EPIGIST: An observational real-life study on patients with metastatic gastrointestinal stromal tumors receiving imatinib
Gastrointestinal stromal tumors (GISTs) are rare, but represent the most common mesenchymal neoplasms of the gastrointestinal tract. EPIdemiology GIST, is an observational multicenter longitudinal follow-up cohort study reporting the prescribing patterns of imatinib in patients with GIST and the imp...
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Veröffentlicht in: | PloS one 2018-09, Vol.13 (9), p.e0204117-e0204117 |
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creator | Bouché, Olivier Cesne, Axel Le Rios, Maria Chaigneau, Loic Italiano, Antoine Duffaud, Florence Lecomte, Thierry Arsène, Dominique Manfredi, Sylvain Aparicio, Thomas Remy, Stéphane Isambert, Nicolas Collard, Olivier Priou, Frank Bertucci, François Sambuc, Roland Bisot-Locard, Ségolene Bourges, Olivier Chabaud, Sylvie Blay, Jean-Yves |
description | Gastrointestinal stromal tumors (GISTs) are rare, but represent the most common mesenchymal neoplasms of the gastrointestinal tract. EPIdemiology GIST, is an observational multicenter longitudinal follow-up cohort study reporting the prescribing patterns of imatinib in patients with GIST and the impact of the treatment in a real-world (standard clinical) setting.
Eligible patients had a confirmed diagnosis of unresectable or metastatic KIT-positive GIST and started treatment with imatinib for the first time between May 24, 2002, and June 30, 2010. During routine visits, annual collection of clinical characteristics was requested, i.e., age, GIST stage at diagnosis, history, imatinib treatment duration and dosage, adherence, and concomitant medications. Survival outcomes were estimated using the Kaplan-Meier method. Other data were analyzed using descriptive statistics.
Of 151 patients enrolled, imatinib was initiated for 126 patients before enrollment and for 25 patients on the day of enrollment or soon after. The patient characteristics were similar to those in published prospective trials. The estimated 1-, 2-, 3-, and 4-year overall survival rates were 90.4% (95% confidence interval [CI; 84.8%-94.0%]), 84.7% (95% CI [78.1%-89.4%]), 73.0% (95% CI [65.0%-79.4%]), and 60.7% (95% CI [51.4%-68.8%]), respectively. The most common adverse events (AEs) were diarrhea (39%), asthenia (39%), eyelid or periorbital edema (32%), abdominal pain (23%), and anemia (21%). Eight of 126 serious AEs were possibly related to the treatment as assessed by investigators.
Study results showed that patients in real-life populations are generally treated in accordance with national and international clinical recommendations and have outcomes comparable to those of patients in clinical trials. |
doi_str_mv | 10.1371/journal.pone.0204117 |
format | Article |
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Eligible patients had a confirmed diagnosis of unresectable or metastatic KIT-positive GIST and started treatment with imatinib for the first time between May 24, 2002, and June 30, 2010. During routine visits, annual collection of clinical characteristics was requested, i.e., age, GIST stage at diagnosis, history, imatinib treatment duration and dosage, adherence, and concomitant medications. Survival outcomes were estimated using the Kaplan-Meier method. Other data were analyzed using descriptive statistics.
Of 151 patients enrolled, imatinib was initiated for 126 patients before enrollment and for 25 patients on the day of enrollment or soon after. The patient characteristics were similar to those in published prospective trials. The estimated 1-, 2-, 3-, and 4-year overall survival rates were 90.4% (95% confidence interval [CI; 84.8%-94.0%]), 84.7% (95% CI [78.1%-89.4%]), 73.0% (95% CI [65.0%-79.4%]), and 60.7% (95% CI [51.4%-68.8%]), respectively. The most common adverse events (AEs) were diarrhea (39%), asthenia (39%), eyelid or periorbital edema (32%), abdominal pain (23%), and anemia (21%). Eight of 126 serious AEs were possibly related to the treatment as assessed by investigators.
