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PMID: 18223223 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Development of a real-time RT-PCR assay for detecting EGFRvIII in glioblastoma samples.

Yoshimoto K, Dang J, Zhu S, Nathanson D, Huang T, Dumont R, Seligson DB, Yong WH, Xiong Z, Rao N, Winther H, Chakravarti A, Bigner DD, Mellinghoff IK, Horvath S, Cavenee WK, Cloughesy TF, Mischel PS

Abstract

Epidermal growth factor receptor variant III (EGFRvIII) is an oncogenic, constitutively active mutant form of the EGFR that is commonly expressed in glioblastoma and is also detected in a number of epithelial cancers. EGFRvIII presents a unique antigenic target for anti-EGFRvIII vaccines and it has been shown to modulate response to EGFR kinase inhibitor therapy. Thus, detection in clinical samples may be warranted. Existing patents preclude the use of anti-EGFRvIII antibodies for clinical detection. Further, frozen tissue is not routinely available, particularly for patients treated in the community. Thus, detection of EGFRvIII in formalin-fixed paraffin-embedded (FFPE) clinical samples is a major challenge. We developed a real-time reverse transcription-PCR (RT-PCR) assay for detecting EGFRvIII in FFPE samples and analyzed 59 FFPE glioblastoma clinical samples with paired frozen tissue from the same surgical resection. We assessed EGFRvIII protein expression by immunohistochemistry using two distinct specific anti-EGFRvIII antibodies and examined EGFR gene amplification by fluorescence in situ hybridization. The FFPE RT-PCR assay detected EGFRvIII in 16 of 59 (27%) samples, exclusively in cases with EGFR amplification, consistent with the expected frequency of this alteration. The FFPE RT-PCR assay was more sensitive and specific for detecting EGFRvIII than either of the two antibodies alone, or in combination, with a sensitivity of 93% (95% confidence interval, 0.78-1.00) and a specificity of 98% (95% confidence interval, 0.93-1.00). This assay will facilitate accurate assessment of EGFRvIII in clinical samples and may aid in the development of strategies for stratifying patients for EGFRvIII-directed therapies.

MeSH Terms
ErbB Receptors/analysis Glioblastoma/chemistry Humans Paraffin Embedding Reverse Transcriptase Polymerase Chain Reaction/methods Sensitivity and Specificity
Chemicals
epidermal growth factor receptor VIII ErbB Receptors
Authors & Affiliations
18 authors, click to expand affiliations / ORCID
Yoshimoto Koji
Departments of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, CA 90095-1732, USA.
Dang Julie
Zhu Shaojun
Nathanson David
Huang Tiffany
Dumont Rebecca
Seligson David B
Yong William H
Xiong Zhenggang
Rao Nagesh
Winther Henrik
Chakravarti Arnab
Bigner Darell D
Mellinghoff Ingo K
Horvath Steve
Cavenee Webster K
Cloughesy Timothy F
Mischel Paul S
Article Info
Journal
Clinical cancer research : an official journal of the American Association for Cancer Research
Abbr.
Clin Cancer Res
ISSN
1078-0432
Published
2008-01-15
Pages
488-93
Language
English
Region
United States
NLM ID
9502500
Subset
IM
Grants
NCI NIH HHS · CA108633 · United States
NCI NIH HHS · CA119347 · United States
NCI NIH HHS · CA95616 · United States
NINDS NIH HHS · NS050151 · United States
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