Literature DB >> 24947928

Association of EGFR expression level and cetuximab activity in patient-derived xenograft models of human non-small cell lung cancer.

Christiane Amendt1, Eike Staub1, Manja Friese-Hamim1, Stephan Störkel2, Christopher Stroh3.   

Abstract

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. ©2014 American Association for Cancer Research.

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Year:  2014        PMID: 24947928     DOI: 10.1158/1078-0432.CCR-13-3385

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  8 in total

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2.  Inhibition of non-small cell lung cancer (NSCLC) growth by a novel small molecular inhibitor of EGFR.

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Journal:  Oncotarget       Date:  2015-03-30

3.  Role of Reactive Oxygen Species in the Abrogation of Oxaliplatin Activity by Cetuximab in Colorectal Cancer.

Authors:  Valeria Santoro; Ruochen Jia; Hannah Thompson; Anke Nijhuis; Rosemary Jeffery; Konstantinos Kiakos; Andrew R Silver; John A Hartley; Daniel Hochhauser
Journal:  J Natl Cancer Inst       Date:  2015-12-30       Impact factor: 13.506

4.  Massive parallel sequencing and digital gene expression analysis reveals potential mechanisms to overcome therapy resistance in pulmonary neuroendocrine tumors.

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6.  [18F]FDG and [18F]FLT PET for the evaluation of response to neo-adjuvant chemotherapy in a model of triple negative breast cancer.

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Journal:  PLoS One       Date:  2018-05-23       Impact factor: 3.240

7.  Systematic Review of Patient-Derived Xenograft Models for Preclinical Studies of Anti-Cancer Drugs in Solid Tumors.

Authors:  Yoshikatsu Koga; Atsushi Ochiai
Journal:  Cells       Date:  2019-05-06       Impact factor: 6.600

8.  Immuno-PET imaging for non-invasive assessment of cetuximab accumulation in non-small cell lung cancer.

Authors:  Aiko Yamaguchi; Arifudin Achmad; Hirofumi Hanaoka; Yusri Dwi Heryanto; Anu Bhattarai; Erdene Khongorzul; Rini Shintawati; A Adhipatria P Kartamihardja; Ayaka Kanai; Yumi Sugo; Noriko S Ishioka; Tetsuya Higuchi; Yoshito Tsushima
Journal:  BMC Cancer       Date:  2019-10-24       Impact factor: 4.430

  8 in total

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