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
Hauptverfasser: 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
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container_end_page e0204117
container_issue 9
container_start_page e0204117
container_title PloS one
container_volume 13
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
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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. 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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. 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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. 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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 system</topic><topic>Gastrointestinal tract</topic><topic>Gastrointestinal tumors</topic><topic>Hospitals</topic><topic>Humans</topic><topic>Imatinib</topic><topic>Imatinib mesylate</topic><topic>Imatinib Mesylate - administration &amp; dosage</topic><topic>Imatinib Mesylate - adverse effects</topic><topic>Inhibitor drugs</topic><topic>Life Sciences</topic><topic>Male</topic><topic>Medical diagnosis</topic><topic>Medical prognosis</topic><topic>Medical research</topic><topic>Medicine and Health Sciences</topic><topic>Mesenchyme</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>Middle Aged</topic><topic>Mutation</topic><topic>Neoplasm Metastasis</topic><topic>Neoplasms</topic><topic>Oncology</topic><topic>Pain</topic><topic>Patients</topic><topic>People and Places</topic><topic>Prognosis</topic><topic>Proto-Oncogene Proteins c-kit - genetics</topic><topic>Quality of life</topic><topic>Research and Analysis Methods</topic><topic>Risk factors</topic><topic>Studies</topic><topic>Survival</topic><topic>Targeted cancer therapy</topic><topic>Treatment Outcome</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Opposing Viewpoints in Context (Gale)</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Proquest Nursing &amp; 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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>
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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
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