Using an AMACR (P504S)/34βE12/p63 Cocktail for the Detection of Small Focal Prostate Carcinoma in Needle Biopsy Specimens

Zhong Jiang, Cuizhen Li, Andrew Fischer, Karen Dresser, Bruce A. Woda
2005 American Journal of Clinical Pathology  
A b s t r a c t We assessed the usefulness of immunohistochemical analysis with a 3-antibody cocktail (α-methylacyl coenzyme A racemase [AMACR, or P504S], 34βE12, p63) and a double-chromogen reaction for detection of limited prostate cancer in 138 needle biopsy specimens, including 82 with small foci of prostatic adenocarcinoma and 56 benign prostates. When carcinoma was present, red cytoplasmic granular staining (AMACR) in the malignant glands and cells and dark brown nuclear (p63) and
more » ... mic (34βE12) staining in basal cells of adjacent nonmalignant glands were found. Of 82 cases of small foci of prostatic adenocarcinoma, 78 (95%) expressed AMACR; all malignant glands were negative for basal cell staining. All benign glands adjacent to malignant glands were recognized easily by basal cell marker positivity and little or no AMACR expression. No benign glands were simultaneously positive for AMACR and negative for basal cell markers (specificity, 100%). There were no differences in intensity and numbers of positive glands with double-chromogen staining compared with using 1-color staining. Our results indicate that immunohistochemistry with a 3-antibody cocktail and double chromogen is a simple and easy assay that can be used as a routine test, which overcomes the problems of studying small lesions in prostate needle biopsies with multiple immunohistochemical stains. With the major effort in the early detection of prostate cancer by mass screening of men, there have been an increasing number of small foci of cancer encountered on prostate needle biopsy specimens.
doi:10.1309/1g1nk9dbgfnb792l pmid:15842047 fatcat:536txktqvjft5nnjfloxqdgeva