Of the 255 patients enrolled, a total of 237 (92.9%) men at screening and 213 (83.5%) at cycle 2 had evaluable samples. Over 80% of patients had detectable CTCs ³ 1 at both time points in time (median 4.1 at screening and 5.2 at cycle 2), and the number of CTCs correlated with other serum measurements, including lactate dehydrogenase, alkaline phosphatase, and prostate-specific antigen. Notably, a reduction from a high to low category of CTCs correlated with objective tumor response. The findings suggest CTCs may have prognostic value for patients with mCRPC both at baseline and following changes during therapy, Dr. de Bono and his colleagues concluded. They are also carrying out additional analyses of the associations of CTC androgen receptor variant 7, chromosomal instability, heterogeneity status, single-cell genotypes, and the presence of CTCs with small-cell/neuroendocrine morphology.