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Tumor Volume as an Alternative Response Measurement for Imatinib Treated GIST Patients
BACKGROUND: Assessment of tumor size changes is crucial in clinical trials and patient care. We compared imatinib-induced volume changes of liver metastases (LM) from gastro-intestinal stromal tumors (GIST) to RECIST and Choi criteria and their association with overall survival (OS). METHODS: LM fro...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3487791/ https://www.ncbi.nlm.nih.gov/pubmed/23133631 http://dx.doi.org/10.1371/journal.pone.0048372 |
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author | Schiavon, Gaia Ruggiero, Alessandro Schöffski, Patrick van der Holt, Bronno Bekers, Dave J. Eechoute, Karel Vandecaveye, Vincent Krestin, Gabriel P. Verweij, Jaap Sleijfer, Stefan Mathijssen, Ron H. J. |
author_facet | Schiavon, Gaia Ruggiero, Alessandro Schöffski, Patrick van der Holt, Bronno Bekers, Dave J. Eechoute, Karel Vandecaveye, Vincent Krestin, Gabriel P. Verweij, Jaap Sleijfer, Stefan Mathijssen, Ron H. J. |
author_sort | Schiavon, Gaia |
collection | PubMed |
description | BACKGROUND: Assessment of tumor size changes is crucial in clinical trials and patient care. We compared imatinib-induced volume changes of liver metastases (LM) from gastro-intestinal stromal tumors (GIST) to RECIST and Choi criteria and their association with overall survival (OS). METHODS: LM from 84 GIST patients (training and validation set) were evaluated using manual and semi-automated Computed Tomography measurements at baseline, after 3, 6 and 12 months of imatinib. The ability of uni-dimensional (1D) and three-dimensional (3D) measurements to detect size changes (increase/decrease) ≥20% was evaluated. Volumetric response cut-offs were derived from minimally relevant changes (+20/−30%) by RECIST, considering lesions as spherical or ellipsoidal. RESULTS: 3D measurements detected size changes ≥20% more frequently than 1D at every time-point (P≤0.008). 3D and Choi criteria registered more responses than RECIST at 3 and 6 months for 3D-spheres (P≤0.03) and at all time-points for 3D-ellipsoids and Choi criteria (P<0.001). Progressive disease by 3D criteria seems to better correlate to OS at late time-points than other criteria. CONCLUSION: Volume criteria (especially ellipsoids) classify a higher number of patients as imatinib-responders than RECIST. Volume discriminates size changes better than diameter in GIST and constitutes a feasible and robust method to evaluate response and predict patient benefit. |
format | Online Article Text |
id | pubmed-3487791 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-34877912012-11-06 Tumor Volume as an Alternative Response Measurement for Imatinib Treated GIST Patients Schiavon, Gaia Ruggiero, Alessandro Schöffski, Patrick van der Holt, Bronno Bekers, Dave J. Eechoute, Karel Vandecaveye, Vincent Krestin, Gabriel P. Verweij, Jaap Sleijfer, Stefan Mathijssen, Ron H. J. PLoS One Research Article BACKGROUND: Assessment of tumor size changes is crucial in clinical trials and patient care. We compared imatinib-induced volume changes of liver metastases (LM) from gastro-intestinal stromal tumors (GIST) to RECIST and Choi criteria and their association with overall survival (OS). METHODS: LM from 84 GIST patients (training and validation set) were evaluated using manual and semi-automated Computed Tomography measurements at baseline, after 3, 6 and 12 months of imatinib. The ability of uni-dimensional (1D) and three-dimensional (3D) measurements to detect size changes (increase/decrease) ≥20% was evaluated. Volumetric response cut-offs were derived from minimally relevant changes (+20/−30%) by RECIST, considering lesions as spherical or ellipsoidal. RESULTS: 3D measurements detected size changes ≥20% more frequently than 1D at every time-point (P≤0.008). 3D and Choi criteria registered more responses than RECIST at 3 and 6 months for 3D-spheres (P≤0.03) and at all time-points for 3D-ellipsoids and Choi criteria (P<0.001). Progressive disease by 3D criteria seems to better correlate to OS at late time-points than other criteria. CONCLUSION: Volume criteria (especially ellipsoids) classify a higher number of patients as imatinib-responders than RECIST. Volume discriminates size changes better than diameter in GIST and constitutes a feasible and robust method to evaluate response and predict patient benefit. Public Library of Science 2012-11-02 /pmc/articles/PMC3487791/ /pubmed/23133631 http://dx.doi.org/10.1371/journal.pone.0048372 Text en © 2012 Schiavon et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Schiavon, Gaia Ruggiero, Alessandro Schöffski, Patrick van der Holt, Bronno Bekers, Dave J. Eechoute, Karel Vandecaveye, Vincent Krestin, Gabriel P. Verweij, Jaap Sleijfer, Stefan Mathijssen, Ron H. J. Tumor Volume as an Alternative Response Measurement for Imatinib Treated GIST Patients |
title | Tumor Volume as an Alternative Response Measurement for Imatinib Treated GIST Patients |
title_full | Tumor Volume as an Alternative Response Measurement for Imatinib Treated GIST Patients |
title_fullStr | Tumor Volume as an Alternative Response Measurement for Imatinib Treated GIST Patients |
title_full_unstemmed | Tumor Volume as an Alternative Response Measurement for Imatinib Treated GIST Patients |
title_short | Tumor Volume as an Alternative Response Measurement for Imatinib Treated GIST Patients |
title_sort | tumor volume as an alternative response measurement for imatinib treated gist patients |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3487791/ https://www.ncbi.nlm.nih.gov/pubmed/23133631 http://dx.doi.org/10.1371/journal.pone.0048372 |
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