Acute phase proteins and recombinant IL‐2 therapy: prediction of response and survival in patients with colorectal cancer
SUMMARY Twenty‐four patients with metastatic colorectal cancer were treated with recombinant IL‐2 (rIL‐2) by continuous intravenous infusion for 5 days (18 · 106 U/m2 per 24 h), followed by three injections of 5‐fluorouracil (600 mg/m2) and folinic acid (25mg/m2) at weekly intervals. The response to...
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Veröffentlicht in: | Clinical and experimental immunology 1995-02, Vol.99 (2), p.143-147 |
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Twenty‐four patients with metastatic colorectal cancer were treated with recombinant IL‐2 (rIL‐2) by continuous intravenous infusion for 5 days (18 · 106 U/m2 per 24 h), followed by three injections of 5‐fluorouracil (600 mg/m2) and folinic acid (25mg/m2) at weekly intervals. The response to treatment was assessed using standard UICC criteria (partial or complete response, stasis or progression of disease). The serum concentrations of the acute phase proteins; C‐reactive protein (CRP), retinol binding protein (RBP), α1‐antitrypsin (α1‐AT), transferrin (TF) and albumin were measured. A response to therapy occurred in the tumours of seven (29%) of the 24 patients (two complete and five partial responses). All patients who demonstrated a response to treatment had a serum albumin level of > 37 g/l and a CRP level of · 10 mg/l. In contrast, of the 17 patients who did not respond to therapy, 12 (71%) had a serum albumin of less than 37 g/dl and a CRP of greater than 10 mg/l. Examination of the survival times of the 12 patients who had a pretreatment serum albumin level of less than 37 g/l revealed that all had died within 12 months of cessation of therapy. However, 58% of patients with pretreatment serum albumin levels of greater than 37 g/l survived for longer than 12 months. These results have shown that (i) patients who respond to rIL‐2‐based therapy and (ii) those patients who have prolonged survival times, can be identified by pretreatment measurement of serum levels of acute phase proteins. |
doi_str_mv | 10.1111/j.1365-2249.1995.tb05524.x |
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Twenty‐four patients with metastatic colorectal cancer were treated with recombinant IL‐2 (rIL‐2) by continuous intravenous infusion for 5 days (18 · 106 U/m2 per 24 h), followed by three injections of 5‐fluorouracil (600 mg/m2) and folinic acid (25mg/m2) at weekly intervals. The response to treatment was assessed using standard UICC criteria (partial or complete response, stasis or progression of disease). The serum concentrations of the acute phase proteins; C‐reactive protein (CRP), retinol binding protein (RBP), α1‐antitrypsin (α1‐AT), transferrin (TF) and albumin were measured. A response to therapy occurred in the tumours of seven (29%) of the 24 patients (two complete and five partial responses). All patients who demonstrated a response to treatment had a serum albumin level of > 37 g/l and a CRP level of · 10 mg/l. In contrast, of the 17 patients who did not respond to therapy, 12 (71%) had a serum albumin of less than 37 g/dl and a CRP of greater than 10 mg/l. Examination of the survival times of the 12 patients who had a pretreatment serum albumin level of less than 37 g/l revealed that all had died within 12 months of cessation of therapy. However, 58% of patients with pretreatment serum albumin levels of greater than 37 g/l survived for longer than 12 months. These results have shown that (i) patients who respond to rIL‐2‐based therapy and (ii) those patients who have prolonged survival times, can be identified by pretreatment measurement of serum levels of acute phase proteins.</description><identifier>ISSN: 0009-9104</identifier><identifier>EISSN: 1365-2249</identifier><identifier>DOI: 10.1111/j.1365-2249.1995.tb05524.x</identifier><identifier>PMID: 7531626</identifier><identifier>CODEN: CEXIAL</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>acute phase response ; Acute-Phase Proteins - analysis ; Biological and medical sciences ; Biomarkers, Tumor - blood ; Colorectal Neoplasms - blood ; Colorectal Neoplasms - mortality ; Colorectal Neoplasms - therapy ; Combined Modality Therapy ; Fluorouracil - therapeutic use ; Gastroenterology. Liver. Pancreas. Abdomen ; Humans ; IL‐2 therapy ; Interleukin-2 - therapeutic use ; Leucovorin - therapeutic use ; Medical sciences ; Neoplasm Metastasis ; Recombinant Proteins - therapeutic use ; response and survival ; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus ; Survival Analysis ; Tumors</subject><ispartof>Clinical and experimental immunology, 1995-02, Vol.99 (2), p.143-147</ispartof><rights>1995 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5363-aa6d32b5080198a616d21c965d735f35d2a6064959757b9336c42ca557fb74823</citedby><cites>FETCH-LOGICAL-c5363-aa6d32b5080198a616d21c965d735f35d2a6064959757b9336c42ca557fb74823</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1534287/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1534287/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3407543$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7531626$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>SIMPSON, W. G.