Impact of neutrophil-lymphocyte and platelet-lymphocyte ratio on antiEGFR and bevacizumab efficacy in metastatic colorectal cancer

被引:2
作者
Dogan, Ender [1 ]
Bozkurt, Oktay [1 ]
Sakalar, Teoman [1 ]
Derin, Sumeyra [1 ]
Inanc, Mevlude [1 ]
Ozkan, Metin [1 ]
机构
[1] Erciyes Univ, Dept Med Oncol, Med Fac, Kayseri, Turkey
来源
JOURNAL OF BUON | 2019年 / 24卷 / 05期
关键词
inflammation markers; colorectal cancer; antiEGFR; bevacizumab; PRETREATMENT NEUTROPHIL; PREDICTIVE BIOMARKERS; MONOCLONAL-ANTIBODY; SURVIVAL; INFLAMMATION; IMMUNITY;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: The purpose of this study was to determine the influence of the neutrophil-lymphocyte ratio (NLR) and the platelet-lymphocyte ratio (PLR) on antiEGFR and bevacizumab efficacy in metastatic colorectal cancer patients. Methods: All metastatic colorectal cancer patients who had received chemotherapy and biological agents as first-line treatment at Erciyes University Hospital were retrospectively reviewed. NLR and PLR were each divided into two groups, as high and low. The NLR high group was compared with the low group and the PLR high group was compared with the low group in patients in terms of progression-free survival (PFS) and overall survival (OS), separately. Cox regression and the Kaplan Meier method were used. Results: One hundred and thirty (58%) of the patients had received bevacizumab and 94 (42%) had received antiEGFR therapy (cetuximab or panitumumab). In the bevacizumab group, PFS was 9 months in the NLR high group and 11 months in the NLR low group (p=0.013). OS was 23 months in the NLR high group and 27 months in the NLR low group (p=0.734). There was no statistically significant OS difference in patients who had received antiEGFR therapy according to NLR. There was no statistically significant PFS difference in patients who received bevacizumab according to PLR. In the antiEGFR group, PFS was 9 months (95% CI, 8.07-13.55) in the PLR high group and 18 months (95% CI, 12.02-18.68) in the PLR low group, with statistically significant difference (p=0.040). There was no statistically significant OS difference in patients who had received antiEGFR therapy according to PLR. Conclusions: NLR and PLR are important inflammatory markers. In patients who had received bevacizumab, PFS was longer in the NLR low group than in the high group. In patients who had received antiEGFR, PFS was longer in the PLR low group than in the high group.
引用
收藏
页码:1861 / 1869
页数:9
相关论文
共 30 条
[1]   Serum proinflammatory cytokines and its relationship to clinical parameters in lung cancer patients with reactive thrombocytosis [J].
Alexandrakis, MG ;
Passam, FH ;
Perisinakis, K ;
Ganotakis, E ;
Margantinis, G ;
Kyriakou, DS ;
Bouros, D .
RESPIRATORY MEDICINE, 2002, 96 (08) :553-558
[2]   Activated platelets rescue apoptotic cells via paracrine activation of EGFR and DNA-dependent protein kinase [J].
Au, A. E-L ;
Sashindranath, M. ;
Borg, R. J. ;
Kleifeld, O. ;
Andrews, R. K. ;
Gardiner, E. E. ;
Medcalf, R. L. ;
Samson, A. L. .
CELL DEATH & DISEASE, 2014, 5 :e1410-e1410
[3]   Mechanisms of resistance to antiangiogenesis therapy [J].
Azam, Faisal ;
Mehta, Shaveta ;
Harris, Adrian L. .
EUROPEAN JOURNAL OF CANCER, 2010, 46 (08) :1323-1332
[4]   Preoperative platelet-lymphocyte ratio is an independent factor of poor prognosis after curative surgery for colon cancer [J].
Bailon-Cuadrado, Martin ;
Choolani-Bhojwani, Ekta ;
Tejero-Pintor, Francisco J. ;
Sanchez-Gonzalez, Javier ;
Rodriguez-Lopez, Mario ;
Perez-Saborido, Baltasar ;
Marcos-Rodriguez, Jose L. .
UPDATES IN SURGERY, 2018, 70 (01) :33-39
[5]   Systemic inflammatory status at baseline predicts bevacizumab benefit in advanced non-small cell lung cancer patients [J].
Botta, Cirino ;
Barbieri, Vito ;
Ciliberto, Domenico ;
Rossi, Antonio ;
Rocco, Danilo ;
Addeo, Raffaele ;
Staropoli, Nicoletta ;
Pastina, Pierpaolo ;
Marvaso, Giulia ;
Martellucci, Ignazio ;
Guglielmo, Annamaria ;
Pirtoli, Luigi ;
Sperlongano, Pasquale ;
Gridelli, Cesare ;
Caraglia, Michele ;
Tassone, Pierfrancesco ;
Tagliaferri, Pierosandro ;
Correale, Pierpaolo .
CANCER BIOLOGY & THERAPY, 2013, 14 (06) :469-475
[6]  
Bozkurt O, 2015, J BUON, V20, P1432
[7]   Platelets, NETs and cancer [J].
Cedervall, Jessica ;
Hamidi, Anahita ;
Olsson, Anna-Karin .
THROMBOSIS RESEARCH, 2018, 164 :S148-S152
[8]   Cetuximab monotherapy and cetuximab plus irinotecan in irinotecan-refractory metastatic colorectal cancer [J].
Cunningham, D ;
Humblet, Y ;
Siena, S ;
Khayat, D ;
Bleiberg, H ;
Santoro, A ;
Bets, D ;
Mueser, M ;
Harstrick, A ;
Verslype, C ;
Chau, I ;
Van Cutsem, E .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 351 (04) :337-345
[9]   Immunity, Inflammation, and Cancer [J].
Grivennikov, Sergei I. ;
Greten, Florian R. ;
Karin, Michael .
CELL, 2010, 140 (06) :883-899
[10]   The association of pre-treatment neutrophil to lymphocyte ratio with response rate, progression free survival, and overall survival of patients treated with sunitinib for metastatic renal cell carcinoma [J].
Keizman, Daniel ;
Ish-Shalom, Maya ;
Huang, Peng ;
Eisenberger, Mario A. ;
Pili, Roberto ;
Hammers, Hans ;
Carducci, Michael A. .
EUROPEAN JOURNAL OF CANCER, 2012, 48 (02) :202-208