Clarke Bonnie N
SNMMI, United States.
J Nucl Med Technol. 2018 Feb 2. doi: 10.2967/jnmt.117.205021.
The field of molecular imaging is undergoing a period of growth and expansion. Of the ten FDA-approved PET imaging agents, six have been approved since 2012. As we enter 2018, we await the approval of a targeted radionuclide therapy, Lu-DOTATATE. The approval of agents such as C-choline represented a paradigm shift in radiopharmaceutical drug development. This shift has illuminated a path to approval for similar agents and demonstrated the importance of molecular imaging in determining effective treatment strategies in serious diseases. This is a review of approval history of PET agents with a summary of how to use the newest agents in your clinic. Then, a look to the not-so-distant future to see what agents we may be using to image and treat patients with serious illnesses. The promise of personalized medicine is within our grasp.
分子成像领域正处于一个发展和扩张的时期。在FDA批准的十种PET成像剂中,自2012年以来已有六种获得批准。随着我们进入2018年,我们正在等待一种靶向放射性核素疗法——镥[177Lu]奥曲肽的批准。像碳-11胆碱这样的药物的批准代表了放射性药物开发的一个范式转变。这一转变为类似药物的批准指明了道路,并证明了分子成像在确定严重疾病有效治疗策略中的重要性。本文回顾了PET药物的批准历史,并总结了如何在临床中使用最新的药物。然后,展望不远的将来,看看我们可能会使用哪些药物来对重症患者进行成像和治疗。个性化医疗的前景已触手可及。