Study results showed that patients in real-life populations are generally treated in accordance with national and international clinical recommendations and have outcomes comparable to those of patients in clinical trials.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0204117</identifier><identifier>PMID: 30226855</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Adult ; Aged ; Anemia ; Asthenia ; Cancer ; Cell proliferation ; Chemotherapy ; Clinical trials ; Confidence intervals ; Data processing ; Diagnosis ; Diarrhea ; Disease-Free Survival ; Dosage and administration ; Drug dosages ; Drug-Related Side Effects and Adverse Reactions - classification ; Drug-Related Side Effects and Adverse Reactions - diagnosis ; Drug-Related Side Effects and Adverse Reactions - pathology ; Edema ; Edema - chemically induced ; Edema - pathology ; Epidemiology ; Eyelid ; FDA approval ; Female ; Follow-Up Studies ; Gastroenterology ; Gastrointestinal cancer ; Gastrointestinal Stromal Tumors - complications ; Gastrointestinal Stromal Tumors - diagnosis ; Gastrointestinal Stromal Tumors - drug therapy ; Gastrointestinal Stromal Tumors - pathology ; Gastrointestinal system ; Gastrointestinal tract ; Gastrointestinal tumors ; Hospitals ; Humans ; Imatinib ; Imatinib mesylate ; Imatinib Mesylate - administration & dosage ; Imatinib Mesylate - adverse effects ; Inhibitor drugs ; Life Sciences ; Male ; Medical diagnosis ; Medical prognosis ; Medical research ; Medicine and Health Sciences ; Mesenchyme ; Metastases ; Metastasis ; Middle Aged ; Mutation ; Neoplasm Metastasis ; Neoplasms ; Oncology ; Pain ; Patients ; People and Places ; Prognosis ; Proto-Oncogene Proteins c-kit - genetics ; Quality of life ; Research and Analysis Methods ; Risk factors ; Studies ; Survival ; Targeted cancer therapy ; Treatment Outcome ; Tumors</subject><ispartof>PloS one, 2018-09, Vol.13 (9), p.e0204117-e0204117</ispartof><rights>COPYRIGHT 2018 Public Library of Science</rights><rights>2018 Bouché et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><rights>2018 Bouché et al 2018 Bouché et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c726t-bb10da732f9f14015428bdf14c3199976a3c4022785019ed23f95a78d3c7fe413</citedby><cites>FETCH-LOGICAL-c726t-bb10da732f9f14015428bdf14c3199976a3c4022785019ed23f95a78d3c7fe413</cites><orcidid>0000-0002-8284-3743 ; 0000-0002-8540-5351 ; 0000-0001-5093-0212 ; 0000-0002-0157-0959 ; 0000-0001-7190-120X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6143255/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6143255/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2096,2915,23845,27901,27902,53766,53768,79343,79344</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30226855$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://u-bourgogne.hal.science/hal-02005925$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Bouché, Olivier</creatorcontrib><creatorcontrib>Cesne, Axel Le</creatorcontrib><creatorcontrib>Rios, Maria</creatorcontrib><creatorcontrib>Chaigneau, Loic</creatorcontrib><creatorcontrib>Italiano, Antoine</creatorcontrib><creatorcontrib>Duffaud, Florence</creatorcontrib><creatorcontrib>Lecomte, Thierry</creatorcontrib><creatorcontrib>Arsène, Dominique</creatorcontrib><creatorcontrib>Manfredi, Sylvain</creatorcontrib><creatorcontrib>Aparicio, Thomas</creatorcontrib><creatorcontrib>Remy, Stéphane</creatorcontrib><creatorcontrib>Isambert, Nicolas</creatorcontrib><creatorcontrib>Collard, Olivier</creatorcontrib><creatorcontrib>Priou, Frank</creatorcontrib><creatorcontrib>Bertucci, François</creatorcontrib><creatorcontrib>Sambuc, Roland</creatorcontrib><creatorcontrib>Bisot-Locard, Ségolene</creatorcontrib><creatorcontrib>Bourges, Olivier</creatorcontrib><creatorcontrib>Chabaud, Sylvie</creatorcontrib><creatorcontrib>Blay, Jean-Yves</creatorcontrib><title>EPIGIST: An observational real-life study on patients with metastatic gastrointestinal stromal tumors receiving imatinib</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Gastrointestinal stromal tumors (GISTs) are rare, but represent the most common mesenchymal neoplasms of the gastrointestinal tract. EPIdemiology GIST, is an observational multicenter longitudinal follow-up cohort study reporting the prescribing patterns of imatinib in patients with GIST and the impact of the treatment in a real-world (standard clinical) setting.
