Recombinant interferon‐γ lacks activity against metastatic colorectal cancer but increases serum levels of ca 19‐9

A clinical trial to determine the antitumor activity of recombinant interferon‐gamma (rIFN‐γ) was conducted in 36 patients with advanced colorectal cancer. Severe constitutional symptoms were seen in the first five patients who received rIFN‐γ as a 2‐ to 4‐hour intravenous infusion, and this method...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Cancer 1989-05, Vol.63 (10), p.1998-2004
Hauptverfasser: O'Connell, Michael J., Ritts, Roy A., Moertel, Charles G., Schutt, Allan J., Sherwin, Stephen A.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 2004
container_issue 10
container_start_page 1998
container_title Cancer
container_volume 63
creator O'Connell, Michael J.
Ritts, Roy A.
Moertel, Charles G.
Schutt, Allan J.
Sherwin, Stephen A.
description A clinical trial to determine the antitumor activity of recombinant interferon‐gamma (rIFN‐γ) was conducted in 36 patients with advanced colorectal cancer. Severe constitutional symptoms were seen in the first five patients who received rIFN‐γ as a 2‐ to 4‐hour intravenous infusion, and this method of administration was therefore abandoned. One transient partial tumor regression was observed in the 31 patients who received treatment by the intramuscular route of administration. Although a clinically tolerable regimen suitable for outpatient administration was developed, rIFN‐γ given in this dose and schedule had minimal antitumor effect for the treatment of advanced colorectal cancer. NK activity was depressed within 48 hours of rIFN‐γ administration but became significantly higher than normal controls or pretreatment levels during therapy despite disease progression, indicating discordance between augmentation of this immune parameter and tumor status. Serum CA 19‐9 levels were unusually high and increased significantly more than CA 125 or CEA during rIFN‐γ treatment. This observation suggests that rIFN‐γ could augment localization of anti‐CA 19‐9 used to diagnostically image or therapeutically target a labeled chemotherapy agent to tumor in those patients expressing this antigen.
doi_str_mv 10.1002/1097-0142(19890515)63:10<1998::AID-CNCR2820631022>3.0.CO;2-L
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_78886673</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>78886673</sourcerecordid><originalsourceid>FETCH-LOGICAL-c5012-eee0f47308a9deb4ba114df09314c61c99ad545da74ebe8cb72d370ad834b1873</originalsourceid><addsrcrecordid>eNqVkd9qFDEYxYModVt9BCEXIvZi1vybSbIVoUz9U1hcKApeCCGT-aaMZmZqkmnZOx_Bd_E9fAifxNnuuqAXglchnPMdDueH0Bklc0oIe0aJlhmhgj2lWmmS0_y44AtKnlOt1WJxen6WlW_LC6YYKTgljL3gczIvVycsW95Bs_35XTQjhKgsF_zDfXQY46fpK1nOD9ABk0pISmfo5gLc0FVtb_uE2z5BaCAM_c-v3358x966zxFbl9rrNq2xvbRtHxPuINmYbGoddoMfArhkPXa2dxBwNW5yXAAbIeIIYeywh2vwEQ_NZMJUT-H6AbrXWB_h4e49Qu9fvXxXvsmWq9fn5ekyczmhLAMA0gjJibK6hkpUllJRN0RzKlxBnda2zkVeWymgAuUqyWouia0VFxVVkh-hJ9vcqzB8GSEm07XRgfe2h2GMRiqlikLyyfhxa3RhiDFAY65C29mwNpSYDRezGdZshjW_uZiC36oTF2MmLuZPLoYbYsqVYWY5xT_a9RirDup9-A7EpD_e6TY665swrdnGva1QjPHblpdb203rYf2fFf_Z8C-F_wLE0rwo</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>78886673</pqid></control><display><type>article</type><title>Recombinant interferon‐γ lacks activity against metastatic colorectal cancer but increases serum levels of ca 19‐9</title><source>MEDLINE</source><source>Alma/SFX Local Collection</source><creator>O'Connell, Michael J. ; Ritts, Roy A. ; Moertel, Charles G. ; Schutt, Allan J. ; Sherwin, Stephen A.</creator><creatorcontrib>O'Connell, Michael J. ; Ritts, Roy A. ; Moertel, Charles G. ; Schutt, Allan J. ; Sherwin, Stephen A.