Potential value of PTEN in predicting cetuximab response in colorectal cancer: An exploratory study

<p>Abstract</p> <p>Background</p> <p>The epidermal growth factor receptor (EGFR) is over-expressed in 70–75% of colorectal adenocarcinomas (CRC). The anti-EGFR monoclonal antibody cetuximab has been approved for the treatment of metastatic CRC, however tumor response to...

Full description

Bibliographic Details
Main Authors: Koukouma Alona, Gikonti Ioanna, Galanidi Eleni, Bai Maria, Bobos Mattheos, Xanthakis Ioannis, Samantas Epaminontas, Kostopoulos Ioannis, Papamichael Dimitrios, Skarlos Dimosthenis V, Vrettou Eleni, Briasoulis Evangelos, Razis Evangelia, Kafiri Georgia, Papakostas Pavlos, Kalogeras Konstantine T, Kosmidis Paris, Fountzilas George
Format: Article
Language:English
Published: BMC 2008-08-01
Series:BMC Cancer
Online Access:http://www.biomedcentral.com/1471-2407/8/234
id doaj-abdf52741a9d408d9f530cea69c7c3c6
record_format Article
spelling doaj-abdf52741a9d408d9f530cea69c7c3c62020-11-24T23:01:48ZengBMCBMC Cancer1471-24072008-08-018123410.1186/1471-2407-8-234Potential value of PTEN in predicting cetuximab response in colorectal cancer: An exploratory studyKoukouma AlonaGikonti IoannaGalanidi EleniBai MariaBobos MattheosXanthakis IoannisSamantas EpaminontasKostopoulos IoannisPapamichael DimitriosSkarlos Dimosthenis VVrettou EleniBriasoulis EvangelosRazis EvangeliaKafiri GeorgiaPapakostas PavlosKalogeras Konstantine TKosmidis ParisFountzilas George<p>Abstract</p> <p>Background</p> <p>The epidermal growth factor receptor (EGFR) is over-expressed in 70–75% of colorectal adenocarcinomas (CRC). The anti-EGFR monoclonal antibody cetuximab has been approved for the treatment of metastatic CRC, however tumor response to cetuximab has not been found to be associated with EGFR over-expression by immunohistochemistry (IHC). The aim of this study was to explore EGFR and the downstream effector phosphatase and tensin homologue deleted on chromosome 10 (PTEN) as potential predictors of response to cetuximab.</p> <p>Methods</p> <p>CRC patients treated with cetuximab by the Hellenic Cooperative Oncology group, whose formalin-fixed paraffin-embedded tumor tissue was available, were included. Tissue was tested for EGFR and PTEN by IHC and fluorescence in situ hybridization (FISH).</p> <p>Results</p> <p>Eighty-eight patients were identified and 72 were included based on the availability of tissue blocks with adequate material for analysis on them. All patients, except one, received cetuximab in combination with chemotherapy. Median follow-up was 53 months from diagnosis and 17 months from cetuximab initiation. At the time of the analysis 53% of the patients had died. Best response was complete response in one and partial response in 23 patients. In 16 patients disease stabilized. Lack of PTEN gene amplification was associated with more responses to cetuximab and longer time to progression (p = 0.042).</p> <p>Conclusion</p> <p>PTEN could be one of the molecular determinants of cetuximab response. Due to the heterogeneity of the population and the retrospective nature of the study, our results are hypothesis generating and should be approached with caution. Further prospective studies are needed to validate this finding.</p> http://www.biomedcentral.com/1471-2407/8/234
collection DOAJ
language English
format Article
sources DOAJ
author Koukouma Alona
Gikonti Ioanna
Galanidi Eleni
Bai Maria
Bobos Mattheos
Xanthakis Ioannis
Samantas Epaminontas
Kostopoulos Ioannis
Papamichael Dimitrios
Skarlos Dimosthenis V
Vrettou Eleni
Briasoulis Evangelos
Razis Evangelia
Kafiri Georgia
Papakostas Pavlos
Kalogeras Konstantine T
Kosmidis Paris
Fountzilas George
spellingShingle Koukouma Alona
Gikonti Ioanna
Galanidi Eleni
Bai Maria
Bobos Mattheos
Xanthakis Ioannis
Samantas Epaminontas
Kostopoulos Ioannis
Papamichael Dimitrios
Skarlos Dimosthenis V
Vrettou Eleni
Briasoulis Evangelos
Razis Evangelia
Kafiri Georgia
Papakostas Pavlos
Kalogeras Konstantine T
Kosmidis Paris
Fountzilas George
Potential value of PTEN in predicting cetuximab response in colorectal cancer: An exploratory study
BMC Cancer
author_facet Koukouma Alona
Gikonti Ioanna
Galanidi Eleni
Bai Maria
Bobos Mattheos
Xanthakis Ioannis
Samantas Epaminontas
Kostopoulos Ioannis
Papamichael Dimitrios
Skarlos Dimosthenis V
Vrettou Eleni
Briasoulis Evangelos
Razis Evangelia
Kafiri Georgia
Papakostas Pavlos
Kalogeras Konstantine T
Kosmidis Paris
Fountzilas George
author_sort Koukouma Alona
