265
Views
10
CrossRef citations to date
0
Altmetric
Original Articles

Comparative studies on the potential use of 177Lu-based radiopharmaceuticals for the palliative therapy of bone metastases

ORCID Icon, ORCID Icon, & ORCID Icon
Pages 779-789 | Received 11 Jun 2019, Accepted 13 Jan 2020, Published online: 03 Mar 2020
 

Abstract

Purpose: In recent years, radionuclides like 177Lu have been considered promising material for the creation of therapeutic radiopharmaceuticals. With the therapeutic use of radiopharmaceuticals, the absorbed doses per tumor may exceed 10 Gy. It is extremely important that doses absorbed by healthy organs and tissues do not exceed the threshold for the incidence of deterministic effects.

Materials and methods: The potential use of the radionuclide lutetium-177 for the palliative treatment of pain in bone metastases is analyzed. The radionuclide 177Lu is a beta-emitting nuclide with a maximal energy of 0.49 MeV and a half-life of 6.6 days (161 h). Two therapeutic agents were considered: methylene diphosphonate (MDP) and ethylenediamine tetramethylene phosphonic acid (EDTMP). Both drugs contain phosphorus compounds in their composition, which ensures high tropism in bone tissue. For both drugs, biokinetic models of 177Lu’s behavior in the human body are created. A number of studies have shown that the radiochemical stability of these drugs is about 99%: these calculations took into account the presence of a free 177Lu radionuclide in each solution. The absorbed doses in organs and tissues when using the radiopharmaceuticals 177Lu-MDP and 177Lu-EDTMP, as well as the currently used drugs 153Sm-EDTMP and 89SrCl2, are compared. In order to assess the risk of the patient’s exposure to a radiopharmaceutical, the absorbed doses are calculated for each organ where the radioactive label is mainly deposited: the kidneys, red bone marrow, liver and bone surface.

Results: The intensity of dose accumulation when using different drugs on the pathological focus is different. The drug 177Lu-MDP is faster than other drugs when it comes to the full realization of the expected dose; therefore, a therapeutic effect is achieved faster when it is used. The slowest absorbed dose accumulates when strontium chloride is used. To compare the effectiveness of preparations based on the 177Lu radionuclide, an analysis of the radiopharmaceuticals currently used for the palliative therapy of bone metastases (89SrCl2 and 153Sm-EDTMP) was performed. For 89Sr, the most vulnerable organs are the kidneys, red bone marrow and liver, while for 153Sm-EDTMP, red marrow bone is most vulnerable. For radiopharmaceuticals based on the 177Lu radionuclide, the most vulnerable organs are the kidneys, liver and red bone marrow. This proves the effectiveness of the 177Lu-MDP and 177Lu-EDTMP radiopharmaceuticals.

Conclusions: According to the results of the calculations, 177Lu-EDTMP and 177Lu-MDP demonstrate the best results for the palliative therapy of bone metastases.

Disclosure statement

No potential conflict of interest was reported by the author(s).

Additional information

Notes on contributors

Hesham M. H. Zakaly

Hesham M.H. Zakaly is currently pursuing PhD degree program in radiation physics in Ural Federal University, Russia, assistant lecture at Physics Department, Faculty of Science, Al-Azhar University, Assuit Branch, 71524 Assuit, Egypt, E-mail: [email protected]

Mostafa Y. A. Mostafa

Mostafa Y.A. Mostafa is currently pursuing PhD degree program in radiation physics in Ural Federal University, Russia, PH-+79827122964. assistant lecture at Minia University, Faculty of Science, Department of Physics, El-Minia, Egypt, E-mail: [email protected]

Darya Deryabina

Darya Deryabina, was finished Bsc degree in physics 2 years ago in Ural Federal University, Russia.

Michael Zhukovsky

Michael Zhukovsky professor of radiation physics Ural Federal University, directorate of Institute of Industrial Ecology-Ural Branch of RAS-Ekaterinburg, Russia.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.