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新型分子靶向个体化放射性药物的经济学评价

Economics of New Molecular Targeted Personalized Radiopharmaceuticals.

机构信息

Collider Accelerator Department, Brookhaven National Laboratory, Upton, NY.

出版信息

Semin Nucl Med. 2019 Sep;49(5):450-457. doi: 10.1053/j.semnuclmed.2019.07.002.

Abstract

Nuclear medicine has come a long way since 2007 when Adrian Nunn pointed out the approval of radiopharmaceuticals was at an all-time low with all the major radiopharmaceutical agents in use having been approved over 10 years ago. Challenges being the prohibitively high cost of drug development and the large number of drugs failing in clinical trials. Proceed to today where molecular imaging is fast-tracking the drug discovery process by reducing both the time and cost to screen candidates by quantitating the drugs effect on the target and toxicity to normal tissues. Nuclear medicine is now leading medical practice in personalized medicine using the theragnostic approach. Theragnostics is defined as the use of molecular diagnostic techniques in real time to stratify patients to guide treatment decisions such as the choice of drug, the dose of administration, and the timing of drug delivery for a given patient. Enabling visualization and quantitation of in vivo function of the whole body and thus patient heterogeneity and variability informs the physician on how to treat an individual patient. Recent successes such as the Food and Drug Administration approval of Lutathera and NETSPOT have resulted in an increasing number of pharmaceutical companies pursing theragnostics further heightened by the purchase of Advanced Accelerator Applications for 3.9 billion by Novartis and Endocyte, Inc for 2.1 billion. Theragnostics are further aiding drug development by showing which agents are most viable and reducing the overall cost of bringing a drug to clinical trials and regulatory approval. This is indeed a renaissance for nuclear medicine in which the acceptance of imaging to inform and monitor therapy has been embraced and even required by the Food and Drug Administration for the clinical evaluation of targeted therapeutic radiopharmaceuticals showing there is indeed a viable business model for targeted theragnostic radiopharmaceuticals and personalized medicine.

摘要

自 2007 年 Adrian Nunn 指出放射性药物的批准率处于历史最低点以来,核医学已经取得了长足的进步,所有正在使用的主要放射性药物制剂都是在 10 多年前获得批准的。面临的挑战是药物开发成本过高,以及大量药物在临床试验中失败。如今,分子成像技术通过定量评估药物对靶标的作用和对正常组织的毒性,加快了药物发现过程,从而缩短了筛选候选药物的时间和成本。核医学现在在个性化医学中处于领先地位,采用治疗诊断方法。治疗诊断被定义为实时使用分子诊断技术对患者进行分层,以指导治疗决策,例如选择药物、给药剂量以及给定患者的药物给药时间。它能够可视化和量化全身的体内功能,从而使医生了解如何治疗个体患者。最近的成功案例,如 Lutathera 和 NETSPOT 通过了美国食品和药物管理局的批准,促使越来越多的制药公司进一步追求治疗诊断,而诺华公司以 39 亿美元收购 Advanced Accelerator Applications 和 Endocyte, Inc 以 21 亿美元收购 Advanced Accelerator Applications 则进一步推动了这一趋势。治疗诊断通过显示哪些药物最可行,并降低将药物推向临床试验和监管批准的总体成本,进一步帮助药物开发。这确实是核医学的复兴,成像用于告知和监测治疗的接受程度已经被接受,甚至被美国食品和药物管理局要求用于靶向治疗放射性药物的临床评估,这表明靶向治疗诊断放射性药物和个性化医学确实存在可行的商业模式。

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