High serum level of C-reactive protein is associated with worse outcome of patients with advanced-stage NSCLC treated with erlotinib
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
26088452
DOI
10.1007/s13277-015-3660-3
PII: 10.1007/s13277-015-3660-3
Knihovny.cz E-zdroje
- Klíčová slova
- Biomarker, C-reactive protein, EGFR-TKI, Erlotinib, Lung cancer, NSCLC, Prediction,
- MeSH
- C-reaktivní protein genetika metabolismus MeSH
- dospělí MeSH
- erbB receptory antagonisté a inhibitory MeSH
- erlotinib aplikace a dávkování MeSH
- inhibitory proteinkinas aplikace a dávkování MeSH
- lidé středního věku MeSH
- lidé MeSH
- mutace MeSH
- nádorové biomarkery krev genetika MeSH
- nemalobuněčný karcinom plic krev genetika patologie MeSH
- přežití bez známek nemoci MeSH
- senioři MeSH
- staging nádorů MeSH
- výsledek terapie MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- C-reaktivní protein MeSH
- EGFR protein, human MeSH Prohlížeč
- erbB receptory MeSH
- erlotinib MeSH
- inhibitory proteinkinas MeSH
- nádorové biomarkery MeSH
Erlotinib is a low molecular weight tyrosine kinase inhibitor (TKI) directed at epidermal growth factor receptor (EGFR), widely used in the treatment of locally advanced or metastatic-stage non-small cell lung cancer (NSCLC). Although introduction of EGFR-TKIs have significantly extended survival of advanced-stage NSCLC patients, their efficacy in the entire patient population is relatively low. Aside from activating EGFR mutations, no reliable biochemical or molecular predictors of response to erlotinib have been established. The aim of our retrospective study was to evaluate the association of baseline serum levels of C-reactive protein (CRP) with outcomes in patients with advanced-stage NSCLC treated with erlotinib. We retrospectively analyzed clinical data of 595 patients with advanced-stage NSCLC (IIIB or IV) treated with erlotinib. Serum CRP was measured using an immunoturbidimetric method. High baseline levels of CRP (≥10 mg/l) were measured in 387 (65 %) patients, and normal levels (<10 mg/l) were measured in 208 (35 %) patients. The median progression-free survival (PFS) and overall survival (OS) for patients with high CRP was 1.8 and 7.7 compared to 2.8 and 14.4 months for patients with low CRP (p < 0.001 and p < 0.001). The multivariable Cox proportional hazards model revealed that CRP was significantly associated with PFS and also with OS (hazard ratio (HR) = 1.57, p < 0.001, and HR = 1.63, p < 0.001, respectively). In conclusion, the results of the conducted retrospective study suggest that high baseline level of CRP was independently associated with worse outcome of patients with advanced-stage NSCLC treated with erlotinib. CRP is a commonly used biomarker which is simple and easy to detect, and thus, it is feasible for the use in the routine clinical practice.
Biomedical Center Faculty of Medicine in Pilsen Charles University Prague Pilsen Czech Republic
Center for Applied Genomics of Solid Tumours Genomac Research Institute Prague Czech Republic
Institute of Biostatistics and Analysis Faculty of Medicine Masaryk University Brno Czech Republic
Zobrazit více v PubMed
Ann Surg. 2003 Aug;238(2):197-202 PubMed
Cancer. 2007 Sep 15;110(6):1241-7 PubMed
J Natl Cancer Inst. 2000 Feb 2;92 (3):205-16 PubMed
Eur J Surg Oncol. 2009 Jun;35(6):605-10 PubMed
Mol Immunol. 2001 Aug;38(2-3):189-97 PubMed
J Clin Oncol. 2006 Nov 1;24(31):5034-42 PubMed
Hepatology. 1993 Nov;18(5):1216-23 PubMed
Mol Cancer Ther. 2012 Oct;11(10 ):2254-64 PubMed
Onkologie. 2008 Dec;31(12 ):665-70 PubMed
Ann N Y Acad Sci. 2009 Aug;1171:59-76 PubMed
J Biol Regul Homeost Agents. 1987 Oct-Dec;1(4):173-6 PubMed
Lancet Oncol. 2012 Mar;13(3):239-46 PubMed
Eur Respir J. 2001 Dec;18(6):1059-68 PubMed
Oncology. 2010;79(5-6):355-62 PubMed
Br J Cancer. 2002 Jul 29;87(3):264-7 PubMed
Br J Cancer. 2004 Dec 13;91(12):1993-5 PubMed
Eur J Cancer. 2010 Mar;46(4):765-81 PubMed
J Surg Oncol. 2008 Dec 1;98(7):540-4 PubMed
Biochem J. 1997 Oct 15;327 ( Pt 2):425-9 PubMed
Clin Cancer Res. 2008 Feb 1;14(3):710-4 PubMed
Anticancer Res. 2011 Sep;31(9):2949-55 PubMed
Science. 2004 Jun 4;304(5676):1497-500 PubMed
J Thorac Oncol. 2009 Mar;4(3):326-32 PubMed
N Engl J Med. 2004 May 20;350(21):2129-39 PubMed
Cell. 1999 Aug 6;98(3):295-303 PubMed
Clin Cancer Res. 2005 Dec 1;11(23):8288-94 PubMed
J Clin Oncol. 2008 Sep 10;26(26):4268-75 PubMed
Lancet Oncol. 2012 Mar;13(3):300-8 PubMed
Lancet. 2001 Feb 17;357(9255):539-45 PubMed
Lancet Oncol. 2011 Aug;12(8):735-42 PubMed
N Engl J Med. 2005 Jul 14;353(2):123-32 PubMed
J Exp Med. 1986 Jul 1;164(1):321-6 PubMed
Anticancer Res. 2012 Feb;32(2):491-6 PubMed
CA Cancer J Clin. 2011 Mar-Apr;61(2):69-90 PubMed
Anticancer Res. 2007 Jul-Aug;27(4C):3001-4 PubMed
Nature. 2008 Jul 24;454(7203):436-44 PubMed
N Engl J Med. 1999 Feb 11;340(6):448-54 PubMed