Association of EGFR Expression Level and Cetuximab Activity in Patient-Derived Xenograft Models of Human Non-Small Cell Lung Cancer

被引:11
作者
Amendt, Christiane [1 ]
Staub, Eike [1 ]
Friese-Hamim, Manja [1 ]
Stoerkel, Stephan [2 ,3 ]
Stroh, Christopher [1 ]
机构
[1] Merck KGaA, D-64293 Darmstadt, Germany
[2] Univ Witten Herdecke, Inst Pathol, Wuppertal, Germany
[3] HELIOS Hosp Wuppertal, Wuppertal, Germany
关键词
CHEMOTHERAPY PLUS CETUXIMAB; METASTATIC COLORECTAL-CANCER; GROWTH-FACTOR RECEPTOR; 1ST-LINE TREATMENT; PHASE-III; TUMOR XENOGRAFTS; MUTATIONS; SURVIVAL; EFFICACY; THERAPY;
D O I
10.1158/1078-0432.CCR-13-3385
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To explore in a panel of patient-derived xenograft models of human non-small cell lung cancer (NSCLC) whether high EGFR expression, was associated with cetuximab activity. Experimental Design: NSCLC patient-derived xenograft models (n - 45) were implanted subcutaneously into panels of nude mice and randomization cohorts were treated with either cetuximab, cisplatin, cisplatin plus cetuximab, vehicle control, or else were left untreated. Responses according to treatment were assessed at week 3 by analyzing the relative change in tumor volume and an experimental analogue of the Response Evaluation Criteria in Solid Tumors (RECIST) guidelines. An EGFR IHC score was calculated for each patient-derived xenograft model and response was assessed according to EGFR expression level. Results: When tumors were stratified into high and low EGFR expression groups (IHC score threshold 200; scale 0-300), a stronger antitumor activity was seen in the high EGFR expression group compared with the low EGFR expression group in both the cetuximab monotherapy and cisplatin plus cetuximab combination therapy settings. For tumors treated with cisplatin plus cetuximab, the objective response rate was significantly higher in the high EGFR expression group compared with the low EGFR expression group (68% vs. 29%). Objective response rates were similar in high and low expression groups for tumors treated with cisplatin alone (27% vs. 24%, respectively). Conclusion: Cetuximab activity in NSCLC patient-derived xenograft models was demonstrated clearly only in tumors that expressed high levels of EGFR, as defined by an IHC score of >= 200. (C) 2014 AACR.
引用
收藏
页码:4478 / 4487
页数:10
相关论文
共 32 条
  • [1] HER2 Testing in Gastric Cancer
    Albarello, Luca
    Pecciarini, Lorenza
    Doglioni, Claudio
    [J]. ADVANCES IN ANATOMIC PATHOLOGY, 2011, 18 (01) : 53 - 59
  • [2] Wild-type KRAS is required for panitumumab efficacy in patients with metastatic colorectal cancer
    Amado, Rafael G.
    Wolf, Michael
    Peeters, Marc
    Van Cutsem, Eric
    Siena, Salvatore
    Freeman, Daniel J.
    Juan, Todd
    Sikorski, Robert
    Suggs, Sid
    Radinsky, Robert
    Patterson, Scott D.
    Chang, David D.
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (10) : 1626 - 1634
  • [3] [Anonymous], CLIN ADV HEMATOL S1
  • [4] A Molecularly Annotated Platform of Patient-Derived Xenografts ("Xenopatients") Identifies HER2 as an Effective Therapeutic Target in Cetuximab-Resistant Colorectal Cancer
    Bertotti, Andrea
    Migliardi, Giorgia
    Galimi, Francesco
    Sassi, Francesco
    Torti, Davide
    Isella, Claudio
    Cora, Davide
    Di Nicolantonio, Federica
    Buscarino, Michela
    Petti, Consalvo
    Ribero, Dario
    Russolillo, Nadia
    Muratore, Andrea
    Massucco, Paolo
    Pisacane, Alberto
    Molinaro, Luca
    Valtorta, Emanuele
    Sartore-Bianchi, Andrea
    Risio, Mauro
    Capussotti, Lorenzo
    Gambacorta, Marcello
    Siena, Salvatore
    Medico, Enzo
    Sapino, Anna
    Marsoni, Silvia
    Comoglio, Paolo M.
    Bardelli, Alberto
    Trusolino, Livio
    [J]. CANCER DISCOVERY, 2011, 1 (06) : 508 - 523
  • [5] Efficacy according to biomarker status of cetuximab plus FOLFOX-4 as first-line treatment for metastatic colorectal cancer: the OPUS study
    Bokemeyer, C.
    Bondarenko, I.
    Hartmann, J. T.
    de Braud, F.
    Schuch, G.
    Zubel, A.
    Celik, I.
    Schlichting, M.
    Koralewski, P.
    [J]. ANNALS OF ONCOLOGY, 2011, 22 (07) : 1535 - 1546
  • [6] Bonetti M, 2000, STAT MED, V19, P2595, DOI 10.1002/1097-0258(20001015)19:19<2595::AID-SIM562>3.0.CO
  • [7] 2-M
  • [8] Carlson Robert W, 2006, J Natl Compr Canc Netw, V4 Suppl 1, pS1
  • [9] Tumor grafts derived from women with breast cancer authentically reflect tumor pathology, growth, metastasis and disease outcomes
    DeRose, Yoko S.
    Wang, Guoying
    Lin, Yi-Chun
    Bernard, Philip S.
    Buys, Saundra S.
    Ebbert, Mark T. W.
    Factor, Rachel
    Matsen, Cindy
    Milash, Brett A.
    Nelson, Edward
    Neumayer, Leigh
    Randall, R. Lor
    Stijleman, Inge J.
    Welm, Bryan E.
    Welm, Alana L.
    [J]. NATURE MEDICINE, 2011, 17 (11) : 1514 - U227
  • [10] Establishment of Patient-Derived Non-Small Cell Lung Cancer Xenografts as Models for the Identification of Predictive Biomarkers
    Fichtner, Iduna
    Rolff, Jana
    Soong, Richie
    Hoffmann, Jens
    Hammer, Stefanie
    Sommer, Anette
    Becker, Michael
    Merk, Johannes
    [J]. CLINICAL CANCER RESEARCH, 2008, 14 (20) : 6456 - 6468