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Transitional dynamics in oncology clinical trials: evaluating the impact of Clinical Trials Act on cooperative groups

作者
Kenichi Nakamura,Koji Takeda,Akiko Moriya Saito,Miho Kato,Shinya Sato,Satoshi Nakagawa,Yasuyuki Kawamoto,Eiji Oki,Isamu Okamoto,Hiroaki Okamoto,Hiroshi G. Katayama,Junki Mizusawa,Harumi Kaba,Taro Shibata,Haruhiko Fukuda
出处
期刊:Japanese Journal of Clinical Oncology [Oxford University Press]
卷期号:54 (7): 748-752 被引量:3
标识
DOI:10.1093/jjco/hyae034
摘要

OBJECTIVE: large-scale multicentre clinical trials conducted by cooperative groups have generated a lot of evidence to establish better standard treatments. The Clinical Trials Act was enforced on 1 April 2018, in Japan, and it has remarkably increased the operational burden on investigators, but its long-term impact on cancer cooperative groups is unknown. METHODS: a survey was conducted across the nine major cooperative groups that constitute the Japan Cancer Trials Network to assess the impact of Clinical Trials Act on the number of newly initiated trials from fiscal year (from 1 April to 31 March) 2017 to 2022 and that of ongoing trials on 1 April in each year from 2018 to 2023. RESULTS: the number of newly initiated trials dropped from 38 trials in fiscal year 2017 to 26 trials in fiscal year 2018, surged to 50 trials in fiscal year 2019, but then gradually decreased to 25 trials by fiscal year 2022. Specified clinical trials decreased from 32 trials in fiscal year 2019 to 12 trials in fiscal year 2022. The number of ongoing trials was 220 trials in 2018, peaked at 245 trials in 2020, but then gradually decreased to 219 trials by 2023. The number of specified clinical trials has been in consistent decline. By April 2023, of the 20 ongoing non-specified clinical trials, nine adhered to Clinical Trials Act and 11 followed the Ethical Guidelines for Medical and Health Research Involving Human Subjects. CONCLUSION: the number of multicentre clinical trials in oncology gradually decreased after the Clinical Trials Act's enforcement, which underscores the need for comprehensive amendment of the Clinical Trials Act to streamline the operational process.

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