Autoimmunity against p53 predicts invasive cancer with poor survival in patients with an ovarian mass

Citation
Fd. Vogl et al., Autoimmunity against p53 predicts invasive cancer with poor survival in patients with an ovarian mass, BR J CANC, 83(10), 2000, pp. 1338-1343
Citations number
33
Categorie Soggetti
Oncology,"Onconogenesis & Cancer Research
Journal title
BRITISH JOURNAL OF CANCER
ISSN journal
00070920 → ACNP
Volume
83
Issue
10
Year of publication
2000
Pages
1338 - 1343
Database
ISI
SICI code
0007-0920(200011)83:10<1338:AAPPIC>2.0.ZU;2-Z
Abstract
Serum autoantibodies against the p53 protein (p53 AAb) were analysed with a newly developed enzyme-linked immunosorbent assay (ELISA) based on highly purified and renatured p53. In a hospital-based cohort study, preoperative sera from 113 patients with ovarian cancer, 15 patients with borderline tum ours and 117 patients with benign tumours of the ovaries were studied. The prevalence of p53 AAb in patients with invasive cancer was 19% (21/113). No p53 AAb were found in patients with borderline lesions or benign tumours. The ELISA had a specificity for malignancy of 99% (1 of 117; false-positive from a patient with severe diabetes mellitus) and a likelihood ratio (LR+) for a positive test result of 21.7 (elevated CA125 and malignancy: LR+ 3.7 ). p53 AAb were only detectable in patients with immunohistochemical staini ng of nuclear p53 in the tumour (P = 0.006). Presence of p53 AAb positively correlated with tumour stage (P = 0.034) and grade (P = 0.009). Kaplan-Mei er analysis showed both a shortened overall survival (P = 0.0016, log-rank) and relapse-free survival (P = 0.055) for p53 AAb-positive patients (media n follow-up 22 months). High titres related to even worse prognosis, p53 AA b independently related to poor survival adjusting for stage (P = 0.026), g rade (P = 0.029) and residual disease after surgery (P = 0.005), Preoperati ve findings of adnexal mass with serum p53 AAb are strongly suggestive of a n aggressive invasive ovarian cancer. (C) 2000 Cancer Research Campaign.