Abstract

To further verify the applicability of the micronuclei (MN) assay for clinical biodosimetry, we measured the MN yield in cytokinesis-blocked (CB) peripheral blood lymphocytes (PBL) of 12 patients with primary cancers of either prostate (n=9) or testis (n=3). These patients had no previous chemotherapy or radiotherapy (xRT). They were treated with standardized schemes of fractionated pelvic xRT. Before xRT, and at 1-3 random time-point during the course of xRT, blood samples were collected from each patient for the following purposes: (1) to assess the impact of pelvic xRT on the MN yield; and (2) to verify the relationship between the MN yield and the estimated equivalent (EQ) total-body absorbed dose. The number of xRT fractions,cumulative tumor doses, and EQ total-body absorbed doses of these patients represented in a wide range. We found that (1) before xRT, the mean(SD) yield of MN baseline level was 13.6 (6.9) per 1000 binucleated PBL. However, during the course of xRT (3-37 fractions), it increased to 84.3 (59.3). The ratio of relative increment of MN yield ranged from 0.9-17.0 folds above that of the respective baseline levels in each patient; and (2) MN yield (Y) increased with the estimated EQ dose (D) as Y=7.8+13.6D (r=0.8, p=0.0001). The distributions of MN yield were overdispersed in 11 patients, relative to dispersion expected under a Poisson model. Our findings indicate that the MN yield in CB PBL of cancer patients offers a reliable biodosimeter for EQ total-body absorbed radiation dose estimation.

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