Comparative evaluation of radionuclide therapy using 90Y and 177Lu
Objective Both 90 Y and 177 Lu are attractive β-emitters for radionuclide therapy and have been used in clinical practice. Nevertheless, comparative evaluation between 90 Y- and 177 Lu-labeled molecules has not been fully conducted. Thus, in this study, the features of 90 Y and 177 Lu for radionucli...
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Published in: | Annals of nuclear medicine Vol. 37; no. 1; pp. 52 - 59 |
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Main Authors: | , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Singapore
Springer Nature Singapore
2023
Springer Nature B.V |
Subjects: | |
Online Access: | Get full text |
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Summary: | Objective
Both
90
Y and
177
Lu are attractive β-emitters for radionuclide therapy and have been used in clinical practice. Nevertheless, comparative evaluation between
90
Y- and
177
Lu-labeled molecules has not been fully conducted. Thus, in this study, the features of
90
Y and
177
Lu for radionuclide therapy were assessed in tumor-bearing mice.
Methods
Two tumor cell lines with different growth rates were used. Biodistribution studies of
177
Lu-labeled antibodies (
177
Lu-Abs) were conducted in each tumor-bearing mouse model. Subsequently, the therapeutic effect of
90
Y- and
177
Lu-Ab were assessed in tumor-bearing mice. The absorbed radiation dose for the tumor was estimated using the Monte Carlo simulation.
Results
177
Lu-Abs demonstrated high tumor accumulation in both tumor-xerograph. In the fast-growing tumor model,
90
Y-Ab showed a better therapeutic effect than
177
Lu-Ab, reflecting a higher absorbed radiation dose of
90
Y-Ab than that of
177
Lu-Ab. In the slow-growing tumor model, both
90
Y- and
177
Lu-Ab showed an excellent therapeutic effect; however,
177
Lu-Ab had a longer efficacy period than
90
Y-Ab, which could be attributed to the longer half-life and better dose uniformity of
177
Lu than those of
90
Y.
Conclusions
To accomplish a maximum therapeutic effect, selecting
90
Y or
177
Lu, to depend on the growth rate of individual cancer, would be helpful. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0914-7187 1864-6433 |
DOI: | 10.1007/s12149-022-01803-y |