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优化分子治疗的影像学方法。

Imaging approaches to optimize molecular therapies.

机构信息

Massachusetts General Hospital, Boston, MA 02114, USA.

Technical University Munich, Munich, Germany.

出版信息

Sci Transl Med. 2016 Sep 7;8(355):355ps16. doi: 10.1126/scitranslmed.aaf3936.

Abstract

Imaging, including its use for innovative tissue sampling, is slowly being recognized as playing a pivotal role in drug development, clinical trial design, and more effective delivery and monitoring of molecular therapies. The challenge is that, while a considerable number of new imaging technologies and new targeted tracers have been developed for cancer imaging in recent years, the technologies are neither evenly distributed nor evenly implemented. Furthermore, many imaging innovations are not validated and are not ready for widespread use in drug development or in clinical trial designs. Inconsistent and often erroneous use of terminology related to quantitative imaging biomarkers has also played a role in slowing their development and implementation. We examine opportunities for, and challenges of, the use of imaging biomarkers to facilitate development of molecular therapies and to accelerate progress in clinical trial design. In the future, in vivo molecular imaging, image-guided tissue sampling for mutational analyses ("high-content biopsies"), and noninvasive in vitro tests ("liquid biopsies") will likely be used in various combinations to provide the best possible monitoring and individualized treatment plans for cancer patients.

摘要

成像技术,包括其在创新组织采样中的应用,正逐渐被认为在药物开发、临床试验设计以及更有效的分子治疗药物的传递和监测方面发挥着关键作用。挑战在于,尽管近年来已经开发出了相当数量的用于癌症成像的新型成像技术和新型靶向示踪剂,但这些技术既没有得到均衡的分布,也没有得到均衡的应用。此外,许多成像创新技术尚未得到验证,也尚未准备好广泛应用于药物开发或临床试验设计。与定量成像生物标志物相关的术语的使用不一致且常常出现错误,这也对其发展和应用造成了阻碍。我们探讨了使用成像生物标志物来促进分子治疗药物的开发并加速临床试验设计进展的机会和挑战。在未来,体内分子成像、用于基因突变分析的图像引导组织采样(“高内涵活检”)以及非侵入性的体外检测(“液体活检”)可能会以各种组合方式用于为癌症患者提供最佳的监测和个体化治疗计划。

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