Suppr超能文献

日本罕见癌症治疗开发的现状及改善建议。

Current state of therapeutic development for rare cancers in Japan, and proposals for improvement.

机构信息

Subcommittee on Rare Cancers, The Science Board to the Pharmaceuticals and Medical Devices Agency, Tokyo, Japan.

Department of Musculoskeletal Oncology and Rehabilitation, Rare Cancer Center, National Cancer Center Hospital, Tokyo, Japan.

出版信息

Cancer Sci. 2018 May;109(5):1731-1737. doi: 10.1111/cas.13568.

Abstract

This article discusses current obstacles to the rapid development of safe and effective treatments for rare cancers, and considers measures required to overcome these challenges. In order to develop novel clinical options for rare cancers, which tend to remain left out of novel therapeutic development because of their paucity, efficient recruitment of eligible patients, who tend to be widely dispersed across the country and treated at different centers, is necessary. For this purpose, it is important to establish rare cancer registries that are linked with clinical studies, to organize a central pathological diagnosis system and biobanks for rare cancers, and to consolidate patients with rare cancers to facilities that can conduct clinical studies meeting international standards. Establishing an all-Japan cooperative network is essential. Clinical studies of rare cancers have considerable limitations in study design and sample size as a result of paucity of eligible patients and, as a result, the level of confirmation of the efficacy and safety shown by the studies is relatively low. Therefore, measures to alleviate these weaknesses inherent to external conditions need to be explored. It is also important to reform the current research environment in order to develop world-leading treatment for rare cancers, including promotion of basic research, collaboration between industry and academia, and improvement of the infrastructure for clinical studies. Collaboration among a wide range of stakeholders is required to promote the clinical development of treatment for rare cancers under a nationwide consensus.

摘要

本文讨论了当前阻碍安全有效治疗罕见癌症快速发展的障碍,并考虑了克服这些挑战所需的措施。为了为罕见癌症开发新的临床选择,由于其罕见性,往往被排除在新的治疗开发之外,需要有效地招募合格的患者,这些患者往往分布在全国各地,并在不同的中心接受治疗。为此,重要的是要建立与临床研究相关的罕见癌症登记处,组织中央病理诊断系统和罕见癌症生物库,并将罕见癌症患者集中到能够进行符合国际标准的临床研究的设施中。建立全日本合作网络至关重要。由于合格患者数量少,罕见癌症的临床研究在研究设计和样本量方面存在相当大的局限性,因此研究中显示的疗效和安全性的确认水平相对较低。因此,需要探索减轻这些固有外部条件弱点的措施。为了开发治疗罕见癌症的世界领先疗法,包括促进基础研究、工业界和学术界的合作以及改善临床研究基础设施,还需要改革当前的研究环境。需要广泛的利益相关者之间的合作,以在全国共识的基础上促进罕见癌症治疗的临床发展。

相似文献

2
The future of Cochrane Neonatal.考克兰新生儿协作网的未来。
Early Hum Dev. 2020 Nov;150:105191. doi: 10.1016/j.earlhumdev.2020.105191. Epub 2020 Sep 12.
6
Critical Care Network in the State of Qatar.卡塔尔国重症监护网络。
Qatar Med J. 2019 Nov 7;2019(2):2. doi: 10.5339/qmj.2019.qccc.2. eCollection 2019.
8
The burden of rare cancer in Japan: application of the RARECARE definition.日本罕见癌症的负担:RARECARE定义的应用
Cancer Epidemiol. 2014 Oct;38(5):490-5. doi: 10.1016/j.canep.2014.07.014. Epub 2014 Aug 22.

本文引用的文献

6
Driving gene-engineered T cell immunotherapy of cancer.驱动癌症的基因工程T细胞免疫疗法。
Cell Res. 2017 Jan;27(1):38-58. doi: 10.1038/cr.2016.154. Epub 2016 Dec 27.
7
Seamless Oncology-Drug Development.无缝肿瘤药物研发
N Engl J Med. 2016 May 26;374(21):2001-3. doi: 10.1056/NEJMp1603747. Epub 2016 Apr 13.
10
Neofunction of ACVR1 in fibrodysplasia ossificans progressiva.激活素受体1型在进行性骨化性纤维发育不良中的新功能
Proc Natl Acad Sci U S A. 2015 Dec 15;112(50):15438-43. doi: 10.1073/pnas.1510540112. Epub 2015 Nov 30.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验