Eligible patients had a confirmed diagnosis of unresectable or metastatic KIT-positive GIST and started treatment with imatinib for the first time between May 24, 2002, and June 30, 2010. During routine visits, annual collection of clinical characteristics was requested, i.e., age, GIST stage at diagnosis, history, imatinib treatment duration and dosage, adherence, and concomitant medications. Survival outcomes were estimated using the Kaplan-Meier method. Other data were analyzed using descriptive statistics.
Of 151 patients enrolled, imatinib was initiated for 126 patients before enrollment and for 25 patients on the day of enrollment or soon after. The patient characteristics were similar to those in published prospective trials. The estimated 1-, 2-, 3-, and 4-year overall survival rates were 90.4% (95% confidence interval [CI; 84.8%-94.0%]), 84.7% (95% CI [78.1%-89.4%]), 73.0% (95% CI [65.0%-79.4%]), and 60.7% (95% CI [51.4%-68.8%]), respectively. The most common adverse events (AEs) were diarrhea (39%), asthenia (39%), eyelid or periorbital edema (32%), abdominal pain (23%), and anemia (21%). Eight of 126 serious AEs were possibly related to the treatment as assessed by investigators.
Study results showed that patients in real-life populations are generally treated in accordance with national and international clinical recommendations and have outcomes comparable to those of patients in clinical trials.</description><subject>Adult</subject><subject>Aged</subject><subject>Anemia</subject><subject>Asthenia</subject><subject>Cancer</subject><subject>Cell proliferation</subject><subject>Chemotherapy</subject><subject>Clinical trials</subject><subject>Confidence intervals</subject><subject>Data processing</subject><subject>Diagnosis</subject><subject>Diarrhea</subject><subject>Disease-Free Survival</subject><subject>Dosage and administration</subject><subject>Drug dosages</subject><subject>Drug-Related Side Effects and Adverse Reactions - classification</subject><subject>Drug-Related Side Effects and Adverse Reactions - diagnosis</subject><subject>Drug-Related Side Effects and Adverse Reactions - pathology</subject><subject>Edema</subject><subject>Edema - chemically induced</subject><subject>Edema - pathology</subject><subject>Epidemiology</subject><subject>Eyelid</subject><subject>FDA approval</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Gastroenterology</subject><subject>Gastrointestinal cancer</subject><subject>Gastrointestinal Stromal Tumors - complications</subject><subject>Gastrointestinal Stromal Tumors - diagnosis</subject><subject>Gastrointestinal Stromal Tumors - drug therapy</subject><subject>Gastrointestinal Stromal Tumors - pathology</subject><subject>Gastrointestinal system</subject><subject>Gastrointestinal tract</subject><subject>Gastrointestinal tumors</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Imatinib</subject><subject>Imatinib mesylate</subject><subject>Imatinib Mesylate - administration & dosage</subject><subject>Imatinib Mesylate - adverse effects</subject><subject>Inhibitor drugs</subject><subject>Life Sciences</subject><subject>Male</subject><subject>Medical diagnosis</subject><subject>Medical prognosis</subject><subject>Medical research</subject><subject>Medicine and Health Sciences</subject><subject>Mesenchyme</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Middle Aged</subject><subject>Mutation</subject><subject>Neoplasm Metastasis</subject><subject>Neoplasms</subject><subject>Oncology</subject><subject>Pain</subject><subject>Patients</subject><subject>People and Places</subject><subject>Prognosis</subject><subject>Proto-Oncogene Proteins c-kit - genetics</subject><subject>Quality of life</subject><subject>Research and Analysis Methods</subject><subject>Risk factors</subject><subject>Studies</subject><subject>Survival</subject><subject>Targeted