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CLRM-18 SCREEN FAILURES IN PHASE III GLIOBLASTOMA CLINICAL TRIALS

Glioblastoma (GBM) remains the most common and lethal malignant primary brain tumor in adult patients, with median overall survival ranging from 7 to 22 months. National Comprehensive Cancer Network guidelines encourage participation in clinical trials for both newly diagnosed and recurrent GBM pati...

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Autor principal: Peters, Katherine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9354194/
http://dx.doi.org/10.1093/noajnl/vdac078.038
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author Peters, Katherine
author_facet Peters, Katherine
author_sort Peters, Katherine
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description Glioblastoma (GBM) remains the most common and lethal malignant primary brain tumor in adult patients, with median overall survival ranging from 7 to 22 months. National Comprehensive Cancer Network guidelines encourage participation in clinical trials for both newly diagnosed and recurrent GBM patients. Multiple phase II trials in GBM have yielded promising, positive results, but the translation to phase III results is lacking and has failed to make strides in improving outcomes. These phase III trials universally require many participants, and the expenditure of phase III clinical trials is quite significant, with the median being 21.4 million dollars. With a paucity of ground-breaking phase III clinical trials and the cost expenditure to perform them, understanding screen failures in GBM clinical trials along with an evaluation of causes of screen failures is warranted. Using both ClinicalTrials.gov and PubMed, phase III clinical trials in GBM patients published from 1994 to 2021 were queried. This search, initially in ClinicalTrials.gov, involved using the terms: “glioblastoma” and “GBM” with filters “phase III,” “interventional,” “completed,” “suspended,” and “terminated.” This search was cross-referenced with PubMed for published full articles in English peer-reviewed journals. Fifty-one studies were identified, and 21 out of 51 were appropriate for evaluation of screen failures, with 15 being for newly diagnosed GBM and six being for recurrent GBM. Nine out of 21 (42.9%) did not publish information on screen failures, and in the remaining 12 studies, proportions of screen failures ranged from 0-84.0% for newly diagnosed studies and 9.2-23.2% for recurrent studies, with a combined median percentage of 28.9%. In this analysis, over one-fourth of patients screen failed for GBM clinical trials. Thus, it is prudent to explore the causes of these screen failures, their implications on clinical trial design, and their impact on patient outcomes clinically, financially, and holistically.
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spelling pubmed-93541942022-08-09 CLRM-18 SCREEN FAILURES IN PHASE III GLIOBLASTOMA CLINICAL TRIALS Peters, Katherine Neurooncol Adv Supplement Abstracts Glioblastoma (GBM) remains the most common and lethal malignant primary brain tumor in adult patients, with median overall survival ranging from 7 to 22 months. National Comprehensive Cancer Network guidelines encourage participation in clinical trials for both newly diagnosed and recurrent GBM patients. Multiple phase II trials in GBM have yielded promising, positive results, but the translation to phase III results is lacking and has failed to make strides in improving outcomes. These phase III trials universally require many participants, and the expenditure of phase III clinical trials is quite significant, with the median being 21.4 million dollars. With a paucity of ground-breaking phase III clinical trials and the cost expenditure to perform them, understanding screen failures in GBM clinical trials along with an evaluation of causes of screen failures is warranted. Using both ClinicalTrials.gov and PubMed, phase III clinical trials in GBM patients published from 1994 to 2021 were queried. This search, initially in ClinicalTrials.gov, involved using the terms: “glioblastoma” and “GBM” with filters “phase III,” “interventional,” “completed,” “suspended,” and “terminated.” This search was cross-referenced with PubMed for published full articles in English peer-reviewed journals. Fifty-one studies were identified, and 21 out of 51 were appropriate for evaluation of screen failures, with 15 being for newly diagnosed GBM and six being for recurrent GBM. Nine out of 21 (42.9%) did not publish information on screen failures, and in the remaining 12 studies, proportions of screen failures ranged from 0-84.0% for newly diagnosed studies and 9.2-23.2% for recurrent studies, with a combined median percentage of 28.9%. In this analysis, over one-fourth of patients screen failed for GBM clinical trials. Thus, it is prudent to explore the causes of these screen failures, their implications on clinical trial design, and their impact on patient outcomes clinically, financially, and holistically. Oxford University Press 2022-08-05 /pmc/articles/PMC9354194/ http://dx.doi.org/10.1093/noajnl/vdac078.038 Text en © The Author(s) 2022. Published by Oxford University Press, the Society for Neuro-Oncology and the European Association of Neuro-Oncology. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Supplement Abstracts
Peters, Katherine
CLRM-18 SCREEN FAILURES IN PHASE III GLIOBLASTOMA CLINICAL TRIALS
title CLRM-18 SCREEN FAILURES IN PHASE III GLIOBLASTOMA CLINICAL TRIALS
title_full CLRM-18 SCREEN FAILURES IN PHASE III GLIOBLASTOMA CLINICAL TRIALS
title_fullStr CLRM-18 SCREEN FAILURES IN PHASE III GLIOBLASTOMA CLINICAL TRIALS
title_full_unstemmed CLRM-18 SCREEN FAILURES IN PHASE III GLIOBLASTOMA CLINICAL TRIALS
title_short CLRM-18 SCREEN FAILURES IN PHASE III GLIOBLASTOMA CLINICAL TRIALS
title_sort clrm-18 screen failures in phase iii glioblastoma clinical trials
topic Supplement Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9354194/
http://dx.doi.org/10.1093/noajnl/vdac078.038
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