Critique of phase II agents for non-small cell lung cancer: what is our clinical need and which agents have potential?

IF 4.3 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Alessia Spagnuolo, Ilaria Spagnoletti, Emanuela Nuccio, Cesare Gridelli
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引用次数: 0

Abstract

Introduction: Phase II studies provide signals that guide therapeutic development for advanced NSCLC. This is particularly important for certain categories of patients, such as those who have already undergone immunotherapy and those with oncogene-addicted disease. However, promising results in phase II often do not translate into equally positive outcomes in phase III and the reason may be related to assay variability, sample heterogeneity, inadequate comparators or optimistic endpoints.

Areas covered: This paper provides an overview of treatments for advanced NSCLC and identifies settings where phase II evidence plays a decisive role: post-PD-(L)1/-chemotherapy, post-TKIs, frail patients or patients with brain disease. It also analyzes the reasons behind the failure of phase II success in phase III and proposes what makes a robust signal in phase II, while recognizing the limitations of surrogate endpoints. We take stock of the therapeutic classes that are gaining the most ground and provide a critical assessment of ongoing clinical programs.

Expert opinion: At present, a convincing phase II trial in NSCLC is possibly randomized, guided by biomarkers detected by standardized tests, with durable systemic and cerebral activity, inclusion of PROs, and is already in alignment with confirmatory study design and regulatory endpoints.

非小细胞肺癌II期药物的评论:我们的临床需要是什么,哪些药物有潜力?
II期研究提供了指导晚期NSCLC治疗发展的信号。这对某些类别的患者尤其重要,例如那些已经接受免疫治疗的患者和那些患有癌基因成瘾疾病的患者。然而,II期有希望的结果往往不能转化为III期同样积极的结果,原因可能与分析变异性、样本异质性、不充分的比较物或乐观的终点有关。涵盖领域:本文概述了晚期NSCLC的治疗方法,并确定了II期证据起决定性作用的环境:pd -(L)1/-化疗后、tkis后、体弱患者或脑疾病患者。它还分析了III期II期成功失败背后的原因,并提出了什么使II期信号具有鲁棒性,同时认识到代理端点的局限性。我们对取得最大进展的治疗类进行评估,并对正在进行的临床项目进行关键评估。专家意见:目前,一项令人信服的NSCLC II期试验可能是随机的,由标准化测试检测到的生物标志物引导,具有持久的全身和大脑活动,包括PROs,并且已经符合验证性研究设计和调节终点。
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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来源期刊
CiteScore
10.00
自引率
0.00%
发文量
71
审稿时长
6-12 weeks
期刊介绍: Expert Opinion on Investigational Drugs (ISSN 1354-3784 [print], 1744-7658 [electronic]) is a MEDLINE-indexed, peer-reviewed, international journal publishing review articles and original papers on drugs in preclinical and early stage clinical development, providing expert opinion on the scope for future development. The Editors welcome: Reviews covering preclinical through to Phase II data on drugs or drug classes for specific indications, and their potential impact on future treatment strategies Drug Evaluations reviewing the clinical and pharmacological data on a particular drug Original Research papers reporting the results of clinical investigations on agents that are in Phase I and II clinical trials The audience consists of scientists, managers and decision-makers in the pharmaceutical industry, and others closely involved in R&D.
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