Addressing the drug development challenge for rare pediatric diseases in Japan: a case study of isotretinoin.

IF 2.7 3区 医学 Q2 ONCOLOGY
Shota Inoue, Akihiko Ozaki, Hayase Hakariya, Jungang Zhao, Ivan D Florez, Yoshihiko Morikawa, Tetsuya Tanimoto
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Abstract

Drug lag in rare pediatric diseases remains a significant challenge in Japan despite its sophisticated healthcare system. We examined this issue through a case study of isotretinoin, an established standard drug for high-risk neuroblastoma (affecting 45-60 new patients annually in Japan) since the 2000s that has not been granted regulatory approval in Japan as of 2025. Analysis of regulatory documents and clinical practices revealed that while isotretinoin has demonstrated improved event-free survival rates in international trials when used as maintenance therapy for high-risk neuroblastoma, multiple barriers have hindered its domestic approval. These include the challenges of conducting clinical trials in limited pediatric populations, substantial development costs, diminishing market attractiveness due to Japan's demographic shift, and restrictions on "mixed billing system" which means combining covered insurance treatments with uncovered treatments under the universal health insurance system in Japan. Currently, patients must rely on costly private imports or clinical trial participation to access the drug, leading to financial burdens and treatment discontinuation risks. Recent regulatory reforms, including the establishment of the Evaluation Committee on Unapproved or Off-labeled Drugs with High Medical Needs in 2009 and amendments enabling investigator-led trials, have facilitated progress. An investigator-led Phase II clinical trial evaluating isotretinoin's safety and efficacy is ongoing since 2023, with expected completion in 2026. However, the lengthy timeline of approximately 25 years from global adoption to potential approval highlights persistent challenges in pediatric drug development and Japan's isolation from global drug development networks. This case demonstrates the need for innovative policy approaches to ensure sustainable drug development for rare pediatric diseases in an aging society.

应对日本罕见儿科疾病的药物开发挑战:异维甲酸的案例研究。
尽管日本拥有先进的医疗体系,但罕见儿科疾病的药物滞后仍然是一个重大挑战。我们通过异维甲酸的案例研究来研究这一问题,异维甲酸是自2000年以来高风险神经母细胞瘤(日本每年影响45-60名新患者)的既定标准药物,截至2025年尚未获得日本监管机构的批准。对监管文件和临床实践的分析显示,虽然异维a酸在国际试验中被证明可以提高高风险神经母细胞瘤的无事件生存率,但多重障碍阻碍了其在国内的批准。这些挑战包括在有限的儿科人群中进行临床试验的挑战、巨大的开发成本、由于日本人口结构变化而导致的市场吸引力下降,以及对“混合计费系统”的限制,“混合计费系统”意味着在日本全民健康保险制度下将有保险治疗与无保险治疗相结合。目前,患者必须依靠昂贵的私人进口或临床试验参与来获得药物,从而导致经济负担和治疗中断风险。最近的监管改革,包括2009年成立了“高医疗需求的未经批准或标签外药品评估委员会”,以及允许研究者主导试验的修正案,都促进了进展。一项由研究者主导的评估异维甲酸安全性和有效性的II期临床试验自2023年开始进行,预计将于2026年完成。然而,从全球采用到潜在批准大约需要25年的漫长时间,这凸显了儿科药物开发面临的持续挑战,以及日本与全球药物开发网络的隔离。这一案例表明,在老龄化社会中,需要创新的政策方法来确保罕见儿科疾病的可持续药物开发。
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
7.60
自引率
0.00%
发文量
121
审稿时长
1 months
期刊介绍: The development of new anticancer agents is one of the most rapidly changing aspects of cancer research. Investigational New Drugs provides a forum for the rapid dissemination of information on new anticancer agents. The papers published are of interest to the medical chemist, toxicologist, pharmacist, pharmacologist, biostatistician and clinical oncologist. Investigational New Drugs provides the fastest possible publication of new discoveries and results for the whole community of scientists developing anticancer agents.
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