cancer therapy</subject><subject>Treatment 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An observational real-life study on patients with metastatic gastrointestinal stromal tumors receiving imatinib</title><author>Bouché, Olivier ; Cesne, Axel Le ; Rios, Maria ; Chaigneau, Loic ; Italiano, Antoine ; Duffaud, Florence ; Lecomte, Thierry ; Arsène, Dominique ; Manfredi, Sylvain ; Aparicio, Thomas ; Remy, Stéphane ; Isambert, Nicolas ; Collard, Olivier ; Priou, Frank ; Bertucci, François ; Sambuc, Roland ; Bisot-Locard, Ségolene ; Bourges, Olivier ; Chabaud, Sylvie ; Blay, Jean-Yves</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c726t-bb10da732f9f14015428bdf14c3199976a3c4022785019ed23f95a78d3c7fe413</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Anemia</topic><topic>Asthenia</topic><topic>Cancer</topic><topic>Cell proliferation</topic><topic>Chemotherapy</topic><topic>Clinical trials</topic><topic>Confidence intervals</topic><topic>Data processing</topic><topic>Diagnosis</topic><topic>Diarrhea</topic><topic>Disease-Free Survival</topic><topic>Dosage and administration</topic><topic>Drug dosages</topic><topic>Drug-Related Side Effects and Adverse Reactions - classification</topic><topic>Drug-Related Side Effects and Adverse Reactions - diagnosis</topic><topic>Drug-Related Side Effects and Adverse Reactions - pathology</topic><topic>Edema</topic><topic>Edema - chemically induced</topic><topic>Edema - pathology</topic><topic>Epidemiology</topic><topic>Eyelid</topic><topic>FDA approval</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Gastroenterology</topic><topic>Gastrointestinal cancer</topic><topic>Gastrointestinal Stromal Tumors - complications</topic><topic>Gastrointestinal Stromal Tumors - diagnosis</topic><topic>Gastrointestinal Stromal Tumors - drug therapy</topic><topic>Gastrointestinal Stromal Tumors - pathology</topic><topic>Gastrointestinal 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one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bouché, Olivier</au><au>Cesne, Axel Le</au><au>Rios, Maria</au><au>Chaigneau, Loic</au><au>Italiano, Antoine</au><au>Duffaud, Florence</au><au>Lecomte, Thierry</au><au>Arsène, Dominique</au><au>Manfredi, Sylvain</au><au>Aparicio, Thomas</au><au>Remy, Stéphane</au><au>Isambert, Nicolas</au><au>Collard, Olivier</au><au>Priou, Frank</au><au>Bertucci, François</au><au>Sambuc, Roland</au><au>Bisot-Locard, Ségolene</au><au>Bourges, Olivier</au><au>Chabaud, Sylvie</au><au>Blay, Jean-Yves</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>EPIGIST: An observational real-life study on patients with metastatic gastrointestinal stromal tumors receiving imatinib</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2018-09-18</date><risdate>2018</risdate><volume>13</volume><issue>9</issue><spage>e0204117</spage><epage>e0204117</epage><pages>e0204117-e0204117</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Gastrointestinal stromal tumors (GISTs) are rare, but represent the most common mesenchymal neoplasms of the gastrointestinal tract. EPIdemiology GIST, is an observational multicenter longitudinal follow-up cohort study reporting the prescribing patterns of imatinib in patients with GIST and the impact of the treatment in a real-world (standard clinical) setting.
Eligible patients had a confirmed diagnosis of unresectable or metastatic KIT-positive GIST and started treatment with imatinib for the first time between May 24, 2002, and June 30, 2010. During routine visits, annual collection of clinical characteristics was requested, i.e., age, GIST stage at diagnosis, history, imatinib treatment duration and dosage, adherence, and concomitant medications. Survival outcomes were estimated using the Kaplan-Meier method. Other data were analyzed using descriptive statistics.
