How can radiopharmaceutical therapies reach their full potential? Improving dose reporting and phase I clinical trial design Journal Article


Authors: Kiess, A. P.; O'Donoghue, J.; Uribe, C.; Bodei, L.; Hobbs, R. F.; Hesterman, J.; Kesner, A. L.; Sgouros, G.; on behalf of the RPT-TEC group
Article Title: How can radiopharmaceutical therapies reach their full potential? Improving dose reporting and phase I clinical trial design
Keywords: note; research design; methodology; antineoplastic agent; radiopharmaceuticals; neoplasm; neoplasms; nephrotoxicity; radiotherapy dosage; food and drug administration; prostate specific membrane antigen; myelodysplastic syndrome; radioactive iodine; biological activity; dosimetry; radiopharmaceutical agent; xerostomia; external beam radiotherapy; maximum tolerated dose; clinical trials, phase i as topic; adverse drug reaction; phase 1 clinical trial (topic); single photon emission computed tomography; acute myeloid leukemia; procedures; humans; human; xerophthalmia; vipivotide tetraxetan lutetium lu 177; oxodotreotide lutetium lu 177
Journal Title: Journal of Clinical Oncology
Volume: 42
Issue: 15
ISSN: 0732-183X
Publisher: American Society of Clinical Oncology  
Date Published: 2024-05-20
Start Page: 1734
End Page: 1737
Language: English
DOI: 10.1200/jco.23.01241
PUBMED: 38484205
PROVIDER: scopus
DOI/URL:
Notes: Note -- Source: Scopus
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  1. Lisa   Bodei
    205 Bodei
  2. Adam Leon Kesner
    68 Kesner