) are being performed, showing promise for control of peritoneal spread and induction of lasting anticancer immunity. In addition, catumaxomab, a trifunctional antibody, has been approved for intraperitoneal immunotherapy in Europe for the control of malignant ascites in patients with epithelial cell adhesion molecule positive cancers. We review a brief history of immunotherapy and current modalities under investigation for intraperitoneal use in the treatment of PM.</description><identifier>ISSN: 0929-1903</identifier><identifier>EISSN: 1476-5500</identifier><identifier>DOI: 10.1038/cgt.2016.49</identifier><identifier>PMID: 27834358</identifier><language>eng</language><publisher>New York: Nature Publishing Group US</publisher><subject>631/250/251 ; 631/67/1059 ; 631/67/322 ; Animals ; Antibodies, Bispecific - therapeutic use ; Antineoplastic Agents, Immunological - therapeutic use ; Ascites ; Biomedical and Life Sciences ; Biomedicine ; Cancer ; Care and treatment ; Cell adhesion molecules ; Chemotherapy ; Debulking ; Epithelial cells ; Gene Expression ; Gene Therapy ; History, 20th Century ; History, 21st Century ; Humans ; Hyperthermic intraperitoneal chemotherapy ; Immune checkpoint inhibitors ; Immunotherapy ; Immunotherapy - history ; Lymphocytes T ; Metastases ; Patients ; Peritoneal diseases ; Peritoneal Neoplasms - secondary ; Peritoneal Neoplasms - therapy ; Peritoneum ; review</subject><ispartof>Cancer gene therapy, 2016-11, Vol.23 (11), p.373-381</ispartof><rights>Nature America, Inc., part of Springer Nature. 2016</rights><rights>COPYRIGHT 2016 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Nov 2016</rights><rights>Nature America, Inc., part of Springer Nature. 2016.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c616t-9f77249a1ad48d94e503d9e7c2b67370bbe7ff1469af1473cc1cac08a31936d83</citedby><cites>FETCH-LOGICAL-c616t-9f77249a1ad48d94e503d9e7c2b67370bbe7ff1469af1473cc1cac08a31936d83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/cgt.2016.49$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/cgt.2016.49$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27834358$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Morano, W F</creatorcontrib><creatorcontrib>Aggarwal, A</creatorcontrib><creatorcontrib>Love, P</creatorcontrib><creatorcontrib>Richard, S D</creatorcontrib><creatorcontrib>Esquivel, J</creatorcontrib><creatorcontrib>Bowne, W B</creatorcontrib><title>Intraperitoneal immunotherapy: historical perspectives and modern therapy</title><title>Cancer gene therapy</title><addtitle>Cancer Gene Ther</addtitle><addtitle>Cancer Gene Ther</addtitle><description>Intraperitoneal immunotherapy represents a novel strategy for the management of peritoneal metastases (PM). Cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC) has remained the gold standard of treatment for patients with PM, yet despite optimal treatment, recurrence rates remain high and long-term survival poor. From Coley’s toxins to immune checkpoint inhibitors, the wide variety of anticancer immunotherapeutic strategies are now garnering attention for control of regional disease of the peritoneal cavity. Early studies with vaccine-based therapies, adoptive cell transfer, immune checkpoint inhibitors, and chimeric T cells with tumor-specific antigen receptors (CAR-T cells) are being performed, showing promise for control of peritoneal spread and induction of lasting anticancer immunity. In addition, catumaxomab, a trifunctional antibody, has been approved for intraperitoneal immunotherapy in Europe for the control of malignant ascites in patients with epithelial cell adhesion molecule positive cancers. We review a brief history of immunotherapy and current modalities under investigation for intraperitoneal use in the treatment of PM.