Of 151 patients enrolled, imatinib was initiated for 126 patients before enrollment and for 25 patients on the day of enrollment or soon after. The patient characteristics were similar to those in published prospective trials. The estimated 1-, 2-, 3-, and 4-year overall survival rates were 90.4% (95% confidence interval [CI; 84.8%-94.0%]), 84.7% (95% CI [78.1%-89.4%]), 73.0% (95% CI [65.0%-79.4%]), and 60.7% (95% CI [51.4%-68.8%]), respectively. The most common adverse events (AEs) were diarrhea (39%), asthenia (39%), eyelid or periorbital edema (32%), abdominal pain (23%), and anemia (21%). Eight of 126 serious AEs were possibly related to the treatment as assessed by investigators.
Study results showed that patients in real-life populations are generally treated in accordance with national and international clinical recommendations and have outcomes comparable to those of patients in clinical trials.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>30226855</pmid><doi>10.1371/journal.pone.0204117</doi><tpages>e0204117</tpages><orcidid>https://orcid.org/0000-0002-8284-3743</orcidid><orcidid>https://orcid.org/0000-0002-8540-5351</orcidid><orcidid>https://orcid.org/0000-0001-5093-0212</orcidid><orcidid>https://orcid.org/0000-0002-0157-0959</orcidid><orcidid>https://orcid.org/0000-0001-7190-120X</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2018-09, Vol.13 (9), p.e0204117-e0204117 |
issn | 1932-6203 1932-6203 |
language | eng |
recordid | cdi_plos_journals_2108827651 |
source | Public Library of Science (PLoS) Journals Open Access; MEDLINE; DOAJ Directory of Open Access Journals; EZB-FREE-00999 freely available EZB journals; PubMed Central; Free Full-Text Journals in Chemistry |
subjects | Adult Aged Anemia Asthenia Cancer Cell proliferation Chemotherapy Clinical trials Confidence intervals Data processing Diagnosis Diarrhea Disease-Free Survival Dosage and administration Drug dosages Drug-Related Side Effects and Adverse Reactions - classification Drug-Related Side Effects and Adverse Reactions - diagnosis Drug-Related Side Effects and Adverse Reactions - pathology Edema Edema - chemically induced Edema - pathology Epidemiology Eyelid FDA approval Female Follow-Up Studies Gastroenterology Gastrointestinal cancer Gastrointestinal Stromal Tumors - complications Gastrointestinal Stromal Tumors - diagnosis Gastrointestinal Stromal Tumors - drug therapy Gastrointestinal Stromal Tumors - pathology Gastrointestinal system Gastrointestinal tract Gastrointestinal tumors Hospitals Humans Imatinib Imatinib mesylate Imatinib Mesylate - administration & dosage Imatinib Mesylate - adverse effects Inhibitor drugs Life Sciences Male Medical diagnosis Medical prognosis Medical research Medicine and Health Sciences Mesenchyme Metastases Metastasis Middle Aged Mutation Neoplasm Metastasis Neoplasms Oncology Pain Patients People and Places Prognosis Proto-Oncogene Proteins c-kit - genetics Quality of life Research and Analysis Methods Risk factors Studies Survival Targeted cancer therapy Treatment Outcome Tumors |
title | EPIGIST: An observational real-life study on patients with metastatic gastrointestinal stromal tumors receiving imatinib |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-01T15%3A54%3A33IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=EPIGIST:%20An%20observational%20real-life%20study%20on%20patients%20with%20metastatic%20gastrointestinal%20stromal%20tumors%20receiving%20imatinib&rft.jtitle=PloS%20one&rft.au=Bouch%C3%A9,%20Olivier&rft.date=2018-09-18&rft.volume=13&rft.issue=9&rft.spage=e0204117&rft.epage=e0204117&rft.pages=e0204117-e0204117&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0204117&rft_dat=%3Cgale_plos_%3EA560248621%3C/gale_plos_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2108827651&rft_id=info:pmid/30226855&rft_galeid=A560248621&rft_doaj_id=oai_doaj_org_article_f0c54153aec14505837646d461a95a53&rfr_iscdi=true |