EGFR Protein Expression in KRAS Wild-Type Metastatic Colorectal Cancer Is Another Negative Predictive Factor of the Cetuximab Therapy

被引:6
作者
Uhlyarik, Andrea [1 ]
Piurko, Violetta [2 ]
Papai, Zsuzsanna [1 ]
Raso, Erzsebet [2 ]
Lahm, Erika [1 ]
Kiss, Edina [1 ]
Sikter, Marta [1 ]
Vachaja, Jozsef [1 ]
Kenessey, Istvan [2 ]
Timar, Jozsef [2 ]
机构
[1] Hungarian Def Forces, Med Ctr, Dept Oncol, Budapest 1065, Hungary
[2] Semmelweis Univ, Dept Pathol 2, Budapest 1091, Hungary
关键词
metastatic colorectal cancer; Cetuximab; EGFR protein; survival; GROWTH-FACTOR RECEPTOR; PLUS CETUXIMAB; IMMUNOHISTOCHEMISTRY; CHEMOTHERAPY; RESISTANCE; ANTIBODIES; MUTATIONS; LANDSCAPE; BENEFIT;
D O I
10.3390/cancers12030614
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The selection of colorectal cancer patients for anti-epidermal growth factor receptor (EGFR) antibody therapy is based on the determination of their RAS mutation status-a strongly negative predictive factor-since the protein target, EGFR, is not a reliable predictor of therapeutic response. In this study, we revisited the EGFR protein issue using a cohort of 90 patients with KRAS exon2 wild-type colorectal cancer who have been treated with cetuximab therapy. Twenty-nine of these patients had metastatic tissue available for analysis. The level of EGFR protein expression in the patients was determined by immunohistochemistry and evaluated by H-score (HS) methodology. Progression-free survival (PFS) and overall survival (OS) of the patients were determined according to the EGFR-HS ranges of both the primary and metastatic tissues using Kaplan-Meyer statistics. In the case of primary tumors, EGFR scores lower than HS = 200 were associated with significantly longer OS. In the case of metastatic tissues, all levels lower than the EGFR-HS range chosen were associated with significantly longer OS. These results are explained by the fact that metastatic tissues rarely maintained the expression levels of the primary tumors. On the other hand, high EGFR expression levels in either primary tumors or metastatic tissues were associated with multiple metastatic disease. This suggests a negative prognostic role of EGFR expression. However, in a multivariate analysis, one-sidedness remained a strong independent predictive factor of survival. Previous studies demonstrated that the EGFR expression level depends on sidedness. Therefore, a subgroup analysis of the left- and right-sided cases was performed on both primary and metastatic tissues. In the case of metastic tissues, an analysis confirmed a better OS in low EGFR protein-expressing cases than in high EGFR protein-expressing cases. Collectively, these data suggest that EGFR protein expression is another negative predictive factor of the efficacy of cetuximab therapy of KRAS exon2 wild-type colorectal cancer.
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页数:12
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共 26 条
[1]   EGFR gene copy number predicts response to anti-EGFR treatment in RAS wild type and RAS/BRAF/PIK3CA wild type metastatic colorectal cancer [J].
Algars, Annika ;
Sundstrom, Jari ;
Lintunen, Minnamaija ;
Jokilehto, Terhi ;
Kytola, Soili ;
Kaare, Milja ;
Vainionpaa, Reetta ;
Orpana, Arto ;
Osterlund, Pia ;
Ristimaki, Ari ;
Carpen, Olli ;
Ristamaki, Raija .
INTERNATIONAL JOURNAL OF CANCER, 2017, 140 (04) :922-929
[2]  
Annadappa G., 2019, CLIN CANCER RES, V25, P3830
[3]   The genomic landscape of response to EGFR blockade in colorectal cancer [J].
