Asparagine Synthetase Expression and Phase I Study With L-Asparaginase Encapsulated in Red Blood Cells in Patients With Pancreatic Adenocarcinoma
Asparaginase encapsulated in erythrocytes (ERY-ASP) is a potentially effective drug in patients with pancreatic adenocarcinoma (PAC) with null/low asparagine synthetase (ASNS) expression. Our aims were to assess ASNS expression in PAC from a large cohort and its prognostic and/or predictive value an...
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Veröffentlicht in: | Pancreas 2015-10, Vol.44 (7), p.1141-1147 |
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creator | Bachet, Jean-Baptiste Gay, Fabien Maréchal, Raphaël Galais, Marie-Pierre Adenis, Antoine MsC, David Salako Cros, Jerome Demetter, Pieter Svrcek, Magali Bardier-Dupas, Armelle Emile, Jean-François Hammel, Pascal Ebenezer, Christelle Berlier, Willy Godfrin, Yann André, Thierry |
description | Asparaginase encapsulated in erythrocytes (ERY-ASP) is a potentially effective drug in patients with pancreatic adenocarcinoma (PAC) with null/low asparagine synthetase (ASNS) expression. Our aims were to assess ASNS expression in PAC from a large cohort and its prognostic and/or predictive value and to conduct a phase I trial with ERY-ASP in patients with metastatic PAC.
Asparagine synthetase expression was evaluated using immunohistochemistry in resected PAC (471 patients) and in pairs of primary tumor and metastases (55 patients). Twelve patients were included in the phase I trial and received a single administration of ERY-ASP (25-150 IU/kg).
Null/low ASNS expression was found in 79.4% of the resected PAC with a high concordance between primary tumor and metastases. Asparagine synthetase expression was significantly correlated with sex and CXCR4 expression. In the phase I trial, ERY-ASP was well tolerated by patients with metastatic PAC. No patient had DLTs, and 6 patients had at least 1 ERY-ASP causally related adverse event out of the 12 adverse events reported.
Given the high rate of PAC with null/low ASNS expression and the good tolerability profile of ERY-ASP, ERY-ASP should be evaluated in further clinical studies in metastatic PAC. |
doi_str_mv | 10.1097/MPA.0000000000000394 |
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Asparagine synthetase expression was evaluated using immunohistochemistry in resected PAC (471 patients) and in pairs of primary tumor and metastases (55 patients). Twelve patients were included in the phase I trial and received a single administration of ERY-ASP (25-150 IU/kg).
Null/low ASNS expression was found in 79.4% of the resected PAC with a high concordance between primary tumor and metastases. Asparagine synthetase expression was significantly correlated with sex and CXCR4 expression. In the phase I trial, ERY-ASP was well tolerated by patients with metastatic PAC. No patient had DLTs, and 6 patients had at least 1 ERY-ASP causally related adverse event out of the 12 adverse events reported.
Given the high rate of PAC with null/low ASNS expression and the good tolerability profile of ERY-ASP, ERY-ASP should be evaluated in further clinical studies in metastatic PAC.</description><identifier>ISSN: 0885-3177</identifier><identifier>EISSN: 1536-4828</identifier><identifier>DOI: 10.1097/MPA.0000000000000394</identifier><identifier>PMID: 26355551</identifier><language>eng</language><publisher>United States</publisher><subject>Adenocarcinoma - drug therapy ; Adenocarcinoma - enzymology ; Administration, Intravenous ; Adult ; Aged ; Antineoplastic Agents - administration & dosage ; Antineoplastic Agents - pharmacokinetics ; Antineoplastic Agents - therapeutic use ; Asparaginase - adverse effects ; Asparaginase - biosynthesis ; Asparaginase - therapeutic use ; Chemical and Drug Induced Liver Injury - etiology ; Cohort Studies ; Drug Hypersensitivity - etiology ; Erythrocyte Transfusion - adverse effects ; Erythrocyte Transfusion - methods ; Erythrocytes - enzymology ; Female ; Humans ; Immunohistochemistry ; Kaplan-Meier Estimate ; Male ; Middle Aged ; Outcome Assessment, Health Care - methods ; Outcome Assessment, Health Care - statistics & numerical data ; Pancreatic Neoplasms ; Pancreatic Neoplasms - drug therapy ; Pancreatic Neoplasms - enzymology ; Prognosis ; Proportional Hazards Models</subject><ispartof>Pancreas, 2015-10, Vol.44 (7), p.1141-1147</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c307t-1de5266e16dda06bc8cba9b036f9df40c99b14a72d919df7831c6acd76c698c03</citedby><cites>FETCH-LOGICAL-c307t-1de5266e16dda06bc8cba9b036f9df40c99b14a72d919df7831c6acd76c698c03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26355551$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bachet, Jean-Baptiste</creatorcontrib><creatorcontrib>Gay, Fabien</creatorcontrib><creatorcontrib>Maréchal, Raphaël</creatorcontrib><creatorcontrib>Galais, Marie-Pierre</creatorcontrib><creatorcontrib>Adenis, Antoine</creatorcontrib><creatorcontrib>MsC, David Salako</creatorcontrib><creatorcontrib>Cros, Jerome</creatorcontrib><creatorcontrib>Demetter, Pieter</creatorcontrib><creatorcontrib>Svrcek, Magali</creatorcontrib><creatorcontrib>Bardier-Dupas, Armelle</creatorcontrib><creatorcontrib>Emile, Jean-François</creatorcontrib><creatorcontrib>Hammel, Pascal</creatorcontrib><creatorcontrib>Ebenezer, Christelle</creatorcontrib><creatorcontrib>Berlier, Willy</creatorcontrib><creatorcontrib>Godfrin, Yann</creatorcontrib><creatorcontrib>André, Thierry</creatorcontrib><title>Asparagine Synthetase Expression and Phase I Study With L-Asparaginase Encapsulated in Red Blood Cells in Patients With Pancreatic Adenocarcinoma</title><title>Pancreas</title><addtitle>Pancreas</addtitle><description>Asparaginase encapsulated in erythrocytes (ERY-ASP) is a potentially effective drug in patients with pancreatic adenocarcinoma (PAC) with null/low asparagine synthetase (ASNS) expression. Our aims were to assess ASNS expression in PAC from a large cohort and its prognostic and/or predictive value and to conduct a phase I trial with ERY-ASP in patients with metastatic PAC.
Asparagine synthetase expression was evaluated using immunohistochemistry in resected PAC (471 patients) and in pairs of primary tumor and metastases (55 patients). Twelve patients were included in the phase I trial and received a single administration of ERY-ASP (25-150 IU/kg).
Null/low ASNS expression was found in 79.4% of the resected PAC with a high concordance between primary tumor and metastases. Asparagine synthetase expression was significantly correlated with sex and CXCR4 expression. In the phase I trial, ERY-ASP was well tolerated by patients with metastatic PAC. No patient had DLTs, and 6 patients had at least 1 ERY-ASP causally related adverse event out of the 12 adverse events reported.
Given the high rate of PAC with null/low ASNS expression and the good tolerability profile of ERY-ASP, ERY-ASP should be evaluated in further clinical studies in metastatic PAC.</description><subject>Adenocarcinoma - drug therapy</subject><subject>Adenocarcinoma - enzymology</subject><subject>Administration, Intravenous</subject><subject>Adult</subject><subject>Aged</subject><subject>Antineoplastic Agents - administration & dosage</subject><subject>Antineoplastic Agents - pharmacokinetics</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Asparaginase - adverse effects</subject><subject>Asparaginase - biosynthesis</subject><subject>Asparaginase - therapeutic use</subject><subject>Chemical and Drug Induced Liver Injury - etiology</subject><subject>Cohort Studies</subject><subject>Drug Hypersensitivity - etiology</subject><subject>Erythrocyte Transfusion - adverse effects</subject><subject>Erythrocyte Transfusion - methods</subject><subject>Erythrocytes - enzymology</subject><subject>Female</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Kaplan-Meier Estimate</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Outcome Assessment, Health Care - methods</subject><subject>Outcome Assessment, Health Care - statistics & numerical data</subject><subject>Pancreatic Neoplasms</subject><subject>Pancreatic Neoplasms - drug therapy</subject><subject>Pancreatic Neoplasms - enzymology</subject><subject>Prognosis</subject><subject>Proportional Hazards Models</subject><issn>0885-3177</issn><issn>1536-4828</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkNFKwzAUhoMobk7fQCQv0Jk0bdJczjF1MLE4xctymqSu0qUlycA9hm9s53SI5-aHD75z8SF0ScmYEimuH_LJmPw9JpMjNKQp41GSxdkxGpIsSyNGhRigM-_fCaGCpfIUDWLO0v7oEH1OfAcO3mpr8HJrw8oE8AbPPjpnvK9bi8FqnK92cI6XYaO3-LUOK7yIDua3YBV0ftNAMBrXFj_1c9O0rcZT0zR-h3IItbHB7_0crHKmRwpPtLGtAqdq267hHJ1U0Hhz8bMj9HI7e57eR4vHu_l0sogUIyJEVJs05txQrjUQXqpMlSBLwngldZUQJWVJExCxlrQHImNUcVBacMVlpggboWT_V7nWe2eqonP1Gty2oKTYFS76wsX_wr12tde6Tbk2-iD9JmVfPY55GQ</recordid><startdate>201510</startdate><enddate>201510</enddate><creator>Bachet, Jean-Baptiste</creator><creator>Gay, Fabien</creator><creator>Maréchal, Raphaël</creator><creator>Galais, Marie-Pierre</creator><creator>Adenis, Antoine</creator><creator>MsC, David Salako</creator><creator>Cros, Jerome</creator><creator>Demetter, Pieter</creator><creator>Svrcek, Magali</creator><creator>Bardier-Dupas, Armelle</creator><creator>Emile, Jean-François</creator><creator>Hammel, Pascal</creator><creator>Ebenezer, Christelle</creator><creator>Berlier, Willy</creator><creator>Godfrin, Yann</creator><creator>André, Thierry</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>201510</creationdate><title>Asparagine Synthetase Expression and Phase I Study With L-Asparaginase Encapsulated in Red Blood Cells in Patients With Pancreatic Adenocarcinoma</title><author>Bachet, Jean-Baptiste ; Gay, Fabien ; Maréchal, Raphaël ; Galais, Marie-Pierre ; Adenis, Antoine ; MsC, David Salako ; Cros, Jerome ; Demetter, Pieter ; Svrcek, Magali ; Bardier-Dupas, Armelle ; Emile, Jean-François ; Hammel, Pascal ; Ebenezer, Christelle ; Berlier, Willy ; Godfrin, Yann ; André, Thierry</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c307t-1de5266e16dda06bc8cba9b036f9df40c99b14a72d919df7831c6acd76c698c03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adenocarcinoma - drug therapy</topic><topic>Adenocarcinoma - enzymology</topic><topic>Administration, Intravenous</topic><topic>Adult</topic><topic>Aged</topic><topic>Antineoplastic Agents - administration & dosage</topic><topic>Antineoplastic Agents - pharmacokinetics</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Asparaginase - adverse effects</topic><topic>Asparaginase - biosynthesis</topic><topic>Asparaginase - therapeutic use</topic><topic>Chemical and Drug Induced Liver Injury - etiology</topic><topic>Cohort Studies</topic><topic>Drug Hypersensitivity - etiology</topic><topic>Erythrocyte Transfusion - adverse effects</topic><topic>Erythrocyte Transfusion - methods</topic><topic>Erythrocytes - enzymology</topic><topic>Female</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Kaplan-Meier Estimate</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Outcome Assessment, Health Care - methods</topic><topic>Outcome Assessment, Health Care - statistics & numerical data</topic><topic>Pancreatic Neoplasms</topic><topic>Pancreatic Neoplasms - drug therapy</topic><topic>Pancreatic Neoplasms - enzymology</topic><topic>Prognosis</topic><topic>Proportional Hazards Models</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bachet, Jean-Baptiste</creatorcontrib><creatorcontrib>Gay, Fabien</creatorcontrib><creatorcontrib>Maréchal, Raphaël</creatorcontrib><creatorcontrib>Galais, Marie-Pierre</creatorcontrib><creatorcontrib>Adenis, Antoine</creatorcontrib><creatorcontrib>MsC, David