</description><subject>631/250/251</subject><subject>631/67/1059</subject><subject>631/67/322</subject><subject>Animals</subject><subject>Antibodies, Bispecific - therapeutic use</subject><subject>Antineoplastic Agents, Immunological - therapeutic use</subject><subject>Ascites</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cancer</subject><subject>Care and treatment</subject><subject>Cell adhesion molecules</subject><subject>Chemotherapy</subject><subject>Debulking</subject><subject>Epithelial cells</subject><subject>Gene Expression</subject><subject>Gene Therapy</subject><subject>History, 20th Century</subject><subject>History, 21st Century</subject><subject>Humans</subject><subject>Hyperthermic intraperitoneal chemotherapy</subject><subject>Immune checkpoint inhibitors</subject><subject>Immunotherapy</subject><subject>Immunotherapy - history</subject><subject>Lymphocytes T</subject><subject>Metastases</subject><subject>Patients</subject><subject>Peritoneal diseases</subject><subject>Peritoneal Neoplasms - secondary</subject><subject>Peritoneal Neoplasms - therapy</subject><subject>Peritoneum</subject><subject>review</subject><issn>0929-1903</issn><issn>1476-5500</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqN0s1rFDEUAPAgil2rJ-8yIIigs-Zr8uGtFLULBS96DtlMZjdlJlmTjND_3rfsVttSigQSyPslj5c8hF4TvCSYqU9uU5cUE7Hk-glaEC5F23UYP0ULrKluicbsBL0o5QpjCEr2HJ1QqRhnnVqg1SrWbHc-h5qit2MTpmmOqW497F5_brah1JSDgwigsvOuht--NDb2zZR6n2NztC_Rs8GOxb86rqfo59cvP84v2svv31bnZ5etE0TUVg9SUq4tsT1Xvea-w6zXXjq6FpJJvF57OQyEC21hlsw54qzDyjKimegVO0XvD_fucvo1-1LNFIrz42ijT3MxRHHBNFPkfyjThFLOGNC39-hVmnOEQgwVnEgqMbhHFKTFikNu9U9t7OhNiEOCJ3b71OaMS8w7QgUGtXxAwej9FBx8xhBg_86Bd7cObOGz6rakca4hxXIXfjhAl1Mp2Q9ml8Nk87Uh2OxbxkDLmH3LGK5BvznWNK8n3_-1Nz0C4OMBFAjFjc-3in7gvj9KlMcN</recordid><startdate>20161101</startdate><enddate>20161101</enddate><creator>Morano, W F</creator><creator>Aggarwal, A</creator><creator>Love, P</creator><creator>Richard, S D</creator><creator>Esquivel, J</creator><creator>Bowne, W B</creator><general>Nature Publishing Group US</general><general>Nature Publishing Group</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>3V.</scope><scope>7QP</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>7X8</scope><scope>7QO</scope><scope>7T5</scope></search><sort><creationdate>20161101</creationdate><title>Intraperitoneal immunotherapy: historical perspectives and modern therapy</title><author>Morano, W F ; Aggarwal, A ; Love, P ; Richard, S D ; Esquivel, J ; Bowne, W B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c616t-9f77249a1ad48d94e503d9e7c2b67370bbe7ff1469af1473cc1cac08a31936d83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>631/250/251</topic><topic>631/67/1059</topic><topic>631/67/322</topic><topic>Animals</topic><topic>Antibodies, Bispecific - therapeutic use</topic><topic>Antineoplastic Agents, Immunological - therapeutic use</topic><topic>Ascites</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cancer</topic><topic>Care and treatment</topic><topic>Cell adhesion molecules</topic><topic>Chemotherapy</topic><topic>Debulking</topic><topic>Epithelial cells</topic><topic>Gene Expression</topic><topic>Gene Therapy</topic><topic>History, 20th Century</topic><topic>History, 21st Century</topic><topic>Humans</topic><topic>Hyperthermic intraperitoneal chemotherapy</topic><topic>Immune checkpoint inhibitors</topic><topic>Immunotherapy</topic><topic>Immunotherapy - history</topic><topic>Lymphocytes T</topic><topic>Metastases</topic><topic>Patients</topic><topic>Peritoneal diseases</topic><topic>Peritoneal Neoplasms - secondary</topic><topic>Peritoneal Neoplasms - therapy</topic><topic>Peritoneum</topic><topic>review</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Morano, W