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Published in: International Journal of Clinical Oncology 2/2015

01-04-2015 | Original Article

Low PTEN expression is associated with worse overall survival in head and neck squamous cell carcinoma patients treated with chemotherapy and cetuximab

Authors: Alexandre A. B. A. da Costa, Felipe D’Almeida Costa, Adriana R. Ribeiro, Andréia P. Guimarães, Ludmila T. Chinen, Clóvis A. P. Lopes, Vladmir C. C. de Lima

Published in: International Journal of Clinical Oncology | Issue 2/2015

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Abstract

Background

Platinum-based chemotherapy associated with cetuximab is the first-line treatment for inoperable recurrence or metastatic head and neck squamous cell carcinoma (HNSCC). There is no established biomarker for cetuximab efficacy in HNSCC. The PI3K pathway is one of the most frequently altered pathways in HNSCC. Loss of phosphatase and tensin homolog (PTEN) expression occurs in up to 30 % of cases.

Methods

This was a retrospective analysis of data from 61 patients with inoperable recurrence or metastatic HNSCC treated with cetuximab. PTEN, epidermal growth factor receptor and p16 expression were analyzed by immunohistochemistry and tested for association with clinical outcomes.

Results

Median overall survival was 11.4 months and progression-free survival was 6.9 months. Low PTEN expression was present in 26.2 % of patients and identified patients with worse prognosis. p16 was positive in only 8.5 % of tumors.

Conclusions

Low PTEN expression in patients treated with cetuximab plus chemotherapy emerged as a prognostic biomarker and should be evaluated for its predictive role for cetuximab efficacy.
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Metadata
Title
Low PTEN expression is associated with worse overall survival in head and neck squamous cell carcinoma patients treated with chemotherapy and cetuximab
Authors
Alexandre A. B. A. da Costa
Felipe D’Almeida Costa
Adriana R. Ribeiro
Andréia P. Guimarães
Ludmila T. Chinen
Clóvis A. P. Lopes
Vladmir C. C. de Lima
Publication date
01-04-2015
Publisher
Springer Japan
Published in
International Journal of Clinical Oncology / Issue 2/2015
Print ISSN: 1341-9625
Electronic ISSN: 1437-7772
DOI
https://doi.org/10.1007/s10147-014-0707-1

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