Leveraging Programmatic Collaboration for a Radiopharmaceutical Clinic

Author:

Kunos Charles A.1,Martin Molly E.2,Georgiou Michalis F.3,Kuker Russ A.3ORCID,Chauhan Aman4

Affiliation:

1. Department of Radiation Oncology, Sylvester Comprehensive Cancer Center, 1475 NW 12th Avenue, Suite 1500, Miami, FL 33136, USA

2. Department of Radiology, Division of Nuclear Medicine, University of Iowa Health Care, Iowa City, IA 52242, USA

3. Department of Radiology, Division of Nuclear Medicine, University of Miami, Miami, FL 33136, USA

4. Department of Medicine, Division of Medical Oncology, University of Miami, Miami, FL 33136, USA

Abstract

Radiation oncologists, radiopharmacists, nuclear medicine physicians, and medical oncologists have seen a renewed clinical interest in radiopharmaceuticals for the curative or the palliative treatment of cancer. To allow for the discovery and the clinical advancement of targeted radiopharmaceuticals, these stakeholders have reformed their trial efforts and remodeled their facilities to accommodate the obligations of a program centered upon radioactive investigational drug products. Now considered informally as drugs and not beam radiotherapy, radiopharmaceuticals can be more easily studied in the traditional clinical trial enterprise ranging from phase 0–I to phase III studies. Resources and physical facilities allocated to radiopharmaceuticals have brought forth new logistics and patient experience for safe and satisfactory drug delivery. The clinical use of theranostic agents—that is, diagnostic and therapeutic radionuclide pairs—has accelerated radiopharmaceutical development.

Funder

NCI

Publisher

MDPI AG

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