Published September 17, 2021
| Version v1
Journal article
Safety and efficacy of peptide receptor radionuclide therapy with 177Lu-DOTA0-Tyr3-octreotate in combination with amino acid solution infusion in Japanese patients with somatostatin receptor-positive, progressive neuroendocrine tumors
- 1. Yokohama City University, Graduate School of Medicine. Department of Oncology, Oncology Division, Yokohama, Kanagawa (Japan)
- 2. Yokohama City University, Graduate School of Medicine. Department of Radiation Oncology, Yokohama, Kanagawa (Japan)
- 3. Yokohama City University, Graduate School of Medicine. Department of Radiology, Yokohama, Kanagawa (Japan)
Description
Purpose
Peptide receptor radionuclide therapy (PRRT) with 177Lu-DOTA0-Tyr3-octreotate (177Lu-DOTATATE) is one of the most reliable treatments for unresectable, progressive neuroendocrine tumors (NETs) with somatostatin receptor expression. We have, for the first time, reported the results of the tolerability, safety, pharmacokinetics, dosimetry, and efficacy of this treatment for Japanese patients with NET.Methods
Patients with unresectable, somatostatin receptor scintigraphy (SRS)-positive NETs were enrolled in this phase I clinical trial. They were treated with 29.6 GBq of 177Lu-DOTATATE (four doses of 7.4 GBq) combined with amino acid solution infusion plus octreotide long-acting release (LAR) 30 mg. The primary objective of this study was to evaluate the tolerability, safety, pharmacokinetics, and dosimetry of a single administration of this treatment in patients with SRS-positive NETs.Results
Six Japanese patients (three men and three women; mean age 61.5 years; range 50-70 years) with SRS-positive unresectable NETs were recruited. 177Lu-DOTATATE was eliminated from the blood in a two-phase manner. Cumulative urinary excretion of radioactivity was 60.1% (range 49.0%-69.8%) within the initial 6 h. The cumulative renal absorbed dose for 29.6 GBq of 177Lu-DOTATATE was 16.8 Gy (range 12.0-21.2 Gy), and the biological effective dose was 17.0 Gy (range 12.2-21.5 Gy). Administration of 177Lu-DOTATATE was well tolerated, with no dose-limiting toxicities. Grade 3 lymphopenia occurred in two (33.3%) cases, but there were no other severe toxicities. Four patients achieved partial response (objective response rate, 66.7%), one patient had stable disease, and one patient had progressive disease.Conclusion
PRRT with 177Lu-DOTATATE was well-tolerated and showed good outcomes in Japanese patients with unresectable NETs. Peptide receptor radionuclide therapy, 177Lu-DOTA0-Tyr3-octreotate. (author)Additional details
Identifiers
Publishing Information
- Journal Title
- Annals of Nuclear Medicine
- Journal Volume
- 35
- Journal Issue
- 12
- Journal Page Range
- p. 1332-1341
- ISSN
- 0914-7187
- CODEN
- ANMEEX
INIS
- Country of Publication
- Japan
- Country of Input or Organization
- Japan
- INIS RN
- 54066244
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- AMINO ACIDS; ENDOCRINE GLANDS; LUTETIUM 177; NEOPLASMS; NERVE CELLS; PATIENTS; PEPTIDES; RADIOTHERAPY; RECEPTORS; SOMATOSTATIN
- Descriptors DEC
- ANIMAL CELLS; BETA DECAY RADIOISOTOPES; BETA-MINUS DECAY RADIOISOTOPES; BODY; CARBOXYLIC ACIDS; DAYS LIVING RADIOISOTOPES; DISEASES; GLANDS; INTERMEDIATE MASS NUCLEI; ISOMERIC TRANSITION ISOTOPES; ISOTOPES; LUTETIUM ISOTOPES; MEDICINE; MEMBRANE PROTEINS; NUCLEAR MEDICINE; NUCLEI; ODD-EVEN NUCLEI; ORGANIC ACIDS; ORGANIC COMPOUNDS; ORGANS; PROTEINS; RADIOISOTOPES; RADIOLOGY; RARE EARTH NUCLEI; SOMATIC CELLS; THERAPY
Optional Information
- Copyright
- Copyright (c) 2021 © The Author(s) 2021