Bertotti, Andrea ;
Papp, Eniko ;
Jones, Sian ;
Adleff, Vilmos ;
Anagnostou, Valsamo ;
Lupo, Barbara ;
Sausen, Mark ;
Phallen, Jillian ;
Hruban, Carolyn A. ;
Tokheim, Collin ;
Niknafs, Noushin ;
Nesselbush, Monica ;
Lytle, Karli ;
Sassi, Francesco ;
Cottino, Francesca ;
Migliardi, Giorgia ;
Zanella, Eugenia R. ;
Ribero, Dario ;
Russolillo, Nadia ;
Mellano, Alfredo ;
Muratore, Andrea ;
Paraluppi, Gianluca ;
Salizzoni, Mauro ;
Marsoni, Silvia ;
Kragh, Michael ;
Lantto, Johan ;
Cassingena, Andrea ;
Li, Qing Kay ;
Karchin, Rachel ;
Scharpf, Robert ;
Sartore-Bianchi, Andrea ;
Siena, Salvatore ;
Diaz, Luis A., Jr. ;
Trusolino, Livio ;
Velculescu, Victor E. .
NATURE, 2015, 526 (7572) :263-+
[4]   FOLFOX4 plus cetuximab treatment and RAS mutations in colorectal cancer [J].
Bokemeyer, C. ;
Koehne, C. -H. ;
Ciardiello, F. ;
Lenz, H. -J. ;
Heinemann, V. ;
Klinkhardt, U. ;
Beier, F. ;
Duecker, K. ;
van Krieken, J. H. ;
Tejpar, S. .
EUROPEAN JOURNAL OF CANCER, 2015, 51 (10) :1243-1252
[5]   Addition of cetuximab to chemotherapy as first-line treatment for KRAS wild-type metastatic colorectal cancer: Pooled analysis of the CRYSTAL and OPUS randomised clinical trials [J].
Bokemeyer, Carsten ;
Van Cutsem, Eric ;
Rougier, Philippe ;
Ciardiello, Fortunato ;
Heeger, Steffen ;
Schlichting, Michael ;
Celik, Ilhan ;
Koehne, Claus-Henning .
EUROPEAN JOURNAL OF CANCER, 2012, 48 (10) :1466-1475
[6]   The impact of primary tumor location on efficacy of cetuximab in metastatic colorectal cancer patients with different Kras status: a systematic review and meta-analysis [J].
Cao, De-Dong ;
Xu, Hui-Lin ;
Xu, Xi-Ming ;
Ge, Wei .
ONCOTARGET, 2017, 8 (32) :53631-53641
[7]   Epidermal Growth Factor Receptor Inconsistency by Immunohistochemistry Method Using Different Monoclonal Antibodies in Colorectal Cancer Patients [J].
Chi-Chen, Fan ;
Tao-Yeuan, Wang ;
Chien-Min, Kung .
CLINICAL LABORATORY, 2015, 61 (11) :1635-1641
[8]   Cetuximab shows activity in colorectal cancer patients with tumors that do not express the epidermal growth factor receptor by immunohistochemistry [J].
Chung, KY ;
Shia, J ;
Kemeny, NE ;
Shah, M ;
Schwartz, GK ;
Tse, A ;
Hamilton, A ;
Pan, D ;
Schrag, D ;
Schwartz, L ;
Klimstra, DS ;
Fridman, D ;
Kelsen, DP ;
Saltz, LB .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (09) :1803-1810
[9]   Subtype-specific KRAS mutations in advanced lung adenocarcinoma: A retrospective study of patients treated with platinum-based chemotherapy [J].
Cserepes, Mihaly ;
Ostoros, Gyula ;
Lohinai, Zoltan ;
Raso, Erzsebet ;
Barbai, Tamas ;
Timar, Jozsef ;
Rozsas, Anita ;
Moldvay, Judit ;
Kovalszky, Ilona ;
Fabian, Katalin ;
Gyulai, Marton ;
Ghanim, Bahil ;
Laszlo, Viktoria ;
Klikovits, Thomas ;
Hoda, Mir Alireza ;
Grusch, Michael ;
Berger, Walter ;
Klepetko, Walter ;
Hegedus, Balazs ;
Dome, Balazs .
EUROPEAN JOURNAL OF CANCER, 2014, 50 (10) :1819-1828
[10]   Protocol modifications influence the result of EGF receptor immunodetection by EGFR pharmDX™ in paraffin-embedded cancer tissues [J].
Derecskei, Katalin ;
Moldvay, Judit ;
Bogos, Krisztina ;
Timar, Jozsef .
PATHOLOGY & ONCOLOGY RESEARCH, 2006, 12 (04) :243-246