</creatorcontrib><description>A clinical trial to determine the antitumor activity of recombinant interferon‐gamma (rIFN‐γ) was conducted in 36 patients with advanced colorectal cancer. Severe constitutional symptoms were seen in the first five patients who received rIFN‐γ as a 2‐ to 4‐hour intravenous infusion, and this method of administration was therefore abandoned. One transient partial tumor regression was observed in the 31 patients who received treatment by the intramuscular route of administration. Although a clinically tolerable regimen suitable for outpatient administration was developed, rIFN‐γ given in this dose and schedule had minimal antitumor effect for the treatment of advanced colorectal cancer. NK activity was depressed within 48 hours of rIFN‐γ administration but became significantly higher than normal controls or pretreatment levels during therapy despite disease progression, indicating discordance between augmentation of this immune parameter and tumor status. Serum CA 19‐9 levels were unusually high and increased significantly more than CA 125 or CEA during rIFN‐γ treatment. This observation suggests that rIFN‐γ could augment localization of anti‐CA 19‐9 used to diagnostically image or therapeutically target a labeled chemotherapy agent to tumor in those patients expressing this antigen.</description><identifier>ISSN: 0008-543X</identifier><identifier>EISSN: 1097-0142</identifier><identifier>DOI: 10.1002/1097-0142(19890515)63:10&lt;1998::AID-CNCR2820631022&gt;3.0.CO;2-L</identifier><identifier>PMID: 2784711</identifier><identifier>CODEN: CANCAR</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adult ; Aged ; Antigens, Tumor-Associated, Carbohydrate - metabolism ; Antineoplastic agents ; Aspartate Aminotransferases - blood ; Biological and medical sciences ; Carcinoembryonic Antigen - metabolism ; Chemotherapy ; Colorectal Neoplasms - blood ; Colorectal Neoplasms - immunology ; Colorectal Neoplasms - therapy ; Female ; Humans ; Interferon Type I - adverse effects ; Interferon Type I - therapeutic use ; Killer Cells, Natural - cytology ; Male ; Medical sciences ; Middle Aged ; Pharmacology. Drug treatments ; T-Lymphocytes - classification</subject><ispartof>Cancer, 1989-05, Vol.63 (10), p.1998-2004</ispartof><rights>Copyright © 1989 American Cancer Society</rights><rights>1990 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c5012-eee0f47308a9deb4ba114df09314c61c99ad545da74ebe8cb72d370ad834b1873</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27915,27916</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=6822373$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2784711$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>O'Connell, Michael J.</creatorcontrib><creatorcontrib>Ritts, Roy A.</creatorcontrib><creatorcontrib>Moertel, Charles G.</creatorcontrib><creatorcontrib>Schutt, Allan J.</creatorcontrib><creatorcontrib>Sherwin, Stephen A.</creatorcontrib><title>Recombinant interferon‐γ lacks activity against metastatic colorectal cancer but increases serum levels of ca 19‐9</title><title>Cancer</title><addtitle>Cancer</addtitle><description>A clinical trial to determine the antitumor activity of recombinant interferon‐gamma (rIFN‐γ) was conducted in 36 patients with advanced colorectal cancer. Severe constitutional symptoms were seen in the first five patients who received rIFN‐γ as a 2‐ to 4‐hour intravenous infusion, and this method of administration was therefore abandoned. One transient partial tumor regression was observed in the 31 patients who received treatment by the intramuscular route of administration. Although a clinically tolerable regimen suitable for outpatient administration was developed, rIFN‐γ given in this dose and schedule had minimal antitumor effect for the treatment of advanced colorectal cancer. NK activity was depressed within 48 hours of rIFN‐γ administration but became significantly higher than normal controls or pretreatment levels during therapy despite disease progression, indicating discordance between augmentation of this immune parameter and tumor status. Serum CA 19‐9 levels were unusually high and increased significantly more than CA 125 or CEA during rIFN‐γ treatment. This observation suggests that rIFN‐γ could augment localization of anti‐CA 19‐9 used to diagnostically image or therapeutically target a labeled chemotherapy agent to tumor in those patients expressing this antigen.