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90Y/177Lu-DOTATOC: From Preclinical Studies to Application in Humans
Licia Uccelli1,2, Alessandra Boschi3, Corrado Cittanti1,2
1Department of Translational Medicine, University of Ferrara, 44121 Ferrara, Italy.
Pharmaceutics
|September 28, 2021
Summary
Peptide Receptor Radionuclide Therapy (PRRT) offers a promising treatment for neuroendocrine tumors (NETs), showing comparable survival rates to standard therapies. This review highlights the success of [90Y]Y-DOTATOC and [177Lu]Lu-DOTATOC in PRRT.
Area of Science:
- Oncology
- Nuclear Medicine
- Radiopharmaceutical Therapy
Background:
- Neuroendocrine tumors (NETs) often present as inoperable or metastatic.
- Standard therapies for NETs have limitations in efficacy and side effect profiles.
- Peptide Receptor Radionuclide Therapy (PRRT) has emerged as a significant treatment modality.
Purpose of the Study:
- To review the characteristics and performance of [90Y]Y-DOTATOC and [177Lu]Lu-DOTATOC.
- To summarize the key literature findings over 25 years regarding these radiopharmaceuticals.
- To trace the progression of these therapies from preclinical research to clinical application.
Main Methods:
- Literature review covering 25 years of research on PRRT for NETs.
- Analysis of studies focusing on [90Y]Y-DOTATOC and [177Lu]DOTATOC.
- Evaluation of progression-free survival (PFS) and overall survival (OS) data.
Main Results:
- PRRT demonstrates favorable progression-free survival (PFS) and overall survival (OS) for NET patients.
- [90Y]Y-DOTATOC and [177Lu]Lu-DOTATOC are the most utilized radiopharmaceuticals in NET PRRT.
- Significant results from preclinical and clinical studies support the efficacy of these agents.
Conclusions:
- PRRT using [90Y]Y-DOTATOC and [177Lu]Lu-DOTATOC is an effective treatment for inoperable or metastatic NETs.
- These radiopharmaceuticals have successfully transitioned from research to clinical practice.
- Continued research and application of PRRT are crucial for improving NET patient outcomes.

