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Genetic Variant as a Selection Marker for Anti–Prostate Stem Cell Antigen Immunotherapy of Bladder Cancer
Author(s) -
Indu Kohaar,
Patricia PorterGill,
Petra H. Lenz,
YiPing Fu,
Adam Mumy,
Wei Tang,
Andrea B. Apolo,
Nathaniel Rothman,
Dalsu Baris,
Alan R. Schned,
Kris Ylaya,
Molly Schwenn,
Alison Johnson,
Michael A. Jones,
Masatoshi Kida,
Debra T. Silverman,
Stephen M. Hewitt,
Lee E. Moore,
Ludmila ProkuninaOlsson
Publication year - 2012
Publication title -
jnci journal of the national cancer institute
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.797
H-Index - 356
eISSN - 1460-2105
pISSN - 0027-8874
DOI - 10.1093/jnci/djs458
Subject(s) - bladder cancer , immunotherapy , prostate cancer , medicine , prostate , oncology , antigen , cancer , monoclonal antibody , cancer research , antibody , immunology
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.

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