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...
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Veröffentlicht in: | Cancer 1989-05, Vol.63 (10), p.1998-2004 |
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container_end_page | 2004 |
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container_issue | 10 |
container_start_page | 1998 |
container_title | Cancer |
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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 |
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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. 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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. 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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<1998::AID-CNCR2820631022>3.0.CO;2-L</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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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 |
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