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Prevalence of gastrointestinal stromal tumour (GIST) in the United Kingdom at different therapeutic lines: an epidemiologic model

BACKGROUND: The prevalence of patients with gastrointestinal stromal tumourgst (GIST) who fail currently available treatments imatinib and sunitinib (third-line treatment-eligible GIST) is unknown, but is expected to be below an ultra-orphan disease threshold of 2/100,000 population used in England...

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Autores principales: Starczewska Amelio, Justyna M, Cid Ruzafa, Javier, Desai, Kamal, Tzivelekis, Spiros, Muston, Dominic, Khalid, Javaria Mona, Ashman, Philip, Maguire, Andrew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4039646/
https://www.ncbi.nlm.nih.gov/pubmed/24884940
http://dx.doi.org/10.1186/1471-2407-14-364
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author Starczewska Amelio, Justyna M
Cid Ruzafa, Javier
Desai, Kamal
Tzivelekis, Spiros
Muston, Dominic
Khalid, Javaria Mona
Ashman, Philip
Maguire, Andrew
author_facet Starczewska Amelio, Justyna M
Cid Ruzafa, Javier
Desai, Kamal
Tzivelekis, Spiros
Muston, Dominic
Khalid, Javaria Mona
Ashman, Philip
Maguire, Andrew
author_sort Starczewska Amelio, Justyna M
collection PubMed
description BACKGROUND: The prevalence of patients with gastrointestinal stromal tumourgst (GIST) who fail currently available treatments imatinib and sunitinib (third-line treatment-eligible GIST) is unknown, but is expected to be below an ultra-orphan disease threshold of 2/100,000 population used in England and Wales. Our study was designed to estimate the prevalence and absolute number of UK patients with unresectable/metastatic GIST at first-, second- and eventually third-line treatment. METHODS: Our open population model estimates the probability that the prevalence of UK third-line treatment-eligible GIST patients will remain under the ultra-orphan disease threshold. Model parameters for incidence, proportion of unresectable/metastatic disease and survival estimates for GIST patients were obtained from a targeted literature review and a UK cancer register. The robustness of the results was checked through differing scenarios taking extreme values of the input parameters. RESULTS: The base-case scenario estimated a prevalence of third-line treatment-eligible GIST of 1/100,000 and a prevalence count of 598 with a 99.9% likelihood of being below the ultra-orphan disease threshold. The extreme scenarios, one-way and probabilistic sensitivity analyses and threshold analysis confirmed the robustness of these results. CONCLUSIONS: The prevalence of third-line treatment-eligible GIST is very low and highly likely below the ultra-orphan disease threshold.
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spelling pubmed-40396462014-06-01 Prevalence of gastrointestinal stromal tumour (GIST) in the United Kingdom at different therapeutic lines: an epidemiologic model Starczewska Amelio, Justyna M Cid Ruzafa, Javier Desai, Kamal Tzivelekis, Spiros Muston, Dominic Khalid, Javaria Mona Ashman, Philip Maguire, Andrew BMC Cancer Research Article BACKGROUND: The prevalence of patients with gastrointestinal stromal tumourgst (GIST) who fail currently available treatments imatinib and sunitinib (third-line treatment-eligible GIST) is unknown, but is expected to be below an ultra-orphan disease threshold of 2/100,000 population used in England and Wales. Our study was designed to estimate the prevalence and absolute number of UK patients with unresectable/metastatic GIST at first-, second- and eventually third-line treatment. METHODS: Our open population model estimates the probability that the prevalence of UK third-line treatment-eligible GIST patients will remain under the ultra-orphan disease threshold. Model parameters for incidence, proportion of unresectable/metastatic disease and survival estimates for GIST patients were obtained from a targeted literature review and a UK cancer register. The robustness of the results was checked through differing scenarios taking extreme values of the input parameters. RESULTS: The base-case scenario estimated a prevalence of third-line treatment-eligible GIST of 1/100,000 and a prevalence count of 598 with a 99.9% likelihood of being below the ultra-orphan disease threshold. The extreme scenarios, one-way and probabilistic sensitivity analyses and threshold analysis confirmed the robustness of these results. CONCLUSIONS: The prevalence of third-line treatment-eligible GIST is very low and highly likely below the ultra-orphan disease threshold. BioMed Central 2014-05-24 /pmc/articles/PMC4039646/ /pubmed/24884940 http://dx.doi.org/10.1186/1471-2407-14-364 Text en Copyright © 2014 Starczewska Amelio et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
spellingShingle Research Article
Starczewska Amelio, Justyna M
Cid Ruzafa, Javier
Desai, Kamal
Tzivelekis, Spiros
Muston, Dominic
Khalid, Javaria Mona
Ashman, Philip
Maguire, Andrew
Prevalence of gastrointestinal stromal tumour (GIST) in the United Kingdom at different therapeutic lines: an epidemiologic model
title Prevalence of gastrointestinal stromal tumour (GIST) in the United Kingdom at different therapeutic lines: an epidemiologic model
title_full Prevalence of gastrointestinal stromal tumour (GIST) in the United Kingdom at different therapeutic lines: an epidemiologic model
title_fullStr Prevalence of gastrointestinal stromal tumour (GIST) in the United Kingdom at different therapeutic lines: an epidemiologic model
title_full_unstemmed Prevalence of gastrointestinal stromal tumour (GIST) in the United Kingdom at different therapeutic lines: an epidemiologic model
title_short Prevalence of gastrointestinal stromal tumour (GIST) in the United Kingdom at different therapeutic lines: an epidemiologic model
title_sort prevalence of gastrointestinal stromal tumour (gist) in the united kingdom at different therapeutic lines: an epidemiologic model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4039646/
https://www.ncbi.nlm.nih.gov/pubmed/24884940
http://dx.doi.org/10.1186/1471-2407-14-364
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