The evolution of precision oncology: The ongoing impact of the Drug Rediscovery Protocol (DRUP).

IF 2.7 3区 医学 Q3 ONCOLOGY
Soemeya F Haj Mohammad, Hans J L Timmer, Laurien J Zeverijn, Birgit S Geurts, Ilse A C Spiekman, Karlijn Verkerk, Florentine A J Verbeek, Henk M W Verheul, Emile E Voest, Hans Gelderblom
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引用次数: 0

Abstract

Background and purpose: The Drug Rediscovery Protocol (DRUP) is a Dutch, pan-cancer, nonrandomized clinical trial that aims to investigate the efficacy and safety of targeted and immunotherapies outside their registered indication in patients with advanced or metastatic cancer.

Patients: Patients with advanced or metastatic cancer are eligible when there are no standard of care treatment options left and the tumor possesses a molecular genomic variant for which commercially available anticancer treatment is accessible off-label in DRUP. Clinical benefit is the study's primary endpoint, characterized by a confirmed objective response or stable disease after at least 16 weeks of treatment.

Results: More than 2,500 patients have undergone evaluation, of which over 1,500 have started treatment in DRUP. The overall clinical benefit rate (CBR) remains 33%. The nivolumab cohort for patients with microsatellite instable metastatic tumors proved highly successful with a CBR of 63%, while palbociclib or ribociclib in patients with tumors harboring CDK4/6 pathway alterations showed limited efficacy, with a CBR of 15%. The formation of two European initiatives (PCM4EU and PRIME-ROSE) strives to accelerate implementation and enhance data collection to broaden equitable access to anticancer treatments and gather more evidence.

Conclusion: DRUP persists in improving patients access to off-label targeted or immunotherapy in the Netherlands and beyond. The expansion of DRUP-like clinical trials across Europe provides countless opportunities for broadening the horizon of precision oncology.

精准肿瘤学的演变:药物再发现方案(DRUP)的持续影响。
背景和目的:药物再发现方案(DRUP)是荷兰的一项泛癌症非随机临床试验,旨在研究晚期或转移性癌症患者在注册适应症之外接受靶向治疗和免疫治疗的疗效和安全性:晚期或转移性癌症患者:如果没有标准治疗方案可供选择,且肿瘤具有分子基因组变异,在 DRUP 的标签外可以接受市售抗癌治疗,则符合条件。临床获益是该研究的主要终点,其特征是经过至少 16 周的治疗后确认客观反应或病情稳定:结果:2500 多名患者接受了评估,其中 1500 多名已开始接受 DRUP 治疗。总体临床获益率(CBR)仍为33%。针对微卫星不稳定性转移性肿瘤患者的 nivolumab 队列证明非常成功,CBR 为 63%,而针对携带 CDK4/6 通路改变的肿瘤患者的 palbociclib 或 ribociclib 的疗效有限,CBR 为 15%。两个欧洲倡议(PCM4EU 和 PRIME-ROSE)的形成旨在加快实施并加强数据收集,以扩大抗癌治疗的公平可及性并收集更多证据:结论:在荷兰及其他国家,DRUP 一直在改善患者接受标签外靶向或免疫疗法的机会。类似 DRUP 的临床试验在欧洲的推广为扩大精准肿瘤学的视野提供了无数机会。
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
Acta Oncologica
Acta Oncologica 医学-肿瘤学
CiteScore
4.30
自引率
3.20%
发文量
301
审稿时长
3 months
期刊介绍: Acta Oncologica is a journal for the clinical oncologist and accepts articles within all fields of clinical cancer research. Articles on tumour pathology, experimental oncology, radiobiology, cancer epidemiology and medical radio physics are also welcome, especially if they have a clinical aim or interest. Scientific articles on cancer nursing and psychological or social aspects of cancer are also welcomed. Extensive material may be published as Supplements, for which special conditions apply.
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