</creatorcontrib><creatorcontrib>HEYS, S. D.</creatorcontrib><creatorcontrib>WHITING, P. H.</creatorcontrib><creatorcontrib>EREMIN, O.</creatorcontrib><creatorcontrib>BROOM, J.</creatorcontrib><title>Acute phase proteins and recombinant IL‐2 therapy: prediction of response and survival in patients with colorectal cancer</title><title>Clinical and experimental immunology</title><addtitle>Clin Exp Immunol</addtitle><description>SUMMARY
Twenty‐four patients with metastatic colorectal cancer were treated with recombinant IL‐2 (rIL‐2) by continuous intravenous infusion for 5 days (18 · 106 U/m2 per 24 h), followed by three injections of 5‐fluorouracil (600 mg/m2) and folinic acid (25mg/m2) at weekly intervals. The response to treatment was assessed using standard UICC criteria (partial or complete response, stasis or progression of disease). The serum concentrations of the acute phase proteins; C‐reactive protein (CRP), retinol binding protein (RBP), α1‐antitrypsin (α1‐AT), transferrin (TF) and albumin were measured. A response to therapy occurred in the tumours of seven (29%) of the 24 patients (two complete and five partial responses). All patients who demonstrated a response to treatment had a serum albumin level of > 37 g/l and a CRP level of · 10 mg/l. In contrast, of the 17 patients who did not respond to therapy, 12 (71%) had a serum albumin of less than 37 g/dl and a CRP of greater than 10 mg/l. Examination of the survival times of the 12 patients who had a pretreatment serum albumin level of less than 37 g/l revealed that all had died within 12 months of cessation of therapy. However, 58% of patients with pretreatment serum albumin levels of greater than 37 g/l survived for longer than 12 months. These results have shown that (i) patients who respond to rIL‐2‐based therapy and (ii) those patients who have prolonged survival times, can be identified by pretreatment measurement of serum levels of acute phase proteins.</description><subject>acute phase response</subject><subject>Acute-Phase Proteins - analysis</subject><subject>Biological and medical sciences</subject><subject>Biomarkers, Tumor - blood</subject><subject>Colorectal Neoplasms - blood</subject><subject>Colorectal Neoplasms - mortality</subject><subject>Colorectal Neoplasms - therapy</subject><subject>Combined Modality Therapy</subject><subject>Fluorouracil - therapeutic use</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Humans</subject><subject>IL‐2 therapy</subject><subject>Interleukin-2 - therapeutic use</subject><subject>Leucovorin - therapeutic use</subject><subject>Medical sciences</subject><subject>Neoplasm Metastasis</subject><subject>Recombinant Proteins - therapeutic use</subject><subject>response and survival</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</subject><subject>Survival Analysis</subject><subject>Tumors</subject><issn>0009-9104</issn><issn>1365-2249</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVUd2K1DAYDaKs4-ojCEVk71rz0yTNXgjLsOrAgDd6HdI0dTJ0kpqkszt44yP4jD6JKVtGvRJzkfBxfjj5DgCvEKxQPm_2FSKMlhjXokJC0Cq1kFJcV_ePwOoMPQYrCKEoBYL1U_Asxn0eGWP4AlxwShDDbAW-3egpmWLcqZjv4JOxLhbKdUUw2h9a65RLxWb78_sPXKSdCWo8XWei6axO1rvC95kZR--yfpbFKRztUQ2FdcWokjUuxeLOpl2h_eCzacqYVk6b8Bw86dUQzYvlvQSf391-Wn8otx_fb9Y321JTwkipFOsIbilsIBKNYoh1GGnBaMcJ7QntsGKQ1YIKTnkrCGG6xlpRyvuW1w0ml-Dtg-84tQfT6RwpqEGOwR5UOEmvrPwbcXYnv_ijRJTUuOHZ4GoxCP7rZGKSBxu1GQbljJ-i5BzVjFH2TyJiDRZ59Zl4_UDUwccYTH9Og6CcO5Z7ORcp5yLl3LFcOpb3Wfzyz_-cpUupGX-94CpqNfQhb9vGM43UkNOa_F7LnR3M6T8CyPXtBmWDXxDtxis</recordid><startdate>199502</startdate><enddate>199502</enddate><creator>SIMPSON, W. G.</creator><creator>HEYS, S. D.</creator><creator>WHITING, P. H.</creator><creator>EREMIN, O.</creator><creator>BROOM, J.