Clinical Trial Design and Endpoints for Stage IV Melanoma in the Modern Era

B. Izar, M. Regan, D. McDermott
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引用次数: 8

Abstract

Abstract Immunotherapies and targeted therapies for the treatment of metastatic or advanced melanoma produce unique patterns of antitumor response. Conventional outcome measures, such as median progression-free and overall survival, may not be ideally suited to identify all patients who derive a benefit from such therapies. Therefore, the introduction of additional endpoint measures, such as milestone comparisons, may be necessary to characterize the potential benefit of such treatment approaches. Immune checkpoint inhibitors induce durable responses in a portion of patients that may continue after treatment cessation. Measuring the associated treatment-free interval, treatment-free survival, and associated patient-reported outcomes could provide important information when implemented in prospective clinical trials. In this article, we discuss the limitations of current endpoint measures and the potential advantage of using novel endpoints and how these might be used in designing clinical trials to address critical unanswered questions for patients with metastatic melanoma.
现代IV期黑色素瘤的临床试验设计和终点
免疫疗法和靶向治疗用于治疗转移性或晚期黑色素瘤产生独特的抗肿瘤反应模式。传统的预后指标,如中位无进展期和总生存期,可能并不理想地适合于识别所有从此类治疗中获益的患者。因此,引入额外的终点测量,如里程碑比较,可能是必要的,以表征这种治疗方法的潜在益处。免疫检查点抑制剂在部分患者中诱导持久的反应,可能在治疗停止后继续。在前瞻性临床试验中,测量相关的无治疗间隔、无治疗生存期和相关的患者报告的结果可以提供重要的信息。在这篇文章中,我们讨论了当前终点测量的局限性和使用新终点的潜在优势,以及如何将这些终点用于设计临床试验,以解决转移性黑色素瘤患者的关键未解问题。
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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