p53-autoantibody may be more sensitive than CA-125 in monitoring microscopic and macroscopic residual disease after primary therapy for epithelial ovarian cancer

J Cancer Res Clin Oncol. 2013 Jul;139(7):1207-10. doi: 10.1007/s00432-013-1432-2. Epub 2013 Apr 11.

Abstract

Purpose: To evaluate the use of p53-autoantibodies (p53-aab) for monitoring minimal disease after standard therapy of advanced epithelial ovarian cancer (EOC).

Methods: Retrospective analysis of p53-aab in preoperative and long-term follow-up serum samples from 10 patients selected for representing three relevant EOC subgroups: platinum-sensitive disease after macroscopic complete debulking (n = 4) and platinum-sensitive (n = 3) or platinum-resistant disease (n = 3), both after suboptimal debulking with residual tumor of <1 cm diameter. p53-aab levels were quantified by a sandwich ELISA in two independent experiments. CA-125 values of all samples and clinical information were retrieved from medical records.

Results: Patients with early relapse (median PFS 7 months, n = 8) had high p53-aab levels throughout follow-up while CA-125 values had dropped below the cut-off after primary surgery during or after chemotherapy in these cases. Patients with seroconversion to p53-aab negativity experienced prolonged PFS (n = 2; #1: 50 months, #2: no evidence of disease for 36 months until last follow-up). Continued p53-aab positivity was not related to the resection status or platinum sensitivity.

Conclusions: p53-autoantibodies may be a highly sensitive marker for minimal residual tumor mass after surgery and/or chemotherapy rather than standard CA-125, possibly due to the different nature of these markers. CA-125 released by cancer cells is related to tumor mass, whereas p53-aab levels can indicate the presence of few tumor cells due to amplification by the immune system. Seroconversion of p53-aab could be associated with long-term survival.

MeSH terms

  • Autoantibodies / blood*
  • Biomarkers, Tumor / blood*
  • CA-125 Antigen / blood*
  • Carcinoma, Ovarian Epithelial
  • Combined Modality Therapy
  • Female
  • Humans
  • Neoplasm, Residual
  • Neoplasms, Glandular and Epithelial / blood*
  • Neoplasms, Glandular and Epithelial / immunology
  • Neoplasms, Glandular and Epithelial / therapy
  • Ovarian Neoplasms / blood*
  • Ovarian Neoplasms / immunology
  • Ovarian Neoplasms / therapy
  • Retrospective Studies
  • Tumor Suppressor Protein p53 / immunology*

Substances

  • Autoantibodies
  • Biomarkers, Tumor
  • CA-125 Antigen
  • TP53 protein, human
  • Tumor Suppressor Protein p53