Standard-Dose or High-Dose Erlotinib Hydrochloride Before Surgery in Treating Patients With Head and Neck Cancer

PRIMARY OBJECTIVES:

I. To determine the effects of erlotinib (erlotinib hydrochloride) 150 mg/day (standard dose)
and 200 mg/day or 300 mg/day (high-dose) on the phosphorylation of AKT protein downstream
from epidermal growth factor receptor (EGFR).

SECONDARY OBJECTIVES:

I. To assess the safety and tolerability of erlotinib 150 mg/day (standard dose) and 200
mg/day or 300 mg/day (high-dose).

II. To correlate the effects of erlotinib on the phosphorylation of AKT with the
immunohistochemical expression level of EGFR and the level of amplification of the EGFR gene
as determined by fluorescent in situ hybridization (FISH).

III. To evaluate the preliminary response rate with a short course of erlotinib.

IV. To evaluate changes in the activation status of proteins downstream from EGFR and other
receptor tyrosine kinases and in markers of epithelial to mesenchymal transition.

V. To evaluate changes in blood-based biomarkers. VI. To evaluate the effects of a higher
dose of erlotinib (300 mg/day) in current smokers.

TERTIARY OBJECTIVES:

I. To evaluate EGFR gene copy number by fluorescent in situ hybridization. II. To evaluate
immunohistochemistry, western blotting and reverse phase protein lysate arrays to assess the
activation (usually phosphorylation) status of other downstream proteins from EGFR and other
receptor tyrosine kinases (these will include, but are not restricted to: EGFR itself,
phosphatidylinositol 3 Kinase [PI3K], AKT, mammalian target of rapamycin [mTOR], glycogen
synthase kinase 3 [GSK3], p70 ribosomal S6 kinase [p70S6K], S6, 4E-binding protein 1[4E-BP1],
MEK1/2, mitogen-activated protein kinase [MAPK], p38, -c-Jun N-terminal kinase [JNK],
insulin-like growth factor 1 receptor [IGF-1R], IGF-2R, mesenchymal epithelial transition
[MET], hypoxia-inducible factor [HIF]) both before and after treatment with erlotinib.

III. To evaluate immunohistochemical expression levels of markers of epithelial to
mesenchymal transition (these will include, but are not restricted to: e-cadherin and
vimentin).

IV. To study blood-based biomarkers of interest, which will include (but are not restricted
to): trough levels of erlotinib and its metabolites, a panel of 59 cytokine and angiogenic
factors measured by available Luminex multiplex beads kits (Bio-Plex 27-Plex & 23-Plex Kits
[Bio-Rad, Hercules, CA] and Human cardiovascular disease [CVD] Biomarker Panel 1 kit [Linco
Research, Inc., St, Charles, MO]) as well as validated enzyme-linked immunosorbent assays for
soluble vascular endothelial growth factor receptor 1(VEGFR1), VEGFR2 (Invitrogen, Carlsbad,
CA), total IGF-1, IGF-2, insulin-like growth factor-binding protein (IGFBP3) (DSL, Webster,
TX), and osteopontin (R&D Systems, Minneapolis, MN).

V. To evaluate whole genome sequencing and/or sequencing of specific genes of interest,
analysis of gene copy number, messenger ribonucleic acid (mRNA) expression profiles,
non-coding RNA expression profiles, single nucleotide polymorphisms, deoxyribonucleic acid
(DNA) methylation profiles, immunohistochemistry of proteins of interest to head and neck
cancer biology, and proteomics in tumor tissue and/or normal tissue (including blood) before
and after treatment with erlotinib.

OUTLINE: Patients are randomized to 1 of 2 treatment arms.

ARM I: Patients receive standard-dose erlotinib hydrochloride orally (PO) once daily (QD) for
2-3 weeks (up to 8 weeks if surgery is delayed).

ARM II: Patients receive high-dose erlotinib hydrochloride PO QD for 2-3 weeks (2-8 weeks for
current smokers or up to 8 weeks if surgery is delayed).

After completion of study treatment, patients are followed up within 30 days.

Inclusion Criteria:

- Patients with histologically confirmed cancer of the head and neck; patients with
salivary gland tumors and squamous cell carcinomas of the skin are also eligible;
(note: any patient with a diagnosis of aggressive squamous cell carcinoma of the skin
and determined to be surgically resectable will be considered for eligibility; these
patients are typically seen in the head & neck surgery clinic and decisions for study
consideration will be based on consultations with the department of head & neck
surgery)

- The patient must have biopsy-accessible disease

- Patients must be surgical candidates (either definitive or palliative setting)

- Patients may have received prior therapy including cytotoxic chemotherapy (e.g.
platinum drugs and taxanes) and radiation therapy

- Patients must have a performance score (Eastern Cooperative Oncology Group [ECOG]) of
0-2

- Peripheral granulocyte count of >= 1,000/mm^3

- Platelet count of >= 50,000/mm^3

- Bilirubin =< 1.5 times the upper limit of normal (ULN)

- Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) must be =< 2 x the
ULN

- Alkaline phosphatase must be =< 2 x ULN

- Serum creatinine =< 1.5 x ULN

- Ability to understand and the willingness to sign a written informed consent document
indicating that they are aware of the investigational nature of the study, in keeping
with institutional policy

- Women of childbearing potential must agree to use adequate contraception (hormonal or
barrier method of birth control; abstinence) prior to study entry and for the duration
of study participation; childbearing potential will be defined as women who have had
menses within the past 12 months, who have not had tubal ligation or bilateral
oophorectomy; should a woman become pregnant or suspect that she is pregnant while
participating in this study, she should inform her treating physician immediately; the
patient, if a man, agrees to use effective contraception or abstinence

Exclusion Criteria:

- Patients with prior exposure to small molecule tyrosine kinase inhibitors or
EGFR-targeted antibodies within the past 6 months

- Patients for whom, in the opinion of the treating surgeon, the administration of
erlotinib would cause a deleterious delay in surgical treatment

- Patients with uncompensated congestive cardiac failure

- Patients with an organ allograft

- Patients with a serious concurrent infection or illness including, but not limited to,
unstable angina pectoris, cardiac arrhythmia, or psychiatric illness that could limit
compliance with study requirements

- Female patients who are pregnant or breastfeeding

- Patients currently on chemotherapy, immunotherapy, or therapy with monoclonal
antibodies or other investigational agents with anti-tumor activity