Dello Russo Cinzia, Navarra Pierluigi
Section of Pharmacology, Department of Healthcare Surveillance and Bioethics, Fondazione Policlinico Universitario A. Gemelli IRCCS, Università Cattolica Del Sacro Cuore, Rome, Italy.
MRC Centre for Drug Safety Science and Wolfson Centre for Personalized Medicine, Institute of Systems Molecular and Integrative Biology (ISMIB), University of Liverpool, Liverpool, United Kingdom.
Front Pharmacol. 2022 May 16;13:858354. doi: 10.3389/fphar.2022.858354. eCollection 2022.
Several drugs gained market authorization based on the demonstration of improved progression-free survival (PFS), adopted as a primary endpoint in Phase 3 clinical trials. In addition, an increasing number of drugs have been granted accelerated approval, and sometimes regular approval, by the main regulatory agencies based on the evaluation of the overall response rate in Phase 1 and 2 clinical trials. However, while the overall survival is an unbiased measure of drug efficacy, these outcomes rely on the assessment of radiological images and patients' categorization using standardized response criteria. The evaluation of these outcomes may be influenced by subjective factors, particularly when the analysis is performed locally. In fact, blinding of treatment is not always possible in modern oncology trials. Therefore, a blinded independent central review is often adopted to overcome the problem of expectation bias associated with local investigator assessments. In this regard, we have recently observed that local investigators tend to overestimate the overall response rate in comparison to central reviewers in Phase 2 clinical trials, whereas we did not find any significant evaluation bias between local investigators and central reviews when considering progression-free survival in both Phase 2 and 3 trials. In the present article, we have tried to understand the reasons behind this discrepancy by reviewing the available evidence in the literature. In addition, a further analysis of Phase 2 and 3 clinical trials that included the evaluation of both endpoints showed that local investigators significantly overestimate overall response rates compared to blinded independent central reviews in uncontrolled oncology trials.
几种药物基于无进展生存期(PFS)改善的证明获得了市场授权,无进展生存期在3期临床试验中被用作主要终点。此外,越来越多的药物已基于1期和2期临床试验中总体缓解率的评估,获得了主要监管机构的加速批准,有时是常规批准。然而,虽然总生存期是药物疗效的无偏倚衡量指标,但这些结果依赖于使用标准化反应标准对放射影像的评估和患者的分类。这些结果的评估可能受到主观因素的影响,尤其是在本地进行分析时。事实上,在现代肿瘤学试验中,治疗设盲并不总是可行的。因此,经常采用盲法独立中央审查来克服与本地研究者评估相关的期望偏倚问题。在这方面,我们最近观察到,在2期临床试验中,与中央审查者相比,本地研究者往往高估总体缓解率,而在考虑2期和3期试验中的无进展生存期时,我们未发现本地研究者与中央审查之间存在任何显著的评估偏倚。在本文中,我们试图通过回顾文献中的现有证据来理解这种差异背后的原因。此外,对包括两个终点评估的2期和3期临床试验的进一步分析表明,在非对照肿瘤学试验中,与盲法独立中央审查相比,本地研究者显著高估总体缓解率。