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[2020年中国抗癌药物临床试验进展]

[Progress on clinical trials of cancer drugs in China, 2020].

作者信息

Wu D W, Huang H Y, Tang Y, Wang H X, Wang J, Wang S H, Fang H, Yang X Y, Li J, Wang X, Liu L J, Yan Y, Wang Q, Li N, Cao C, Xu B H, Sun Y, He J

机构信息

Department of Clinical Trials Center, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.

National Center for Drug Evaluation, National Medical Products Administration, Beijing 100022, China.

出版信息

Zhonghua Zhong Liu Za Zhi. 2021 Feb 23;43(2):218-223. doi: 10.3760/cma.j.cn112152-20201221-01089.

Abstract

To explore the latest progress of oncology drug clinical trials in China under COVID-19, as well as to provide decision-making evidence for related stakeholders. Research progress of oncology drug trials and approved cancer drugs in China in 2020 were systematically summarized and compared with 2019. Information Disclosure Platform for Drug Clinical Studies and China Food and Drug Administration Query System for Domestic and Imported Drug were searched for registered clinical trials and approved oncology drugs, respectively. The trial scope, stage, drug type, effect and mechanism of domestic and global pharmaceutical enterprises were compared between 2019 and 2020. A total of 722 cancer drug trials registered in China in 2020, with an annual growth rate of 52.3%, accounting for 28.3% of all registered trials. Among them, 603 (83.5%) trials were initiated by domestic pharmaceutical enterprises, and 105 (14.5%) were international multicenter trials, phase I trials accounted for 44.5%. For all those trials, there were 458 cancer drug varieties, with an annual growth rate of 36.7%, and 361 (85.8%) were developed by domestic enterprises. Most of the investigational products were therapeutic innovative drugs (77.1%), major in tumor treatment (92.8%). In terms of mechanism, targeted drugs were the most popular, accounting for 76.6%, and programmed cell death-1 (PD-1) and epithelial growth factor receptor (EGFR) were the most common targets. In addition, there were 19 anticancer drugs from 17 companies approved in China in 2019, with 10 drugs from domestic companies. Lung cancer and breast cancer are the most common indications for both registered trials and marketed drugs. No statistically significant differences were found between 2020 and 2019 in terms of the distribution of trial sponsor, scope and stage, as well as the distribution of drug type, effect and mechanism (>0.05). During the Covid-19 epidemic period, clinical trials of oncology drugs in China progress smoothly and maintain a high growth rate. Series of innovative products obtained by domestic enterprises in 2020 is the main driving force of development of oncology drug clinical trials in China.

摘要

为探究新型冠状病毒肺炎疫情下中国肿瘤药物临床试验的最新进展,并为相关利益者提供决策依据。系统总结2020年中国肿瘤药物试验及获批癌症药物的研究进展,并与2019年进行比较。分别在药物临床试验信息公示平台及国家药品监督管理局国产及进口药品查询系统中检索注册的临床试验及获批的肿瘤药物。比较2019年和2020年国内外制药企业的试验范围、阶段、药物类型、疗效及作用机制。2020年中国共登记722项癌症药物试验,年增长率为52.3%,占所有登记试验的28.3%。其中,603项(83.5%)试验由国内制药企业发起,105项(14.5%)为国际多中心试验,I期试验占44.5%。在所有这些试验中,有458个癌症药物品种,年增长率为36.7%,其中361个(85.8%)由国内企业研发。大多数研究产品为治疗性创新药物(77.1%),主要用于肿瘤治疗(92.8%)。在作用机制方面,靶向药物最受欢迎,占76.6%,程序性细胞死亡蛋白1(PD-1)和表皮生长因子受体(EGFR)是最常见的靶点。此外,2019年有17家公司的19种抗癌药物在中国获批,其中10种来自国内公司。肺癌和乳腺癌是登记试验和上市药物最常见的适应症。2020年与2019年相比,试验申办方、范围和阶段的分布以及药物类型、疗效和作用机制的分布均无统计学显著差异(>0.05)。在新型冠状病毒肺炎疫情期间,中国肿瘤药物临床试验进展顺利并保持较高增长率。国内企业在2020年获得的一系列创新产品是中国肿瘤药物临床试验发展的主要驱动力。

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