TY - JOUR
T1 - Prognostic and predictive value of CEA and CYFRA 21-1 levels in advanced non-small cell lung cancer patients treated with geftinib or erlotinib
AU - Jung, Minkyu
AU - Kim, Se Hyun
AU - Lee, Young Joo
AU - Hong, Soojung
AU - Kang, Young Ae
AU - Kim, Se Kyu
AU - Chang, Joon
AU - Rha, Sun Young
AU - Kim, Joo Hang
AU - Kim, Dae Joon
AU - Cho, Byoung Chul
PY - 2011/7
Y1 - 2011/7
N2 - The prognostic and predictive value of pre-treatment serum levels of carcinoembryonic antigen (CEA) and cyto-keratin-19 fragments (CYFRA 21-1) were assessed in advanced non-small cell lung cancer (NSCLC) patients treated with geftinib or erlotinib. Pre-treatment CEA and CYFRA 21-1 levels were measured in 123 advanced NSCLC patients receiving geftinib or erlotinib. High CEA levels (h-CEA) were significantly associated with females, patients with adenocarcinoma and non-smokers. Low CYFRA 21-1 levels (l-CYFRA 21-1) were significantly associated with a good performance status (ECOG PS 0-1). The overall response rate (RR) was 27.6%, and a higher RR was associated with adenocarcinoma, h-CEA, and epidermal growth factor receptor (EGFR) mutation. Patients with h-CEA had significantly longer progression-free survival (PFS) (P=0.021). Patients with l-CYFRA 21-1 had significantly longer PFS and overall survival (OS) (P=0.006 and P<0.001, respectively). Notably, h-CEA and l-CYFRA 21-1 levels were associated with good prognosis in patients with unknown EGFR mutation status or patients with squamous cell carcinoma (P=0.021 and P=015, respectively). A good ECOG PS (HR=0.45, P=0.017), h-CEA (HR= 0.41, P= 0. 0 07), l-CY F RA 21-1 (H R= 0.52, P=0.025), and an EGFR mutation (HR=0.22, P<0.001) were independently predictive of a longer PFS. A good ECOG PS (H R= 0. 52, P= 0. 018), l- CY FRA 21-1 (HR= 0.36, P= 0.004), and EGFR mutation (HR=0.53, P=0.051) were independently predictive of longer OS. h-CEA and l-CYFRA 21-1 may be prognostic and predictive serum markers for higher response and longer survival in patients with advanced NSCLC receiving geftinib or erlotinib, particularly in patients with unknown EGFR mutation status or patients with squamous cell carcinoma.
AB - The prognostic and predictive value of pre-treatment serum levels of carcinoembryonic antigen (CEA) and cyto-keratin-19 fragments (CYFRA 21-1) were assessed in advanced non-small cell lung cancer (NSCLC) patients treated with geftinib or erlotinib. Pre-treatment CEA and CYFRA 21-1 levels were measured in 123 advanced NSCLC patients receiving geftinib or erlotinib. High CEA levels (h-CEA) were significantly associated with females, patients with adenocarcinoma and non-smokers. Low CYFRA 21-1 levels (l-CYFRA 21-1) were significantly associated with a good performance status (ECOG PS 0-1). The overall response rate (RR) was 27.6%, and a higher RR was associated with adenocarcinoma, h-CEA, and epidermal growth factor receptor (EGFR) mutation. Patients with h-CEA had significantly longer progression-free survival (PFS) (P=0.021). Patients with l-CYFRA 21-1 had significantly longer PFS and overall survival (OS) (P=0.006 and P<0.001, respectively). Notably, h-CEA and l-CYFRA 21-1 levels were associated with good prognosis in patients with unknown EGFR mutation status or patients with squamous cell carcinoma (P=0.021 and P=015, respectively). A good ECOG PS (HR=0.45, P=0.017), h-CEA (HR= 0.41, P= 0. 0 07), l-CY F RA 21-1 (H R= 0.52, P=0.025), and an EGFR mutation (HR=0.22, P<0.001) were independently predictive of a longer PFS. A good ECOG PS (H R= 0. 52, P= 0. 018), l- CY FRA 21-1 (HR= 0.36, P= 0.004), and EGFR mutation (HR=0.53, P=0.051) were independently predictive of longer OS. h-CEA and l-CYFRA 21-1 may be prognostic and predictive serum markers for higher response and longer survival in patients with advanced NSCLC receiving geftinib or erlotinib, particularly in patients with unknown EGFR mutation status or patients with squamous cell carcinoma.
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U2 - 10.3892/etm.2011.273
DO - 10.3892/etm.2011.273
M3 - Article
AN - SCOPUS:79958038844
SN - 1792-0981
VL - 2
SP - 685
EP - 693
JO - Experimental and Therapeutic Medicine
JF - Experimental and Therapeutic Medicine
IS - 4
ER -