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Randomized, placebo-controlled window trial of EGFR, Src, or combined blockade in head and neck cancer.

Authors :
Bauman JE
Duvvuri U
Gooding WE
Rath TJ
Gross ND
Song J
Jimeno A
Yarbrough WG
Johnson FM
Wang L
Chiosea S
Sen M
Kass J
Johnson JT
Ferris RL
Kim S
Hirsch FR
Ellison K
Flaherty JT
Mills GB
Grandis JR
Source :
JCI insight [JCI Insight] 2017 Mar 23; Vol. 2 (6), pp. e90449. Date of Electronic Publication: 2017 Mar 23.
Publication Year :
2017

Abstract

BACKGROUND. EGFR and Src family kinases are upregulated in head and neck squamous cell carcinoma (HNSCC). EGFR interacts with Src to activate STAT3 signaling, and dual EGFR-Src targeting is synergistic in HNSCC preclinical models. pSrc overexpression predicted resistance to the EGFR inhibitor, erlotinib, in a prior window trial. We conducted a 4-arm window trial to identify biomarkers associated with response to EGFR and/or Src inhibition. METHODS. Patients with operable stage II-IVa HNSCC were randomized to 7-21 days of neoadjuvant erlotinib, the Src inhibitor dasatinib, the combination of both, or placebo. Paired tumor specimens were collected before and after treatment. Pharmacodynamic expression of EGFR and Src pathway components was evaluated by IHC of tissue microarrays and reverse-phase protein array of tissue lysates. Candidate biomarkers were assessed for correlation with change in tumor size. RESULTS. From April 2009 to December 2012, 58 patients were randomized and 55 were treated. There was a significant decrease in tumor size in both erlotinib arms ( P = 0.0014); however, no effect was seen with dasatinib alone ( P = 0.24). High baseline pMAPK expression was associated with response to erlotinib ( P = 0.03). High baseline pSTAT3 was associated with resistance to dasatinib ( P = 0.099). CONCLUSIONS. Brief exposure to erlotinib significantly decreased tumor size in operable HNSCC, with no additive effect from dasatinib. Baseline pMAPK expression warrants further study as a response biomarker for anti-EGFR therapy. Basal expression of pSTAT3 may be independent of Src, explain therapeutic resistance, and preclude development of dasatinib in biomarker-unselected cohorts. TRIAL REGISTRATION. NCT00779389. FUNDING. National Cancer Institute, American Cancer Society, Pennsylvania Department of Health, V Foundation for Cancer Research, Bristol-Myers Squibb, and Astellas Pharma.<br />Competing Interests: Conflict of interest: The authors have declared that no conflict of interest exists.

Details

Language :
English
ISSN :
2379-3708
Volume :
2
Issue :
6
Database :
MEDLINE
Journal :
JCI insight
Publication Type :
Academic Journal
Accession number :
28352657
Full Text :
https://doi.org/10.1172/jci.insight.90449