Salako</creatorcontrib><creatorcontrib>Cros, Jerome</creatorcontrib><creatorcontrib>Demetter, Pieter</creatorcontrib><creatorcontrib>Svrcek, Magali</creatorcontrib><creatorcontrib>Bardier-Dupas, Armelle</creatorcontrib><creatorcontrib>Emile, Jean-François</creatorcontrib><creatorcontrib>Hammel, Pascal</creatorcontrib><creatorcontrib>Ebenezer, Christelle</creatorcontrib><creatorcontrib>Berlier, Willy</creatorcontrib><creatorcontrib>Godfrin, Yann</creatorcontrib><creatorcontrib>André, Thierry</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Pancreas</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bachet, Jean-Baptiste</au><au>Gay, Fabien</au><au>Maréchal, Raphaël</au><au>Galais, Marie-Pierre</au><au>Adenis, Antoine</au><au>MsC, David Salako</au><au>Cros, Jerome</au><au>Demetter, Pieter</au><au>Svrcek, Magali</au><au>Bardier-Dupas, Armelle</au><au>Emile, Jean-François</au><au>Hammel, Pascal</au><au>Ebenezer, Christelle</au><au>Berlier, Willy</au><au>Godfrin, Yann</au><au>André, Thierry</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Asparagine Synthetase Expression and Phase I Study With L-Asparaginase Encapsulated in Red Blood Cells in Patients With Pancreatic Adenocarcinoma</atitle><jtitle>Pancreas</jtitle><addtitle>Pancreas</addtitle><date>2015-10</date><risdate>2015</risdate><volume>44</volume><issue>7</issue><spage>1141</spage><epage>1147</epage><pages>1141-1147</pages><issn>0885-3177</issn><eissn>1536-4828</eissn><abstract>Asparaginase encapsulated in erythrocytes (ERY-ASP) is a potentially effective drug in patients with pancreatic adenocarcinoma (PAC) with null/low asparagine synthetase (ASNS) expression. Our aims were to assess ASNS expression in PAC from a large cohort and its prognostic and/or predictive value and to conduct a phase I trial with ERY-ASP in patients with metastatic PAC.
Asparagine synthetase expression was evaluated using immunohistochemistry in resected PAC (471 patients) and in pairs of primary tumor and metastases (55 patients). Twelve patients were included in the phase I trial and received a single administration of ERY-ASP (25-150 IU/kg).
Null/low ASNS expression was found in 79.4% of the resected PAC with a high concordance between primary tumor and metastases. Asparagine synthetase expression was significantly correlated with sex and CXCR4 expression. In the phase I trial, ERY-ASP was well tolerated by patients with metastatic PAC. No patient had DLTs, and 6 patients had at least 1 ERY-ASP causally related adverse event out of the 12 adverse events reported.
Given the high rate of PAC with null/low ASNS expression and the good tolerability profile of ERY-ASP, ERY-ASP should be evaluated in further clinical studies in metastatic PAC.</abstract><cop>United States</cop><pmid>26355551</pmid><doi>10.1097/MPA.0000000000000394</doi><tpages>7</tpages></addata></record> |
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subjects | Adenocarcinoma - drug therapy Adenocarcinoma - enzymology Administration, Intravenous Adult Aged Antineoplastic Agents - administration & dosage Antineoplastic Agents - pharmacokinetics Antineoplastic Agents - therapeutic use Asparaginase - adverse effects Asparaginase - biosynthesis Asparaginase - therapeutic use Chemical and Drug Induced Liver Injury - etiology Cohort Studies Drug Hypersensitivity - etiology Erythrocyte Transfusion - adverse effects Erythrocyte Transfusion - methods Erythrocytes - enzymology Female Humans Immunohistochemistry Kaplan-Meier Estimate Male Middle Aged Outcome Assessment, Health Care - methods Outcome Assessment, Health Care - statistics & numerical data Pancreatic Neoplasms Pancreatic Neoplasms - drug therapy Pancreatic Neoplasms - enzymology Prognosis Proportional Hazards Models |
title | Asparagine Synthetase Expression and Phase I Study With L-Asparaginase Encapsulated in Red Blood Cells in Patients With Pancreatic Adenocarcinoma |
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