ASSESSMENT OF THE BIOLOGIC MARKERS P53, KI-67, AND APOPTOTIC INDEX ASPREDICTIVE INDICATORS OF PROSTATE CARCINOMA RECURRENCE AFTER SURGERY

Citation
Amf. Stapleton et al., ASSESSMENT OF THE BIOLOGIC MARKERS P53, KI-67, AND APOPTOTIC INDEX ASPREDICTIVE INDICATORS OF PROSTATE CARCINOMA RECURRENCE AFTER SURGERY, Cancer, 82(1), 1998, pp. 168-175
Citations number
59
Categorie Soggetti
Oncology
Journal title
CancerACNP
ISSN journal
0008543X
Volume
82
Issue
1
Year of publication
1998
Pages
168 - 175
Database
ISI
SICI code
0008-543X(1998)82:1<168:AOTBMP>2.0.ZU;2-V
Abstract
BACKGROUND. This study was designed to evaluate the potential of the m olecular and cellular markers p53, Ki-67, and apoptotic index (AI) as adjuncts to the commonly available variables of tumor grade, clinical stage, and serum prostate specific antigen to predict prostate carcino ma recurrence after radical prostatectomy. METHODS. Representative pun ch biopsy specimens of prostate carcinoma from whole mount paraffin bl ocks were evaluated from 47 men who underwent radical prostatectomy. T wo groups were defined: those without evidence of prostate carcinoma r ecurrence after 5 years of follow-up (N = 30) and those with carcinoma recurrence (N = 17). Gleason grade, clustered p53 immunostaining, Ki- 67 immunostaining, and AI were determined by standard techniques. RESU LTS. All variables tested were associated with disease recurrence by u nivariate analysis: AI (P = 0.005), clustered p53 immunostaining (P = 0.0070), and Ki-67 immunostaining (P = 0.0390). Using multivariate ana lyses that included each biomarker with routinely available features, only AI (P = 0.0234) and clustered p53 immunostaining (P = 0.0389) add ed independent prognostic information (Ki-67 immunostaining, P = 0.128 5). In the final logistic regression model that included standard vari ables with AI and p53, only AI reached statistical significance (P = 0 .0332). CONCLUSIONS. The continued assessment of additional biomarkers for prostate carcinoma recurrence is important to identify better tho se patients who may be candidates for early adjuvant therapy and also to further our understanding of the neoplastic potential of a particul ar malignancy. (C) 1998 American Cancer Society.