</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</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>7T5</scope><scope>H94</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>199502</creationdate><title>Acute phase proteins and recombinant IL‐2 therapy: prediction of response and survival in patients with colorectal cancer</title><author>SIMPSON, W. G. ; HEYS, S. D. ; WHITING, P. H. ; EREMIN, O. ; BROOM, J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5363-aa6d32b5080198a616d21c965d735f35d2a6064959757b9336c42ca557fb74823</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>acute phase response</topic><topic>Acute-Phase Proteins - analysis</topic><topic>Biological and medical sciences</topic><topic>Biomarkers, Tumor - blood</topic><topic>Colorectal Neoplasms - blood</topic><topic>Colorectal Neoplasms - mortality</topic><topic>Colorectal Neoplasms - therapy</topic><topic>Combined Modality Therapy</topic><topic>Fluorouracil - therapeutic use</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Humans</topic><topic>IL‐2 therapy</topic><topic>Interleukin-2 - therapeutic use</topic><topic>Leucovorin - therapeutic use</topic><topic>Medical sciences</topic><topic>Neoplasm Metastasis</topic><topic>Recombinant Proteins - therapeutic use</topic><topic>response and survival</topic><topic>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</topic><topic>Survival Analysis</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SIMPSON, W. G.</creatorcontrib><creatorcontrib>HEYS, S. D.</creatorcontrib><creatorcontrib>WHITING, P. H.</creatorcontrib><creatorcontrib>EREMIN, O.</creatorcontrib><creatorcontrib>BROOM, J.</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>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Clinical and experimental immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SIMPSON, W. G.</au><au>HEYS, S. D.</au><au>WHITING, P. H.</au><au>EREMIN, O.</au><au>BROOM, J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Acute phase proteins and recombinant IL‐2 therapy: prediction of response and survival in patients with colorectal cancer</atitle><jtitle>Clinical and experimental immunology</jtitle><addtitle>Clin Exp Immunol</addtitle><date>1995-02</date><risdate>1995</risdate><volume>99</volume><issue>2</issue><spage>143</spage><epage>147</epage><pages>143-147</pages><issn>0009-9104</issn><eissn>1365-2249</eissn><coden>CEXIAL</coden><abstract>SUMMARY
Twenty‐four patients with metastatic colorectal cancer were treated with recombinant IL‐2 (rIL‐2) by continuous intravenous infusion for 5 days (18 · 106 U/m2 per 24 h), followed by three injections of 5‐fluorouracil (600 mg/m2) and folinic acid (25mg/m2) at weekly intervals. The response to treatment was assessed using standard UICC criteria (partial or complete response, stasis or progression of disease). The serum concentrations of the acute phase proteins; C‐reactive protein (CRP), retinol binding protein (RBP), α1‐antitrypsin (α1‐AT), transferrin (TF) and albumin were measured. A response to therapy occurred in the tumours of seven (29%) of the 24 patients (two complete and five partial responses). All patients who demonstrated a response to treatment had a serum albumin level of > 37 g/l and a CRP level of · 10 mg/l. In contrast, of the 17 patients who did not respond to therapy, 12 (71%) had a serum albumin of less than 37 g/dl and a CRP of greater than 10 mg/l. Examination of the survival times of the 12 patients who had a pretreatment serum albumin level of less than 37 g/l revealed that all had died within 12 months of cessation of therapy. However, 58% of patients with pretreatment serum albumin levels of greater than 37 g/l survived for longer than 12 months. These results have shown that (i) patients who respond to rIL‐2‐based therapy and (ii) those patients who have prolonged survival times, can be identified by pretreatment measurement of serum levels of acute phase proteins.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>7531626</pmid><doi>10.1111/j.1365-2249.1995.tb05524.x</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | acute phase response Acute-Phase Proteins - analysis Biological and medical sciences Biomarkers, Tumor - blood Colorectal Neoplasms - blood Colorectal Neoplasms - mortality Colorectal Neoplasms - therapy Combined Modality Therapy Fluorouracil - therapeutic use Gastroenterology. Liver. Pancreas. Abdomen Humans IL‐2 therapy Interleukin-2 - therapeutic use Leucovorin - therapeutic use Medical sciences Neoplasm Metastasis Recombinant Proteins - therapeutic use response and survival Stomach. Duodenum. Small intestine. Colon. Rectum. Anus Survival Analysis Tumors |
title | Acute phase proteins and recombinant IL‐2 therapy: prediction of response and survival in patients with colorectal cancer |
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