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pERK, pAKT and p53 as tissue biomarkers in erlotinib-treated patients with advanced pancreatic cancer: a translational subgroup analysis from AIO-PK0104

Authors :
Ormanns, Steffen
Siveke, Jens
Heinemann, Volker
Haas, Michael L.
Sipos, Bence
Schlitter, Anna Melissa Elissa
Esposito, Iréne
Jung, Andreas
Laubender, Rüdiger Paul Aul
Kruger, Stephan
Vehling-Kaiser, Ursula
Winkelmann, Cornelia
Fischer von Weikersthal, Ludwig
Clemens, Michael Roland
Gauler, Thomas
Märten, Angela
Geissler, Michael
Greten, Tim F.
Kirchner, Thomas
Boeck, Stefan
Source :
BMC Cancer
Publisher :
Springer Nature

Abstract

Background The role of pERK, pAKT and p53 as biomarkers in patients with advanced pancreatic cancer has not yet been defined. Methods Within the phase III study AIO-PK0104 281 patients with advanced pancreatic cancer received an erlotinib-based 1st-line regimen. Archival tissue from 153 patients was available for central immunohistochemistry staining for pERK, pAKT and p53. Within a subgroup analysis, biomarker data were correlated with efficacy endpoints and skin rash using a Cox regression model. Results Fifty-five out of 153 patients were classified as pERKlow and 98 patients as pERKhigh; median overall survival (OS) was 6.2 months and 5.7 months, respectively (HR 1.29, p = 0.16). When analysing pERK as continuous variable, the pERK score was significantly associated with OS (HR 1.06, 95% CI 1.0-1.12, p = 0.05). Twenty-one of 35 patients were pAKTlow and 14/35 pAKThigh with a corresponding median OS of 6.4 months and 6.8 months, respectively (HR 1.03, p = 0.93). Four out of 50 patients had a complete loss of p53 expression, 20 patients a regular expression and 26 patients had tumors with p53 overexpression. The p53 status had no impact on OS (p = 0.91); however, a significant improvement in progression-free survival (PFS) (6.0 vs 1.8 months, HR 0.24, p = 0.02) and a higher rate of skin rash (84% vs 25%, p = 0.02) was observed for patients with a regular p53 expression compared to patients with a complete loss of p53. Conclusion pERK expression may have an impact on OS in erlotinib-treated patients with advanced pancreatic cancer; p53 should be further investigated for its potential role as a predictive marker for PFS and skin rash. Trial registration NCT00440167 (registration date: February 22, 2007). Electronic supplementary material The online version of this article (doi:10.1186/1471-2407-14-624) contains supplementary material, which is available to authorized users.

Details

Language :
English
ISSN :
14712407 and 00440167
Volume :
14
Issue :
1
Database :
OpenAIRE
Journal :
BMC Cancer
Accession number :
edsair.pmid.dedup....e4012c00acd2e219498c925ef594cde7
Full Text :
https://doi.org/10.1186/1471-2407-14-624