</description><subject>Adult</subject><subject>Aged</subject><subject>Antigens, Tumor-Associated, Carbohydrate - metabolism</subject><subject>Antineoplastic agents</subject><subject>Aspartate Aminotransferases - blood</subject><subject>Biological and medical sciences</subject><subject>Carcinoembryonic Antigen - metabolism</subject><subject>Chemotherapy</subject><subject>Colorectal Neoplasms - blood</subject><subject>Colorectal Neoplasms - immunology</subject><subject>Colorectal Neoplasms - therapy</subject><subject>Female</subject><subject>Humans</subject><subject>Interferon Type I - adverse effects</subject><subject>Interferon Type I - therapeutic use</subject><subject>Killer Cells, Natural - cytology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Pharmacology. Drug treatments</subject><subject>T-Lymphocytes - classification</subject><issn>0008-543X</issn><issn>1097-0142</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkd9qFDEYxYModVt9BCEXIvZi1vybSbIVoUz9U1hcKApeCCGT-aaMZmZqkmnZOx_Bd_E9fAifxNnuuqAXglchnPMdDueH0Bklc0oIe0aJlhmhgj2lWmmS0_y44AtKnlOt1WJxen6WlW_LC6YYKTgljL3gczIvVycsW95Bs_35XTQjhKgsF_zDfXQY46fpK1nOD9ABk0pISmfo5gLc0FVtb_uE2z5BaCAM_c-v3358x966zxFbl9rrNq2xvbRtHxPuINmYbGoddoMfArhkPXa2dxBwNW5yXAAbIeIIYeywh2vwEQ_NZMJUT-H6AbrXWB_h4e49Qu9fvXxXvsmWq9fn5ekyczmhLAMA0gjJibK6hkpUllJRN0RzKlxBnda2zkVeWymgAuUqyWouia0VFxVVkh-hJ9vcqzB8GSEm07XRgfe2h2GMRiqlikLyyfhxa3RhiDFAY65C29mwNpSYDRezGdZshjW_uZiC36oTF2MmLuZPLoYbYsqVYWY5xT_a9RirDup9-A7EpD_e6TY665swrdnGva1QjPHblpdb203rYf2fFf_Z8C-F_wLE0rwo</recordid><startdate>19890515</startdate><enddate>19890515</enddate><creator>O'Connell, Michael J.</creator><creator>Ritts, Roy A.</creator><creator>Moertel, Charles G.</creator><creator>Schutt, Allan J.</creator><creator>Sherwin, Stephen A.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>IQODW</scope><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></search><sort><creationdate>19890515</creationdate><title>Recombinant interferon‐γ lacks activity against metastatic colorectal cancer but increases serum levels of ca 19‐9</title><author>O'Connell, Michael J. ; Ritts, Roy A. ; Moertel, Charles G. ; Schutt, Allan J. ; Sherwin, Stephen A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5012-eee0f47308a9deb4ba114df09314c61c99ad545da74ebe8cb72d370ad834b1873</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Antigens, Tumor-Associated, Carbohydrate - metabolism</topic><topic>Antineoplastic agents</topic><topic>Aspartate Aminotransferases - blood</topic><topic>Biological and medical sciences</topic><topic>Carcinoembryonic Antigen - metabolism</topic><topic>Chemotherapy</topic><topic>Colorectal Neoplasms - blood</topic><topic>Colorectal Neoplasms - immunology</topic><topic>Colorectal Neoplasms - therapy</topic><topic>Female</topic><topic>Humans</topic><topic>Interferon Type I - adverse effects</topic><topic>Interferon Type I - therapeutic use</topic><topic>Killer Cells, Natural - cytology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Pharmacology. Drug treatments</topic><topic>T-Lymphocytes - classification</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>O'Connell, Michael J.</creatorcontrib><creatorcontrib>Ritts, Roy A.</creatorcontrib><creatorcontrib>Moertel, Charles G.</creatorcontrib><creatorcontrib>Schutt, Allan J.</creatorcontrib><creatorcontrib>Sherwin, Stephen A.