The Landmark Series: The Future of Pancreatic Cancer Clinical Trials.

IF 3.4 2区 医学 Q2 ONCOLOGY
Annals of Surgical Oncology Pub Date : 2025-04-01 Epub Date: 2025-01-15 DOI:10.1245/s10434-024-16840-2
Yongwoo David Seo, Matthew H G Katz, Rebecca A Snyder
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引用次数: 0

Abstract

Pancreatic cancer has a poor prognosis despite ongoing advances in systemic and multimodal therapies. This review analyzes recent progress and future directions in pancreatic cancer clinical trials, emphasizing the evolution from traditional approaches to a more personalized and biologically-driven treatment paradigm. While improvements in overall survival have been achieved through perioperative therapies, gaps remain in our understanding of optimal treatment strategies. Key questions include selection of specific chemotherapeutic agents, duration of preoperative therapy, the role of radiotherapy, and accurate and real-time assessment of response to therapy. Historically, pancreatic cancer clinical trials have been designed based on anatomic criteria, failing to account for the inherent biologic heterogeneity of this disease. The field is now moving towards a precision oncology approach, leveraging genomic and transcriptomic data to identify predictive biomarkers and personalize treatment selection. Novel clinical trial designs, such as platform and basket trials, are accelerating the evaluation of new therapeutic strategies and facilitating efficient patient selection, particularly in the context of new emerging targeted therapies such as KRAS inhibitors. Furthermore, implementation of dynamic response assessment techniques, such as circulating tumor DNA and radiomics, may inform treatment decision-making and improve prediction of long-term outcomes. By integrating these evolving strategies, the emerging clinical trial landscape has the potential to transform the treatment of pancreatic cancer and yield meaningful improvements in patient outcomes.

里程碑系列:胰腺癌临床试验的未来。
尽管系统和多模式治疗不断取得进展,但胰腺癌预后较差。本文分析了胰腺癌临床试验的最新进展和未来方向,强调了从传统方法到更加个性化和生物驱动的治疗范式的演变。虽然通过围手术期治疗可以提高总生存率,但我们对最佳治疗策略的理解仍然存在差距。关键问题包括特异性化疗药物的选择、术前治疗的持续时间、放疗的作用以及对治疗反应的准确和实时评估。从历史上看,胰腺癌临床试验是基于解剖学标准设计的,未能考虑到这种疾病固有的生物学异质性。该领域现在正朝着精确肿瘤学的方向发展,利用基因组和转录组学数据来识别预测性生物标志物和个性化治疗选择。新的临床试验设计,如平台和篮子试验,正在加速对新治疗策略的评估,促进有效的患者选择,特别是在新兴的靶向治疗(如KRAS抑制剂)的背景下。此外,动态反应评估技术的实施,如循环肿瘤DNA和放射组学,可以为治疗决策提供信息,并改善对长期结果的预测。通过整合这些不断发展的策略,新兴的临床试验前景有可能改变胰腺癌的治疗方法,并对患者的预后产生有意义的改善。
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
5.90
自引率
10.80%
发文量
1698
审稿时长
2.8 months
期刊介绍: The Annals of Surgical Oncology is the official journal of The Society of Surgical Oncology and is published for the Society by Springer. The Annals publishes original and educational manuscripts about oncology for surgeons from all specialities in academic and community settings.
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