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Value assessment of NMPA-approved new cancer drugs for solid cancer in China, 2016–2020

BACKGROUND: Whether the high cost of cancer drugs is commensurate with their value to patients, which has become the focus of public concern. We aimed to assess the value of new cancer drugs approved for solid cancer in China and to explore the association between price and value of drugs. METHODS:...

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Autores principales: Luo, Jing, Ou, Shunlong, Wei, Hua, Qin, Xiaoli, Peng, Rui, Wang, Song, Jiang, Qian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9998930/
https://www.ncbi.nlm.nih.gov/pubmed/36908440
http://dx.doi.org/10.3389/fpubh.2023.1109668
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author Luo, Jing
Ou, Shunlong
Wei, Hua
Qin, Xiaoli
Peng, Rui
Wang, Song
Jiang, Qian
author_facet Luo, Jing
Ou, Shunlong
Wei, Hua
Qin, Xiaoli
Peng, Rui
Wang, Song
Jiang, Qian
author_sort Luo, Jing
collection PubMed
description BACKGROUND: Whether the high cost of cancer drugs is commensurate with their value to patients, which has become the focus of public concern. We aimed to assess the value of new cancer drugs approved for solid cancer in China and to explore the association between price and value of drugs. METHODS: We identified all new drugs for solid tumor that approved by the China's National Medical Products Administration (NMPA) between 2016 and 2020. The value of these drugs was assessed according to the American Society of Clinical Oncology Value Framework (ASCO-VF) and the European Society for Medical Oncology Magnitude of Clinical Benefit Scale (ESMO-MCBS). We calculated Cohen's κ statistic to describe agreement between the two frameworks. Spearman's correlation coefficient was used to evaluate the correlation between price and value of drugs. RESULTS: Between 2016 and 2020, 37 new drugs were approved by the NMPA for solid tumor and we could evaluate the value of 28 drugs (76%). Eight (29%) of drugs were approved for non-small-cell lung cancer and 6 (21%) for breast cancer. ASCO-VF scores had a range of −20 to 110.1, and the median score was 43.3 (inter-quartile range 27.1–58.35). Only seven drugs (25%) met the ASCO-VF cutoff score. By the ESMO-MCBS, 13 drugs showed a meaningful value. Agreement between these two frameworks thresholds was only fair (κ = 0.515, P < 0.05). We found no statistically significant correlation between launch price of drugs and clinical benefit according to both frameworks. CONCLUSIONS: Not all NMPA-approved new cancer drugs had meaningful value as measured by ASCO-VF or ESMO-MCBS. There was no significant correlation between drug price and the level of clinical benefit.
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spelling pubmed-99989302023-03-11 Value assessment of NMPA-approved new cancer drugs for solid cancer in China, 2016–2020 Luo, Jing Ou, Shunlong Wei, Hua Qin, Xiaoli Peng, Rui Wang, Song Jiang, Qian Front Public Health Public Health BACKGROUND: Whether the high cost of cancer drugs is commensurate with their value to patients, which has become the focus of public concern. We aimed to assess the value of new cancer drugs approved for solid cancer in China and to explore the association between price and value of drugs. METHODS: We identified all new drugs for solid tumor that approved by the China's National Medical Products Administration (NMPA) between 2016 and 2020. The value of these drugs was assessed according to the American Society of Clinical Oncology Value Framework (ASCO-VF) and the European Society for Medical Oncology Magnitude of Clinical Benefit Scale (ESMO-MCBS). We calculated Cohen's κ statistic to describe agreement between the two frameworks. Spearman's correlation coefficient was used to evaluate the correlation between price and value of drugs. RESULTS: Between 2016 and 2020, 37 new drugs were approved by the NMPA for solid tumor and we could evaluate the value of 28 drugs (76%). Eight (29%) of drugs were approved for non-small-cell lung cancer and 6 (21%) for breast cancer. ASCO-VF scores had a range of −20 to 110.1, and the median score was 43.3 (inter-quartile range 27.1–58.35). Only seven drugs (25%) met the ASCO-VF cutoff score. By the ESMO-MCBS, 13 drugs showed a meaningful value. Agreement between these two frameworks thresholds was only fair (κ = 0.515, P < 0.05). We found no statistically significant correlation between launch price of drugs and clinical benefit according to both frameworks. CONCLUSIONS: Not all NMPA-approved new cancer drugs had meaningful value as measured by ASCO-VF or ESMO-MCBS. There was no significant correlation between drug price and the level of clinical benefit. Frontiers Media S.A. 2023-02-24 /pmc/articles/PMC9998930/ /pubmed/36908440 http://dx.doi.org/10.3389/fpubh.2023.1109668 Text en Copyright © 2023 Luo, Ou, Wei, Qin, Peng, Wang and Jiang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Public Health
Luo, Jing
Ou, Shunlong
Wei, Hua
Qin, Xiaoli
Peng, Rui
Wang, Song
Jiang, Qian
Value assessment of NMPA-approved new cancer drugs for solid cancer in China, 2016–2020
title Value assessment of NMPA-approved new cancer drugs for solid cancer in China, 2016–2020
title_full Value assessment of NMPA-approved new cancer drugs for solid cancer in China, 2016–2020
title_fullStr Value assessment of NMPA-approved new cancer drugs for solid cancer in China, 2016–2020
title_full_unstemmed Value assessment of NMPA-approved new cancer drugs for solid cancer in China, 2016–2020
title_short Value assessment of NMPA-approved new cancer drugs for solid cancer in China, 2016–2020
title_sort value assessment of nmpa-approved new cancer drugs for solid cancer in china, 2016–2020
topic Public Health
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9998930/
https://www.ncbi.nlm.nih.gov/pubmed/36908440
http://dx.doi.org/10.3389/fpubh.2023.1109668
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