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DNA damage in blood leucocytes of prostate cancer patients during therapy with 177 Lu-PSMA.

Authors :
Schumann S
Scherthan H
Lapa C
Serfling S
Muhtadi R
Lassmann M
Eberlein U
Source :
European journal of nuclear medicine and molecular imaging [Eur J Nucl Med Mol Imaging] 2019 Jul; Vol. 46 (8), pp. 1723-1732. Date of Electronic Publication: 2019 Apr 27.
Publication Year :
2019

Abstract

Purpose: The aim of this study was to investigate the time- and dose-dependency of DNA double-strand break (DSB) induction and repair in peripheral blood leucocytes of prostate cancer patients during therapy with <superscript>177</superscript> Lu-PSMA.<br />Methods: Blood samples from 16 prostate cancer patients receiving their first <superscript>177</superscript> Lu-PSMA therapy were taken before and at seven time-points (between 1 h and 96 h) after radionuclide administration. Absorbed doses to the blood were calculated using integrated time-activity curves of the blood and the whole-body. For DSB quantification, leucocytes were isolated, fixed in ethanol and immunostained with γ-H2AX and 53BP1 antibodies. Colocalizing foci of both DSB markers were manually counted in a fluorescence microscope.<br />Results: The average number of radiation-induced foci (RIF) per cell increased within the first 4 h after administration, followed by a decrease indicating DNA repair. The number of RIF during the first 2.6 h correlated linearly with the absorbed dose to the blood (R <superscript>2</superscript>  = 0.58), in good agreement with previously published in-vitro data. At late time-points (48 h and 96 h after administration), the number of RIF correlated linearly with the absorbed dose rate (R <superscript>2</superscript>  = 0.56). In most patients, DNA DSBs were repaired effectively. However, in some patients RIF did not disappear completely even 96 h after administration.<br />Conclusion: The general pattern of the time- and dose-dependent induction and disappearance of RIF during <superscript>177</superscript> Lu-PSMA therapy is similar to that of other radionuclide therapies.

Details

Language :
English
ISSN :
1619-7089
Volume :
46
Issue :
8
Database :
MEDLINE
Journal :
European journal of nuclear medicine and molecular imaging
Publication Type :
Academic Journal
Accession number :
31028426
Full Text :
https://doi.org/10.1007/s00259-019-04317-4