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The role of clinical trials in the sustainability of the Italian national health service cancer drug expenditure

OBJECTIVE: Clinical trials offer new and potentially more effective therapeutic options for cancer patients and a potential cost-saving opportunity, especially considering that trial drugs are provided free-of-charge. The aim of this study was to analyse drug-related cost savings in clinical trials...

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Autores principales: Gasperoni, Lorenzo, Cafaro, Alessandro, Ferretti, Eleonora, Di Iorio, Valentina, Nanni, Oriana, Masini, Carla
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9986930/
https://www.ncbi.nlm.nih.gov/pubmed/35577545
http://dx.doi.org/10.1136/ejhpharm-2022-003297
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author Gasperoni, Lorenzo
Cafaro, Alessandro
Ferretti, Eleonora
Di Iorio, Valentina
Nanni, Oriana
Masini, Carla
author_facet Gasperoni, Lorenzo
Cafaro, Alessandro
Ferretti, Eleonora
Di Iorio, Valentina
Nanni, Oriana
Masini, Carla
author_sort Gasperoni, Lorenzo
collection PubMed
description OBJECTIVE: Clinical trials offer new and potentially more effective therapeutic options for cancer patients and a potential cost-saving opportunity, especially considering that trial drugs are provided free-of-charge. The aim of this study was to analyse drug-related cost savings in clinical trials in a cancer institute over a 3 year period. The cost savings relate to the pharmaceutical expenditure of our centre, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) “Dino Amadori”. METHODS: We conducted a retrospective analysis of patients taking part in interventional clinical cancer trials approved by a local independent Ethics Committee between 1 January 2018 and 31 December 2020. The standard of care (SOC) was identified as the standard treatment that would have been offered to a patient if he/she had not been enrolled in the study. The sum of SOC costs of all patients represents the potential cost avoidance during the study period. Results were stratified by year, trial promoter, trial phase and tumour type. The same approach was used to perform a secondary analysis of compassionate use programmes. RESULT: In the 3 year analysis, 1,257 patients were treated with experimental therapies in 244 clinical trials, of which 157 were profit and 87 academic. Results showed an overall cost savings of €13,266,518, more than 50% of which (€7,035,009) was related to phase III studies. Profit clinical trials generated €9,069,764 (68.4%) of the drug cost savings compared with €4,196,754 (31.6%) of academic studies. The stratification for tumour type was €3,552,592 (26.8%) genitourinary cancer, €3,268,074 (24.6%) melanoma, €2,574,127 (19.4%) haematological malignancies, €2,330,791 (17.6%) lung cancer, €728,149 (5.5%) gastrointestinal cancer, €557,608 (4.2%) rare tumours and €255,178 (1.9%) breast cancer. The secondary analysis on compassionate use included 122 patients involved in 28 different access programmes and revealed cost savings of €1,649,550. CONCLUSION: The results of our analysis point to the benefits of participating in and planning clinical trials for the public healthcare sector.
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spelling pubmed-99869302023-03-07 The role of clinical trials in the sustainability of the Italian national health service cancer drug expenditure Gasperoni, Lorenzo Cafaro, Alessandro Ferretti, Eleonora Di Iorio, Valentina Nanni, Oriana Masini, Carla Eur J Hosp Pharm Original Research OBJECTIVE: Clinical trials offer new and potentially more effective therapeutic options for cancer patients and a potential cost-saving opportunity, especially considering that trial drugs are provided free-of-charge. The aim of this study was to analyse drug-related cost savings in clinical trials in a cancer institute over a 3 year period. The cost savings relate to the pharmaceutical expenditure of our centre, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) “Dino Amadori”. METHODS: We conducted a retrospective analysis of patients taking part in interventional clinical cancer trials approved by a local independent Ethics Committee between 1 January 2018 and 31 December 2020. The standard of care (SOC) was identified as the standard treatment that would have been offered to a patient if he/she had not been enrolled in the study. The sum of SOC costs of all patients represents the potential cost avoidance during the study period. Results were stratified by year, trial promoter, trial phase and tumour type. The same approach was used to perform a secondary analysis of compassionate use programmes. RESULT: In the 3 year analysis, 1,257 patients were treated with experimental therapies in 244 clinical trials, of which 157 were profit and 87 academic. Results showed an overall cost savings of €13,266,518, more than 50% of which (€7,035,009) was related to phase III studies. Profit clinical trials generated €9,069,764 (68.4%) of the drug cost savings compared with €4,196,754 (31.6%) of academic studies. The stratification for tumour type was €3,552,592 (26.8%) genitourinary cancer, €3,268,074 (24.6%) melanoma, €2,574,127 (19.4%) haematological malignancies, €2,330,791 (17.6%) lung cancer, €728,149 (5.5%) gastrointestinal cancer, €557,608 (4.2%) rare tumours and €255,178 (1.9%) breast cancer. The secondary analysis on compassionate use included 122 patients involved in 28 different access programmes and revealed cost savings of €1,649,550. CONCLUSION: The results of our analysis point to the benefits of participating in and planning clinical trials for the public healthcare sector. BMJ Publishing Group 2023-03 2022-05-16 /pmc/articles/PMC9986930/ /pubmed/35577545 http://dx.doi.org/10.1136/ejhpharm-2022-003297 Text en © European Association of Hospital Pharmacists 2023. Re-use permitted under CC BY-NC. No commercial re-use. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, an indication of whether changes were made, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Original Research
Gasperoni, Lorenzo
Cafaro, Alessandro
Ferretti, Eleonora
Di Iorio, Valentina
Nanni, Oriana
Masini, Carla
The role of clinical trials in the sustainability of the Italian national health service cancer drug expenditure
title The role of clinical trials in the sustainability of the Italian national health service cancer drug expenditure
title_full The role of clinical trials in the sustainability of the Italian national health service cancer drug expenditure
title_fullStr The role of clinical trials in the sustainability of the Italian national health service cancer drug expenditure
title_full_unstemmed The role of clinical trials in the sustainability of the Italian national health service cancer drug expenditure
title_short The role of clinical trials in the sustainability of the Italian national health service cancer drug expenditure
title_sort role of clinical trials in the sustainability of the italian national health service cancer drug expenditure
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9986930/
https://www.ncbi.nlm.nih.gov/pubmed/35577545
http://dx.doi.org/10.1136/ejhpharm-2022-003297
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