title Potential value of PTEN in predicting cetuximab response in colorectal cancer: An exploratory study
title_short Potential value of PTEN in predicting cetuximab response in colorectal cancer: An exploratory study
title_full Potential value of PTEN in predicting cetuximab response in colorectal cancer: An exploratory study
title_fullStr Potential value of PTEN in predicting cetuximab response in colorectal cancer: An exploratory study
title_full_unstemmed Potential value of PTEN in predicting cetuximab response in colorectal cancer: An exploratory study
title_sort potential value of pten in predicting cetuximab response in colorectal cancer: an exploratory study
publisher BMC
series BMC Cancer
issn 1471-2407
publishDate 2008-08-01
description <p>Abstract</p> <p>Background</p> <p>The epidermal growth factor receptor (EGFR) is over-expressed in 70–75% of colorectal adenocarcinomas (CRC). The anti-EGFR monoclonal antibody cetuximab has been approved for the treatment of metastatic CRC, however tumor response to cetuximab has not been found to be associated with EGFR over-expression by immunohistochemistry (IHC). The aim of this study was to explore EGFR and the downstream effector phosphatase and tensin homologue deleted on chromosome 10 (PTEN) as potential predictors of response to cetuximab.</p> <p>Methods</p> <p>CRC patients treated with cetuximab by the Hellenic Cooperative Oncology group, whose formalin-fixed paraffin-embedded tumor tissue was available, were included. Tissue was tested for EGFR and PTEN by IHC and fluorescence in situ hybridization (FISH).</p> <p>Results</p> <p>Eighty-eight patients were identified and 72 were included based on the availability of tissue blocks with adequate material for analysis on them. All patients, except one, received cetuximab in combination with chemotherapy. Median follow-up was 53 months from diagnosis and 17 months from cetuximab initiation. At the time of the analysis 53% of the patients had died. Best response was complete response in one and partial response in 23 patients. In 16 patients disease stabilized. Lack of PTEN gene amplification was associated with more responses to cetuximab and longer time to progression (p = 0.042).</p> <p>Conclusion</p> <p>PTEN could be one of the molecular determinants of cetuximab response. Due to the heterogeneity of the population and the retrospective nature of the study, our results are hypothesis generating and should be approached with caution. Further prospective studies are needed to validate this finding.</p>
url http://www.biomedcentral.com/1471-2407/8/234
work_keys_str_mv AT koukoumaalona potentialvalueofpteninpredictingcetuximabresponseincolorectalcanceranexploratorystudy
AT gikontiioanna potentialvalueofpteninpredictingcetuximabresponseincolorectalcanceranexploratorystudy
AT galanidieleni potentialvalueofpteninpredictingcetuximabresponseincolorectalcanceranexploratorystudy
AT baimaria potentialvalueofpteninpredictingcetuximabresponseincolorectalcanceranexploratorystudy
AT bobosmattheos potentialvalueofpteninpredictingcetuximabresponseincolorectalcanceranexploratorystudy
AT xanthakisioannis potentialvalueofpteninpredictingcetuximabresponseincolorectalcanceranexploratorystudy
AT samantasepaminontas potentialvalueofpteninpredictingcetuximabresponseincolorectalcanceranexploratorystudy
AT kostopoulosioannis potentialvalueofpteninpredictingcetuximabresponseincolorectalcanceranexploratorystudy
AT papamichaeldimitrios potentialvalueofpteninpredictingcetuximabresponseincolorectalcanceranexploratorystudy
AT skarlosdimosthenisv potentialvalueofpteninpredictingcetuximabresponseincolorectalcanceranexploratorystudy
AT vrettoueleni potentialvalueofpteninpredictingcetuximabresponseincolorectalcanceranexploratorystudy
AT briasoulisevangelos potentialvalueofpteninpredictingcetuximabresponseincolorectalcanceranexploratorystudy
AT razisevangelia potentialvalueofpteninpredictingcetuximabresponseincolorectalcanceranexploratorystudy
AT kafirigeorgia potentialvalueofpteninpredictingcetuximabresponseincolorectalcanceranexploratorystudy
AT papakostaspavlos potentialvalueofpteninpredictingcetuximabresponseincolorectalcanceranexploratorystudy
AT kalogeraskonstantinet potentialvalueofpteninpredictingcetuximabresponseincolorectalcanceranexploratorystudy
AT kosmidisparis potentialvalueofpteninpredictingcetuximabresponseincolorectalcanceranexploratorystudy
AT fountzilasgeorge potentialvalueofpteninpredictingcetuximabresponseincolorectalcanceranexploratorystudy
_version_ 1725638741433778176