DNA damage in blood leucocytes of prostate cancer patients during therapy with <sup>177</sup>Lu-PSMA.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 31028426.
- Also identified by DOI 10.1007/s00259-019-04317-4 and PMC identifier 6584247.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
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 <sup>177</sup>Lu-PSMA. Blood samples from 16 prostate cancer patients receiving their first <sup>177</sup>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. 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<sup>2</sup> = 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<sup>2</sup> = 0.56). In most patients, DNA DSBs were repaired effectively. However, in some patients RIF did not disappear completely even 96 h after administration. The general pattern of the time- and dose-dependent induction and disappearance of RIF during <sup>177</sup>Lu-PSMA therapy is similar to that of other radionuclide therapies.
Medical subject headings
- DNA Damage
- Dipeptides
- Heterocyclic Compounds, 1-Ring
- Leukocytes
- Prostatic Neoplasms
- Radiopharmaceuticals