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PMID: 22056021 Published · ppublish English Clinical Trial, Phase III Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

EGFR expression as a predictor of survival for first-line chemotherapy plus cetuximab in patients with advanced non-small-cell lung cancer: analysis of data from the phase 3 FLEX study.

The Lancet. Oncology ·Vol. 13 ·No. 1 ·2012-01-00 ·Pages 33-42

Pirker R, Pereira JR, von Pawel J, Krzakowski M, Ramlau R, Park K, de Marinis F, Eberhardt WE, Paz-Ares L, Störkel S, Schumacher KM, von Heydebreck A, Celik I, O'Byrne KJ

Abstract

Findings from the phase 3 First-Line ErbituX in lung cancer (FLEX) study showed that the addition of cetuximab to first-line chemotherapy significantly improved overall survival compared with chemotherapy alone (hazard ratio [HR] 0·871, 95% CI 0·762-0·996; p=0·044) in patients with advanced non-small-cell lung cancer (NSCLC). To define patients benefiting most from cetuximab, we studied the association of tumour EGFR expression level with clinical outcome in FLEX study patients. We used prospectively collected tumour EGFR expression data to generate an immunohistochemistry score for FLEX study patients on a continuous scale of 0-300. We used response data to select an outcome-based discriminatory threshold immunohistochemistry score for EGFR expression of 200. Treatment outcome was analysed in patients with low (immunohistochemistry score <200) and high (≥200) tumour EGFR expression. The primary endpoint in the FLEX study was overall survival. We analysed patients from the FLEX intention-to-treat (ITT) population. The FLEX study is registered with ClinicalTrials.gov, number NCT00148798. Tumour EGFR immunohistochemistry data were available for 1121 of 1125 (99·6%) patients from the FLEX study ITT population. High EGFR expression was scored for 345 (31%) evaluable patients and low for 776 (69%) patients. For patients in the high EGFR expression group, overall survival was longer in the chemotherapy plus cetuximab group than in the chemotherapy alone group (median 12·0 months [95% CI 10·2-15·2] vs 9·6 months [7·6-10·6]; HR 0·73, 0·58-0·93; p=0·011), with no meaningful increase in side-effects. We recorded no corresponding survival benefit for patients in the low EGFR expression group (median 9·8 months [8·9-12·2] vs 10·3 months [9·2-11·5]; HR 0·99, 0·84-1·16; p=0·88). A treatment interaction test assessing the difference in the HRs for overall survival between the EGFR expression groups suggested a predictive value for EGFR expression (p=0·044). High EGFR expression is a tumour biomarker that can predict survival benefit from the addition of cetuximab to first-line chemotherapy in patients with advanced NSCLC. Assessment of EGFR expression could offer a personalised treatment approach in this setting. Merck KGaA.

MeSH Terms
Adolescent Adult Aged Aged, 80 and over Antibodies, Monoclonal/administration & dosage Antibodies, Monoclonal, Humanized Antineoplastic Combined Chemotherapy Protocols/adverse effects,therapeutic use Biomarkers, Tumor/antagonists & inhibitors,metabolism Brazil Carcinoma, Non-Small-Cell Lung/drug therapy,enzymology,mortality,pathology Cetuximab Cisplatin/administration & dosage Disease-Free Survival ErbB Receptors/antagonists & inhibitors,metabolism Europe Female Humans Immunohistochemistry Kaplan-Meier Estimate Lung Neoplasms/drug therapy,enzymology,mortality,pathology Male Middle Aged Odds Ratio Patient Selection Proportional Hazards Models Prospective Studies Protein Kinase Inhibitors/administration & dosage Republic of Korea Risk Assessment Risk Factors Survival Rate Time Factors Treatment Outcome Up-Regulation Vinblastine/administration & dosage,analogs & derivatives Vinorelbine Young Adult
Chemicals
Antibodies, Monoclonal Antibodies, Monoclonal, Humanized Biomarkers, Tumor Protein Kinase Inhibitors Vinblastine EGFR protein, human ErbB Receptors Cetuximab Cisplatin Vinorelbine
Authors & Affiliations
14 authors, click to expand affiliations / ORCID
Pirker Robert
Department of Medicine I, Medical University Vienna, Vienna, Austria. [email protected]
Pereira Jose R
von Pawel Joachim
Krzakowski Maciej
Ramlau Rodryg
Park Keunchil
de Marinis Filippo
Eberhardt Wilfried E E
Paz-Ares Luis
Störkel Stephan
Schumacher Karl-Maria
von Heydebreck Anja
Celik Ilhan
O'Byrne Kenneth J
Article Info
Journal
The Lancet. Oncology
Abbr.
Lancet Oncol
ISSN
1474-5488
Published
2012-01-00
Epub
2011-00-04
Pages
33-42
Language
English
Region
England
NLM ID
100957246
Subset
IM
Databases
ClinicalTrials.gov
NCT00148798
Corrections
CommentIn
CommentIn
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