F</creatorcontrib><creatorcontrib>Aggarwal, A</creatorcontrib><creatorcontrib>Love, P</creatorcontrib><creatorcontrib>Richard, S D</creatorcontrib><creatorcontrib>Esquivel, J</creatorcontrib><creatorcontrib>Bowne, W B</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Biotechnology Research Abstracts</collection><collection>Immunology Abstracts</collection><jtitle>Cancer gene therapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Morano, W F</au><au>Aggarwal, A</au><au>Love, P</au><au>Richard, S D</au><au>Esquivel, J</au><au>Bowne, W B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intraperitoneal immunotherapy: historical perspectives and modern therapy</atitle><jtitle>Cancer gene therapy</jtitle><stitle>Cancer Gene Ther</stitle><addtitle>Cancer Gene Ther</addtitle><date>2016-11-01</date><risdate>2016</risdate><volume>23</volume><issue>11</issue><spage>373</spage><epage>381</epage><pages>373-381</pages><issn>0929-1903</issn><eissn>1476-5500</eissn><abstract>Intraperitoneal immunotherapy represents a novel strategy for the management of peritoneal metastases (PM). Cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC) has remained the gold standard of treatment for patients with PM, yet despite optimal treatment, recurrence rates remain high and long-term survival poor. From Coley’s toxins to immune checkpoint inhibitors, the wide variety of anticancer immunotherapeutic strategies are now garnering attention for control of regional disease of the peritoneal cavity. Early studies with vaccine-based therapies, adoptive cell transfer, immune checkpoint inhibitors, and chimeric T cells with tumor-specific antigen receptors (CAR-T cells) are being performed, showing promise for control of peritoneal spread and induction of lasting anticancer immunity. In addition, catumaxomab, a trifunctional antibody, has been approved for intraperitoneal immunotherapy in Europe for the control of malignant ascites in patients with epithelial cell adhesion molecule positive cancers. We review a brief history of immunotherapy and current modalities under investigation for intraperitoneal use in the treatment of PM.</abstract><cop>New York</cop><pub>Nature Publishing Group US</pub><pmid>27834358</pmid><doi>10.1038/cgt.2016.49</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0929-1903
ispartof Cancer gene therapy, 2016-11, Vol.23 (11), p.373-381
issn 0929-1903
1476-5500
language eng
recordid cdi_proquest_miscellaneous_1846393818
source MEDLINE; SpringerLink Journals
subjects 631/250/251
631/67/1059
631/67/322
Animals
Antibodies, Bispecific - therapeutic use
Antineoplastic Agents, Immunological - therapeutic use
Ascites
Biomedical and Life Sciences
Biomedicine
Cancer
Care and treatment
Cell adhesion molecules
Chemotherapy
Debulking
Epithelial cells
Gene Expression
Gene Therapy
History, 20th Century
History, 21st Century
Humans
Hyperthermic intraperitoneal chemotherapy
Immune checkpoint inhibitors
Immunotherapy
Immunotherapy - history
Lymphocytes T
Metastases
Patients
Peritoneal diseases
Peritoneal Neoplasms - secondary
Peritoneal Neoplasms - therapy
Peritoneum
review
title Intraperitoneal immunotherapy: historical perspectives and modern therapy
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-04T01%3A33%3A14IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Intraperitoneal%20immunotherapy:%20historical%20perspectives%20and%20modern%20therapy&rft.jtitle=Cancer%20gene%20therapy&rft.au=Morano,%20W%20F&rft.date=2016-11-01&rft.volume=23&rft.issue=11&rft.spage=373&rft.epage=381&rft.pages=373-381&rft.issn=0929-1903&rft.eissn=1476-5500&rft_id=info:doi/10.1038/cgt.2016.49&rft_dat=%3Cgale_proqu%3EA470451260%3C/gale_proqu%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1840848468&rft_id=info:pmid/27834358&rft_galeid=A470451260&rfr_iscdi=true