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: | , , , , , , , |
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Abstract | 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. |
---|---|
AbstractList | OBJECTIVEBoth 90Y and 177Lu are attractive β-emitters for radionuclide therapy and have been used in clinical practice. Nevertheless, comparative evaluation between 90Y- and 177Lu-labeled molecules has not been fully conducted. Thus, in this study, the features of 90Y and 177Lu for radionuclide therapy were assessed in tumor-bearing mice. METHODSTwo tumor cell lines with different growth rates were used. Biodistribution studies of 177Lu-labeled antibodies (177Lu-Abs) were conducted in each tumor-bearing mouse model. Subsequently, the therapeutic effect of 90Y- and 177Lu-Ab were assessed in tumor-bearing mice. The absorbed radiation dose for the tumor was estimated using the Monte Carlo simulation. RESULTS177Lu-Abs demonstrated high tumor accumulation in both tumor-xerograph. In the fast-growing tumor model, 90Y-Ab showed a better therapeutic effect than 177Lu-Ab, reflecting a higher absorbed radiation dose of 90Y-Ab than that of 177Lu-Ab. In the slow-growing tumor model, both 90Y- and 177Lu-Ab showed an excellent therapeutic effect; however, 177Lu-Ab had a longer efficacy period than 90Y-Ab, which could be attributed to the longer half-life and better dose uniformity of 177Lu than those of 90Y. CONCLUSIONSTo accomplish a maximum therapeutic effect, selecting 90Y or 177Lu, to depend on the growth rate of individual cancer, would be helpful. 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. |
Author | Endo, Keigo Matsumoto, Shojiro Hashimoto, Kazuyuki Sakashita, Tetsuya Watanabe, Satoshi Ishioka, Noriko S. Watanabe, Shigeki Hanaoka, Hirofumi |
Author_xml | – sequence: 1 givenname: Hirofumi orcidid: 0000-0003-2421-7397 surname: Hanaoka fullname: Hanaoka, Hirofumi email: hanaokah@gunma-u.ac.jp organization: Gunma University Graduate School of Medicine – sequence: 2 givenname: Kazuyuki surname: Hashimoto fullname: Hashimoto, Kazuyuki organization: Quantum Beam Science Center, Japan Atomic Energy Agency – sequence: 3 givenname: Satoshi surname: Watanabe fullname: Watanabe, Satoshi organization: Quantum Beam Science Research Directorate, National Institute for Quantum Science and Technology – sequence: 4 givenname: Shojiro surname: Matsumoto fullname: Matsumoto, Shojiro organization: Quantum Beam Science Research Directorate, National Institute for Quantum Science and Technology – sequence: 5 givenname: Tetsuya surname: Sakashita fullname: Sakashita, Tetsuya organization: Quantum Beam Science Research Directorate, National Institute for Quantum Science and Technology – sequence: 6 givenname: Shigeki surname: Watanabe fullname: Watanabe, Shigeki organization: Quantum Beam Science Research Directorate, National Institute for Quantum Science and Technology – sequence: 7 givenname: Noriko S. surname: Ishioka fullname: Ishioka, Noriko S. organization: Quantum Beam Science Research Directorate, National Institute for Quantum Science and Technology – sequence: 8 givenname: Keigo surname: Endo fullname: Endo, Keigo organization: Gunma University Graduate School of Medicine |
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Cites_doi | 10.18632/oncotarget.24524 10.2967/jnumed.118.218917 10.1021/acs.molpharmaceut.8b00027 10.2967/jnumed.116.186767 10.3390/cancers14010129 10.1016/j.apradiso.2017.07.028 10.1007/s00259-011-1833-x 10.1200/JCO.22.00176 10.1007/s12282-018-0834-z 10.3934/mbe.2022190 10.1038/nrc3925 10.1007/s10967-014-3534-y 10.1016/j.esmoop.2021.100171 10.1007/s12149-017-1197-9 10.2147/OTT.S97584 10.1186/s13073-021-00940-9 10.1007/s12149-020-01548-6 10.1007/s11523-014-0324-y 10.31661/jbpe.v0i0.2101-1256 |
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Snippet | Objective
Both
90
Y and
177
Lu are attractive β-emitters for radionuclide therapy and have been used in clinical practice. Nevertheless, comparative evaluation... ObjectiveBoth 90Y and 177Lu are attractive β-emitters for radionuclide therapy and have been used in clinical practice. Nevertheless, comparative evaluation... OBJECTIVEBoth 90Y and 177Lu are attractive β-emitters for radionuclide therapy and have been used in clinical practice. Nevertheless, comparative evaluation... |
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SubjectTerms | Antibodies Emitters Evaluation Growth rate Half-life Imaging Lutetium isotopes Medicine Medicine & Public Health Monte Carlo simulation Nuclear Medicine Original Article Radiation Radiation dosage Radiation therapy Radioisotopes Radiology Tumor cell lines Tumors Yttrium isotopes |
Title | Comparative evaluation of radionuclide therapy using 90Y and 177Lu |
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