Dosimetric evaluation of 153Sm-EDTMP, 177Lu-EDTMP and 166Ho-EDTMP for systemic radiation therapy: Influence of type and energy of radiation and half-life of radionuclides
- 1. Radiopharmaceutical Research and Development Lab (RRDL), Nuclear Science and Technology, Research Institute (NSTRI), P.O. Box 14395-836 Tehran (Iran, Islamic Republic of)
- 2. Research Institute for Nuclear Medicine, Tehran University of Medical Sciences, Tehran (Iran, Islamic Republic of)
Description
In radiopharmaceutical therapy, delivered doses to critical organs must be below a certain threshold therefore internal radiation dosimetry of radiopharmaceuticals is essential. Advantages and disadvantages of radionuclides with different characteristics were evaluated for selection of appropriate radionuclide. The Monte Carlo MCNPX simulation program was used to obtain radial dose and cumulative dose of 153Sm, 177Lu and 166Ho used in radiotherapy of bone metastases. A cylindrical geometry with constant density materials was supposed for simulation of femur bone. The radius of bone marrow, bone, and surrounding soft tissue was considered 0.6 cm, 1.3 cm and 4 cm, respectively. It was assumed that the radionuclides were uniformly distributed throughout the tumor. “continuous energy spectrum” of beta particle was used instead of mean beta energy. Our simulations show that absorbed dose in target organ (bone) is greater than other organs and 166Ho gives a higher dose to the critical organ of bone marrow than either 153Sm or 177Lu. Absorbed dose versus time demonstrate faster dose delivery for the short half-life radionuclides (153Sm and 166Ho). These results are in good agreement with clinical observations which show a pain relief within 1 week after intravenous administration of 153Sm-EDTMP, whereas it occurs within 2 week in the case of 177Lu-EDTMP. According to the results, combination of different radionuclides with different characteristics such as 153Sm-EDTMP and 177Lu-EDTMP could be more advantageous to patients with painful bone metastasis. - Highlights: • The radial dose and cumulative dose of 153Sm, 177Lu and 166Ho are calculated. • The effect of half-life of the radionuclide on the suitable activity for injection is studied. • Dose delivery is fast for the short half-life radionuclides (153Sm and 166Ho). • The results are in good accordance with clinical observations. • The combination of different radionuclides with different characteristics could be more advantageous
Availability note (English)
Available from http://dx.doi.org/10.1016/j.radphyschem.2014.11.015Additional details
Identifiers
- DOI
- 10.1016/j.radphyschem.2014.11.015;
- PII
- S0969-806X(14)00427-7;
Publishing Information
- Journal Title
- Radiation Physics and Chemistry (1993)
- Journal Volume
- 108
- Journal Page Range
- p. 60-64
- ISSN
- 0969-806X
- CODEN
- RPCHDM
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 46124445
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- ABSORBED RADIATION DOSES; BETA PARTICLES; BONE MARROW; COMPUTERIZED SIMULATION; CRITICAL ORGANS; CYLINDRICAL CONFIGURATION; DOSIMETRY; ENERGY SPECTRA; FEMUR; HALF-LIFE; HOLMIUM 166; LUTETIUM 177; METASTASES; MONTE CARLO METHOD; NEOPLASMS; PATIENTS; RADIATION DOSE DISTRIBUTIONS; RADIOPHARMACEUTICALS; RADIOTHERAPY; SAMARIUM 153
- Descriptors DEC
- ANIMAL TISSUES; BETA DECAY RADIOISOTOPES; BETA-MINUS DECAY RADIOISOTOPES; BODY; CALCULATION METHODS; CHARGED PARTICLES; CONFIGURATION; DAYS LIVING RADIOISOTOPES; DISEASES; DOSES; DRUGS; EVEN-ODD NUCLEI; HEMATOPOIETIC SYSTEM; HOLMIUM ISOTOPES; INTERMEDIATE MASS NUCLEI; IONIZING RADIATIONS; ISOMERIC TRANSITION ISOTOPES; ISOTOPES; LABELLED COMPOUNDS; LUTETIUM ISOTOPES; MATERIALS; MEDICINE; NUCLEAR MEDICINE; NUCLEI; ODD-EVEN NUCLEI; ODD-ODD NUCLEI; ORGANS; RADIATION DOSES; RADIATIONS; RADIOACTIVE MATERIALS; RADIOISOTOPES; RADIOLOGY; RARE EARTH NUCLEI; SAMARIUM ISOTOPES; SIMULATION; SKELETON; SPECTRA; THERAPY; YEARS LIVING RADIOISOTOPES
Optional Information
- Copyright
- Copyright (c) 2014 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.