</creatorcontrib><collection>Pascal-Francis</collection><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><jtitle>Cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>O'Connell, Michael J.</au><au>Ritts, Roy A.</au><au>Moertel, Charles G.</au><au>Schutt, Allan J.</au><au>Sherwin, Stephen A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Recombinant interferon‐γ lacks activity against metastatic colorectal cancer but increases serum levels of ca 19‐9</atitle><jtitle>Cancer</jtitle><addtitle>Cancer</addtitle><date>1989-05-15</date><risdate>1989</risdate><volume>63</volume><issue>10</issue><spage>1998</spage><epage>2004</epage><pages>1998-2004</pages><issn>0008-543X</issn><eissn>1097-0142</eissn><coden>CANCAR</coden><abstract>A clinical trial to determine the antitumor activity of recombinant interferon‐gamma (rIFN‐γ) was conducted in 36 patients with advanced colorectal cancer. Severe constitutional symptoms were seen in the first five patients who received rIFN‐γ as a 2‐ to 4‐hour intravenous infusion, and this method of administration was therefore abandoned. One transient partial tumor regression was observed in the 31 patients who received treatment by the intramuscular route of administration. Although a clinically tolerable regimen suitable for outpatient administration was developed, rIFN‐γ given in this dose and schedule had minimal antitumor effect for the treatment of advanced colorectal cancer. NK activity was depressed within 48 hours of rIFN‐γ administration but became significantly higher than normal controls or pretreatment levels during therapy despite disease progression, indicating discordance between augmentation of this immune parameter and tumor status. Serum CA 19‐9 levels were unusually high and increased significantly more than CA 125 or CEA during rIFN‐γ treatment. This observation suggests that rIFN‐γ could augment localization of anti‐CA 19‐9 used to diagnostically image or therapeutically target a labeled chemotherapy agent to tumor in those patients expressing this antigen.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>2784711</pmid><doi>10.1002/1097-0142(19890515)63:10&lt;1998::AID-CNCR2820631022&gt;3.0.CO;2-L</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0008-543X
ispartof Cancer, 1989-05, Vol.63 (10), p.1998-2004
issn 0008-543X
1097-0142
language eng
recordid cdi_proquest_miscellaneous_78886673
source MEDLINE; Alma/SFX Local Collection
subjects Adult
Aged
Antigens, Tumor-Associated, Carbohydrate - metabolism
Antineoplastic agents
Aspartate Aminotransferases - blood
Biological and medical sciences
Carcinoembryonic Antigen - metabolism
Chemotherapy
Colorectal Neoplasms - blood
Colorectal Neoplasms - immunology
Colorectal Neoplasms - therapy
Female
Humans
Interferon Type I - adverse effects
Interferon Type I - therapeutic use
Killer Cells, Natural - cytology
Male
Medical sciences
Middle Aged
Pharmacology. Drug treatments
T-Lymphocytes - classification
title Recombinant interferon‐γ lacks activity against metastatic colorectal cancer but increases serum levels of ca 19‐9
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-15T00%3A39%3A59IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Recombinant%20interferon%E2%80%90%CE%B3%20lacks%20activity%20against%20metastatic%20colorectal%20cancer%20but%20increases%20serum%20levels%20of%20ca%2019%E2%80%909&rft.jtitle=Cancer&rft.au=O'Connell,%20Michael%20J.&rft.date=1989-05-15&rft.volume=63&rft.issue=10&rft.spage=1998&rft.epage=2004&rft.pages=1998-2004&rft.issn=0008-543X&rft.eissn=1097-0142&rft.coden=CANCAR&rft_id=info:doi/10.1002/1097-0142(19890515)63:10%3C1998::AID-CNCR2820631022%3E3.0.CO;2-L&rft_dat=%3Cproquest_cross%3E78886673%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=78886673&rft_id=info:pmid/2784711&rfr_iscdi=true