TY - JOUR
T1 - Differential expression of biomarkers in primary non-small cell lung cancer and metastatic sites
AU - Gomez-Roca, Carlos
AU - Raynaud, Christophe M.
AU - Penault-Llorca, Frederique
AU - Mercier, Olaf
AU - Commo, Frederic
AU - Morat, Luc
AU - Sabatier, Laure
AU - Dartevelle, Philipe
AU - Taranchon, Estelle
AU - Besse, Benjamin
AU - Validire, Pierre
AU - Italiano, Antoine
AU - Soria, Jean Charles
N1 - Funding Information:
Supported by DUERCC (Diplome Universitaire Europeen de Recherche Clinique en Cancerologie-Université Paris XI-France) grant (to C.G.-R.) and CEA-Lilly fellowship (to C.R.). The work in the L.S. laboratory was supported by TELINCA. Christophe Raynaud is a doctoral fellow.
PY - 2009/1/1
Y1 - 2009/1/1
N2 - INTRODUCTION: The use of biomarkers to evaluate the presence of a target or to select a specific therapy is increasingly advocated. The correlation of biomarker expression between the primary tumor and its corresponding metastasis has not yet been well documented and analyzed in patients with non-small cell lung cancer (NSCLC). METHODS: The expression of epidermal growth factor receptor (EGFR), excision repair cross-complementing (ERCC1), vascular-endothelial growth factor receptor, and Ki-67 was immunohistochemically analyzed in tumor samples of primary NSCLC and one corresponding metastasis in a population of 49 patients. RESULTS: Sixteen cases (33%) displayed clear discordance in the EGFR status between the primary tumor and the metastasis, with a significant trend toward downregulation of EGFR in the metastasis (p = 0.01). The ERCC1 status was discordant in 20 cases (41%), with a trend toward overexpression in brain and adrenal metastases (p = 0.01 and p = 0.08, respectively). The vascular-endothelial growth factor receptor and Ki-67 statuses were discordant in 13 (27%) and 15 (31%) cases, respectively. No difference in expression was observed between synchronous and metachronous metastasis. CONCLUSION: Biomarker expression is discordant between the primary tumor and its corresponding metastasis in about one third of patients with NSCLC. These findings should be considered in the setting of clinical trials and further explored using frozen material and high-throughput techniques.
AB - INTRODUCTION: The use of biomarkers to evaluate the presence of a target or to select a specific therapy is increasingly advocated. The correlation of biomarker expression between the primary tumor and its corresponding metastasis has not yet been well documented and analyzed in patients with non-small cell lung cancer (NSCLC). METHODS: The expression of epidermal growth factor receptor (EGFR), excision repair cross-complementing (ERCC1), vascular-endothelial growth factor receptor, and Ki-67 was immunohistochemically analyzed in tumor samples of primary NSCLC and one corresponding metastasis in a population of 49 patients. RESULTS: Sixteen cases (33%) displayed clear discordance in the EGFR status between the primary tumor and the metastasis, with a significant trend toward downregulation of EGFR in the metastasis (p = 0.01). The ERCC1 status was discordant in 20 cases (41%), with a trend toward overexpression in brain and adrenal metastases (p = 0.01 and p = 0.08, respectively). The vascular-endothelial growth factor receptor and Ki-67 statuses were discordant in 13 (27%) and 15 (31%) cases, respectively. No difference in expression was observed between synchronous and metachronous metastasis. CONCLUSION: Biomarker expression is discordant between the primary tumor and its corresponding metastasis in about one third of patients with NSCLC. These findings should be considered in the setting of clinical trials and further explored using frozen material and high-throughput techniques.
KW - Biomarker
KW - Corresponding metastasis
KW - ERCC1
KW - Non-small cell lung cancer
KW - Primary tumor
UR - http://www.scopus.com/inward/record.url?scp=70349706155&partnerID=8YFLogxK
U2 - 10.1097/JTO.0b013e3181b44321
DO - 10.1097/JTO.0b013e3181b44321
M3 - Article
AN - SCOPUS:70349706155
SN - 1556-0864
VL - 4
SP - 1212
EP - 1220
JO - Journal of Thoracic Oncology
JF - Journal of Thoracic Oncology
IS - 10
ER -