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葡萄膜黑色素瘤临床试验设计的特征:系统综述以确立难以捉摸的标准治疗。

Characterization of uveal melanoma clinical trial design: a systematic review to establish an elusive standard of care.

机构信息

Department of Biological Sciences, Columbia University, New York, NY, USA.

Department of Statistics, Columbia University, New York, NY, USA.

出版信息

Acta Oncol. 2020 Nov;59(11):1401-1408. doi: 10.1080/0284186X.2020.1787508. Epub 2020 Jul 1.

Abstract

BACKGROUND

There is currently no FDA or EMA-approved standard of care for metastatic uveal melanoma.

MATERIAL AND METHODS

A systematic review of all interventional uveal melanoma trials on the ClinicalTrials.gov database and EU Clinical Trials Register was conducted from January 15, 2019 through November 30, 2019. Categorical data analysis and descriptive statistics were generated.

RESULTS

A total of 119 trials met inclusion criteria for this systematic review, of which 39 were active. Of all trials, 47% were NIH-funded while 59% of active trials were industry funded. Of all trials, 86% were concerned with treatment of metastasis, 7% with adjuvant therapy, and 8% with treatment of primary tumor. In trials treating metastasis, 62% reported response rates as their primary outcome measure. Non-randomized patient allocation to treatment arms was reported in 73% of trials, and 8% of trials were in phase 3. Pharmaceutical drugs were utilized by 69% of trials. Of the 6 negative randomized trials, all reported no significant effect from intervention compared to a control arm and were usually initiated on preclinical or early phase data.

CONCLUSION

Given decreased NIH funding for uveal melanoma trials, clinicians should consider industry funding partnerships. Standardization of primary outcome measures between trials will also allow for statistical meta-analyses of results in this rare patient population. Finally, clinicians should use single arm studies to establish significant treatment response rates before proceeding with randomized trials.

摘要

背景

目前,转移性葡萄膜黑色素瘤既没有美国食品药品监督管理局(FDA)也没有欧洲药品管理局(EMA)批准的标准治疗方法。

材料与方法

我们对 ClinicalTrials.gov 数据库和欧盟临床试验注册中心的所有介入性葡萄膜黑色素瘤试验进行了系统回顾,检索时间为 2019 年 1 月 15 日至 2019 年 11 月 30 日。我们生成了分类数据分析和描述性统计数据。

结果

共有 119 项试验符合本系统综述的纳入标准,其中 39 项为正在进行的试验。在所有试验中,47%由美国国立卫生研究院资助,而 59%的正在进行的试验由工业界资助。在所有试验中,86%的试验涉及转移性疾病的治疗,7%的试验涉及辅助治疗,8%的试验涉及原发性肿瘤的治疗。在治疗转移性疾病的试验中,62%的试验报告以缓解率作为主要疗效评估指标。73%的试验报告了非随机患者分组到治疗组,8%的试验处于 3 期。69%的试验使用了药物治疗。在 6 项阴性随机试验中,所有试验均报告干预组与对照组相比没有显著效果,且这些试验通常是基于临床前或早期阶段的数据启动的。

结论

鉴于美国国立卫生研究院对葡萄膜黑色素瘤试验的资助减少,临床医生应考虑与工业界建立资助合作关系。试验之间主要疗效评估指标的标准化也将允许对这一罕见患者群体的结果进行统计学荟萃分析。最后,临床医生应该在进行随机试验之前,使用单臂研究来确定有意义的治疗反应率。

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