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肉瘤的 I 期和 II 期临床试验:对药物发现和开发的启示。

Phase I and phase II clinical trials in sarcoma: Implications for drug discovery and development.

机构信息

Department of Radiology, University of Pennsylvania, Philadelphia, Pennsylvania.

Pennsylvania Hematology Oncology at Pennsylvania Hospital, Philadelphia, Pennsylvania.

出版信息

Cancer Med. 2019 Feb;8(2):585-592. doi: 10.1002/cam4.1958. Epub 2019 Jan 10.

Abstract

BACKGROUND

There has been limited progress in the development of novel therapeutics for the treatment of sarcomas. A review of phase I and II clinical trials for sarcomas may give insight into factors influencing sarcoma drug development.

METHODS

An exhaustive analysis of phase I and II clinical trials testing drugs for human sarcoma patients between 1 January 2000 and 1 June 2018 was performed using the PubMed search engine, the Thomson Web of Science, and the National Clinical Trials registry. Recorded outcomes included tested drugs, tested histological subtypes, whether the drug was initially developed for sarcoma, reported funding sources, and whether studies led to phase III trials.

RESULTS

Out of 238 studies meeting inclusion criteria, 87% (207 studies) reported funding sources. Of these, 59.9% (124/207) reported industry funding, 52.7% (109/207) reported government funding, and 27.5% (57/207) reported private funding. Only 5% (12/238) of phase I and II trials resulted in phase III trials, with 11 of 12 studies funded by industry. Approximately 90% (214/238) of studies tested drugs that were not initially tested in sarcoma, and 60.1% (143/238) of studies grouped different sarcoma histological subtypes together in the same study.

CONCLUSION

Industry has funded the majority of phase I and II sarcoma clinical trials that have led to phase III trials. There was a high rate of drugs approved for other cancers and then secondarily tested in sarcoma. Most trials tended to group different sarcoma subtypes rather than studying each subtype separately.

摘要

背景

新型治疗药物在肉瘤治疗方面的发展进展有限。对肉瘤的 I 期和 II 期临床试验进行回顾,可能有助于了解影响肉瘤药物开发的因素。

方法

使用 PubMed 搜索引擎、Thomson Web of Science 和国家临床试验注册处,对 2000 年 1 月 1 日至 2018 年 6 月 1 日期间用于人类肉瘤患者的 I 期和 II 期临床试验进行了全面分析。记录的结果包括测试药物、测试的组织学亚型、药物是否最初开发用于肉瘤、报告的资金来源以及研究是否导致 III 期试验。

结果

在符合纳入标准的 238 项研究中,87%(207 项)报告了资金来源。其中,59.9%(124/207)报告了工业资金,52.7%(109/207)报告了政府资金,27.5%(57/207)报告了私人资金。只有 5%(12/238)的 I 期和 II 期试验导致 III 期试验,其中 11 项研究由工业资助。大约 90%(214/238)的研究测试了最初未在肉瘤中测试的药物,60.1%(143/238)的研究将不同的肉瘤组织学亚型组合在同一研究中。

结论

工业界资助了大多数导致 III 期试验的 I 期和 II 期肉瘤临床试验。有很高比例的药物最初是为其他癌症批准的,然后在肉瘤中进行了二次测试。大多数试验倾向于将不同的肉瘤亚型分组,而不是分别研究每个亚型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20ac/6382713/5ee70b3cd6c9/CAM4-8-585-g001.jpg

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