Abstract

BackgroundThe aim of the study was to evaluate predictive and prognostic significance of microtubule-associated protein Tau in epithelial ovarian cancer (EOC) patients treated with paclitaxel and platinum-based chemotherapy.Methods74 patients with EOC (stage I-IV) who underwent cytoreductive surgery followed by standard paclitaxel/platinum chemotherapy were included in the retrospective analysis. Their formalin-fixed, paraffin-embedded tissue specimens were immunohistochemically stained for Tau protein, using semi-quantitative DAKO test. Tau expression was acknowledged as negative (0 and 1+) or positive (2+ and 3+). The correlation between Tau expression, progression free survival (PFS) and overall survival (OS) was evaluated. Statistical analysis included Kaplan-Meyer estimator, long rank test, Mann Whitney test and Cox proportional hazards model.Results25.7% (19/74) and 74.3% (55/74) of the patients were classified as Tau-negative and Tau-positive, respectively. Median PFS was 28.7 months for Tau-negative group and 15.9 months for Tau-positive group (p = 0.0355). In the univariate analysis 3-year OS in Tau-negative and Tau-positive groups was 80.2% and 52.4%, respectively (p = 0.0198). Low expression of protein Tau was associated with better OS, whereas an advanced stage at diagnosis, suboptimal surgery, serous histological type and resistance to first line chemotherapy were each correlated with worse OS (p <0,05). In multivariate analysis only resistance to first line chemotherapy remained significant (HR 22.59; 95% CI, 8.71-58.55; p <0.0001).ConclusionsNegative tau protein seems to be both good prognostic factor and a predictor of response to paclitaxel/platinum-based chemotherapy in EOC patients.

Highlights

  • The aim of the study was to evaluate predictive and prognostic significance of microtubule-associated protein Tau in epithelial ovarian cancer (EOC) patients treated with paclitaxel and platinum-based chemotherapy

  • We have investigated retrospectively the correlation between immunohistochemical expression of protein Tau in the primary tumors and progression free survival (PFS) as well as overall survival (OS) in epithelial ovarian cancer patients treated with debulking surgery followed by standard paclitaxel/platinum chemotherapy

  • Patients We included in our study consecutive patients treated in our site between March 2001 and December 2007, who fulfilled following inclusion criteria: 1) histologically confirmed epithelial ovarian cancer International Federation of Gynaecology and Obstetrics (FIGO) stage IC-IV, 2) history of debulking surgery followed by first-line chemotherapy regimen: paclitaxel (135 mg/m2) with cisplatin (75 mg/m2) or paclitaxel (175 mg/m2) with carboplatin (AUC6), administered every 3 weeks for 6 cycles, 3) accessibility of primary tumor specimens and full medical data

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Summary

Introduction

The aim of the study was to evaluate predictive and prognostic significance of microtubule-associated protein Tau in epithelial ovarian cancer (EOC) patients treated with paclitaxel and platinum-based chemotherapy. Majority of the patients respond to the primary treatment with debulking surgery followed by paclitaxel and platinum-based chemotherapy, many of them experience relapse of the disease within few years after first-line therapy. About one quarter of the patients does not respond to the therapy and those who initially benefit from the treatment incline to experience disease recurrence. There are no molecular agents known to predict the response to the chemotherapy in ovarian cancer as well as patients’ outcome. Revelation of such markers could result in a more effective patient selection to the certain regimens and development of tailored chemotherapy in ovarian cancer

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