Evaluation of drug lag and drug loss in Japan: participation in global phase III oncology trials.

IF 2.4 3区 医学 Q3 ONCOLOGY
Kaname Shiga, Taro Shibata, Toshio Miyata
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引用次数: 0

Abstract

Background: Despite efforts to mitigate drug lag, discrepancies in drug approval timelines persist between Japan and the US, and increase in unapproved drugs has become a significant challenge. This study aimed to evaluate potential drug lag and drug loss by assessing Japan's participation in global phase III multinational/multiregional clinical trials (MRCTs) targeted cancers.

Methods: Phase III MRCTs of anticancer drugs initiated between 2008 and 2022 were collected. Information of participant countries, study sponsor, study design, and cancer type were collected and analyzed by logistic regression analysis to identify factors affected Japan's participation.

Results: Of 999 phase III MRCTs, Japan's participation every 5 years increased over 15 years (2008-2012: 34.3%, 2013-2017: 51.6%, 2018-2022: 60.2%), while Japan's non-participation numbers did not change (2008-2012: 157, 2013-2017: 167, 2018-2022: 165). In the multivariate logistic regression analysis, the absence of an operational base in Japan and minor cancers were negatively associated with Japan's participation in phase III MRCTs. Japan's participation was also associated with some cancer organs and drug modalities.

Conclusion: Potential future drug lag and increases of unapproved drugs were expected to increase. Since the inclusion of Japan in MRCTs results in shorter or no approval lag, Japan should promote to make circumstances where small overseas companies can include Japan in MRCTs.

日本药物滞后性和药物损失的评估:参与全球III期肿瘤试验。
背景:尽管努力减轻药物滞后,但日本和美国在药物批准时间表上的差异仍然存在,未批准药物的增加已成为一个重大挑战。本研究旨在通过评估日本参与针对癌症的全球III期多国/多地区临床试验(mrct)来评估潜在的药物滞后和药物损失。方法:收集2008年至2022年间上市的抗癌药物的III期mrct。收集了参与国、研究发起者、研究设计和癌症类型的信息,并通过logistic回归分析来确定影响日本参与的因素。结果:在999例III期mrct中,日本每5年的参与人数在15年内增加(2008-2012年:34.3%,2013-2017年:51.6%,2018-2022年:60.2%),而日本未参与人数没有变化(2008-2012年:157人,2013-2017年:167人,2018-2022年:165人)。在多变量logistic回归分析中,日本缺乏运营基地和轻微癌症与日本参与III期mrct呈负相关。日本的参与还与某些癌症器官和药物方式有关。结论:未来潜在的药物滞后和未获批准药物的增加预计会增加。如果将日本纳入mrct,可以缩短或消除审批延迟,因此,日本应努力创造海外中小企业可以将日本纳入mrct的环境。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.80
自引率
3.00%
发文量
175
审稿时长
2 months
期刊介绍: The International Journal of Clinical Oncology (IJCO) welcomes original research papers on all aspects of clinical oncology that report the results of novel and timely investigations. Reports on clinical trials are encouraged. Experimental studies will also be accepted if they have obvious relevance to clinical oncology. Membership in the Japan Society of Clinical Oncology is not a prerequisite for submission to the journal. Papers are received on the understanding that: their contents have not been published in whole or in part elsewhere; that they are subject to peer review by at least two referees and the Editors, and to editorial revision of the language and contents; and that the Editors are responsible for their acceptance, rejection, and order of publication.
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