The landscape of investigator-initiated oncology trials conducted in mainland China during the past decade (2010–2019)

Cancer Innovation Pub Date : 2023-03-01 DOI:10.1002/cai2.58
Ye Cao, Lin-Miao Ye, Zhong Fan, Wei Yang, Li-Ying Chen, Yun Mei, De-Ying He, Wen-Jin Mo
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Abstract

The number of clinical trials conducted in mainland China, including investigator-initiated trials (IITs), has increased rapidly in recent years. However, there are few data on the characteristics of cancer-related IITs. We performed a comprehensive analysis of the landscape of cancer-related IITs in mainland China in the past decade. All cancer-related IITs registered on two clinical trial registries in the United States (www.clinicaltrials.gov, CT.gov) and mainland China (www.chictr.org.cn, ChiCTR) from 2010 to 2019 were identified. IITs were reviewed manually to validate classification, subcategorized by cancer type, and stratified by design characteristics to facilitate comparison across cancer types and with other specialties. A total of 8199 cancer-related IITs were identified. The number of trials registered annually increased over time, especially in the last 5 years. Although interventional studies were predominant, randomized double-blind studies accounted for only 8% of IITs. In the past decade, the trend for interventional studies conducted with different drugs increased year on year, although the increase in hormonal therapy IITs was not significant. Additionally, cancer-related IITs were unevenly geographically distributed, with half concentrated in the economically developed cities Shanghai, Beijing, and Guangdong. We also found an increase in registration before participant enrollment (64.9% for trials in conducted in 2015–2019 vs. 40.2% in 2010–2014, p < 0.001) and data monitoring committee use (44.5% vs. 40.0%, p = 0.001) and a decrease in randomization (51.5% vs. 62.7%, p < 0.001) and funding (36.4% vs. 56.3%, p < 0.001) between these periods. We also observed changes in intervention type (decrease in cytotoxic drug therapy [34.8% vs. 48.9%, p < 0.001]; increase in targeted therapy [17.8% vs. 14.2%, p = 0.004], immune checkpoint inhibitor therapy [6.6% vs. 0.0%, p < 0.001], and immune cell therapy [9.6% vs. 4.5%, p < 0.001]). Details of cancer-related IITs conducted during the past decade illustrate the merits of oncology research in mainland China. Although the increased quantity of IITs is encouraging, limitations remain regarding the quality of clinical trials, regional imbalances, and funding allocation.

Abstract Image

过去十年(2010-2019年)在中国大陆进行的研究者启动的肿瘤学试验的情况
近年来,在中国大陆进行的临床试验(包括研究者启动的试验)数量迅速增加。然而,关于癌症相关IIT的特征的数据很少。我们对过去十年中国大陆癌症相关IIT的情况进行了全面分析。确定了2010年至2019年在美国(www.clinicaltrials.gov,CT.gov)和中国大陆(www.chictr.org.cn,chictr)两个临床试验注册中心注册的所有癌症相关IIT。人工审查IIT以验证分类,按癌症类型进行子分类,并按设计特征进行分层,以促进癌症类型和其他专业的比较。共鉴定出8199个与癌症相关的IIT。随着时间的推移,每年登记的试验数量都在增加,尤其是在过去5年。尽管介入研究占主导地位,但随机双盲研究仅占IIT的8%。在过去的十年中,使用不同药物进行的介入研究的趋势逐年增加,尽管激素治疗IIT的增加并不显著。此外,与癌症相关的IIT在地理上分布不均,其中一半集中在经济发达的城市上海、北京和广东。我们还发现,参与者注册前的注册人数有所增加(2015-2019年进行的试验为64.9%,而2010-2014年为40.2%,p <; 0.001)和数据监测委员会使用(44.5%对40.0%,p = 0.001)和随机化减少(51.5%对62.7%,p <; 0.001)和资金(36.4%对56.3%,p <; 0.001)。我们还观察到干预类型的变化(细胞毒性药物治疗的减少[34.8%vs.48.9%,p <; 0.001];靶向治疗增加[17.8%vs.14.2%,p = 0.004],免疫检查点抑制剂治疗[6.6%vs.0.0%,p <; 0.001]和免疫细胞治疗[9.6%vs.4.5%,p <; 0.001])。过去十年中进行的癌症相关IIT的详细信息说明了中国大陆肿瘤学研究的优点。尽管IIT数量的增加令人鼓舞,但在临床试验的质量、区域失衡和资金分配方面仍然存在局限性。
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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