A monoclonal antibody against
prostate stem cell antigen (PSCA) has emerged as a novel cancer therapy
currently being tested in clinical trials for prostate and pancreatic cancers,
but this treatment is likely to be efficient only in patients with
PSCA-expressing tumors. The present study demonstrates that a genetic variant
(rs2294008) discovered by bladder cancer genome-wide association studies is a
strong predictor of PSCA protein expression in bladder tumors, as measured by
two-sided multivariable linear regression (P = 6.46×10(-11); n = 278). The
association pattern is similar in non-muscle-invasive tumors, stages Ta (P =
3.10×10(-5); n = 173) and T1 (P = 2.64×10(-5); n = 60), and muscle-invasive
tumors, stages T2 (P =.01; n = 23) and T3/4 (P =.03; n = 22). The study
suggests that anti-PSCA immunotherapy might be beneficial for bladder cancer
patients with high tumor PSCA expression, which is statistically significantly
associated with the presence of CT and TT genotypes of a common genetic
variant, rs2294008. Future clinical studies will be needed to validate PSCA as
a therapeutic target for bladder cancer.
Source: Genetic variant as
a selection marker for anti-prostate stem cell antigen immunotherapy of bladder
cancer. Kohaar I, Porter-Gill P, Lenz P, Fu YP, Mumy A, Tang W, Apolo AB,
Rothman N, Baris D, Schned AR, Ylaya K, Schwenn M, Johnson A, Jones M, Kida M,
Silverman DT, Hewitt SM, Moore LE, Prokunina-Olsson L (prokuninal@mail.nih.gov). J Natl
Cancer Inst. 2013 Jan 2;105(1):69-73.
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