Phase I/II Study of Postoperative Adjuvant Chemoradiation for Advanced-Stage Cutaneous Squamous Cell Carcinoma of the Head and Neck (cSCCHN)

Withdrawn before enrolling · Phase 1/Phase 2 · Has a placebo group

Conditions studied: Recurrent Skin Cancer, Recurrent Squamous Cell Carcinoma of the Lip and Oral Cavity, Squamous Cell Carcinoma of the Skin, Stage III Squamous Cell Carcinoma of the Lip and Oral Cavity, Stage IVA Squamous Cell Carcinoma of the Lip and Oral Cavity, Stage IVB Squamous Cell Carcinoma of the Lip and Oral Cavity

In brief

This phase I/II trial studies the side effects and best dose of linsitinib when given together with erlotinib hydrochloride and radiation therapy after surgery in treating patients with advanced or recurrent head and neck cancer. Erlotinib hydrochloride and linsitinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Radiation therapy uses high-energy x-rays to kill tumor cells. Giving radiation therapy together with erlotinib hydrochloride and linsitinib may kill more tumor cells. Giving these treatments after surgery may kill any tumor cells that remain after surgery.

Key facts

Study ID

NCT01465815

Run by

OHSU Knight Cancer Institute

People needed

0

Starts

2011-12-01

Expected to finish

2013-09-01

Last updated by the study team

2014-11-19

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients must have primary or recurrent advanced-stage (III/IV) squamous cell carcinoma of the skin of the face, ear, scalp or neck or of the lip
• A biopsy or preserved representative tumor block is required to confirm the diagnosis
• Patients must be surgical candidates with resectable disease; macroscopic complete resection of all tumor must be planned with curative intent
• Patients must be willing to receive postoperative radiation therapy and treatment with study drugs
• Both men and women and members of all races and ethnic groups will be included
• Life expectancy of greater than 12 months
• Eastern Cooperative Oncology Group (ECOG) performance status =< 2
• Absolute neutrophil count >= 1,500/microliter(uL)
• Hemoglobin >= 9 g/dL
• Platelets >= 100,000/uL
• International normalized ratio (INR) < institutional upper limit of normal (ULN)
• Total bilirubin =< 1.5 x institutional ULN
• Aspartate aminotransferase (AST) serum glutamic oxaloacetic transaminase (SGOT)/alanine aminotransferase (ALT) serum glutamic pyruvic transaminase (SGPT) =< 2.5 X institutional ULN
• Creatinine =< 1.5 X institutional ULN
• Fasting blood glucose < 125 mg/dL at baseline
• Patients-both males and females-with reproductive potential (i.e., menopausal for less than 1 year and not surgically sterilized) must practice effective contraceptive measures throughout the study; women of childbearing potential must provide a negative pregnancy test (serum or urine) within 14 days prior to registration
• Ability to understand and the willingness to sign a written informed consent document

You may not qualify if…

• Patients with known distant metastasis
• Patients who have had prior radiation treatment of the index cancer or area of disease
• Patients who have received any other investigational medication within 6 weeks of enrollment, or who are scheduled to receive an investigational drug during the course of the study
• Prior treatment with EGFR inhibitor for index cancer
• Prior treatment with an IGF-1R antagonist (small molecule inhibitor or antibody)
• Breast-feeding, pregnancy or of childbearing potential (including less than two years postmenopausal) and unable to confirm adequate contraception due to possible risk to fetus or infant
• Insulin-dependent and non-insulin dependent diabetes mellitus including any metformin or insulin use on an ongoing basis prior to enrollment
• Known severe hypersensitivity to erlotinib, other small molecule inhibitors of EGFR, or its excipients
• Hepatitis B or C infection (acute or chronic), known human immunodeficiency virus (HIV), or active uncontrolled infection, because of possible risk of lethal infection when treated with marrow suppressive therapy
• History of uncontrolled cardiac disease such as unstable angina pectoris, myocardial infarction within prior 6 months, untreated coronary artery disease, uncontrolled congestive heart failure, or cardiomyopathy with decreased ejection fraction
• Uncontrolled peptic or gastric ulcer disease or gastrointestinal bleeding within prior 6 months
• Corrected QT interval (QTc) > 450 msec; congenital long QT syndrome or previous history of QTc prolongation as a result from other medication
• Presence of left bundle branch block (LBBB); QTc with Bazett's correction that is unmeasurable, or >= 450 msec on screening electrocardiogram (EKG)
• Any concomitant medication that may cause QTc prolongation or concomitant medication that is associated with Torsades de Pointes
• Psychiatric illness/social situations that would limit compliance with study requirements
• Active smokers unwilling to quit smoking during treatment
• Use of the potent cytochrome P450 3A4 (CYP3A4) and cytochrome P450 1A2 (CYP1A2) inhibitors is not allowed; other less potent CYP3A4 and CYP1A2 inhibitors/inducers are not excluded
• Participation in another investigational trial while on this study is not allowed
• History of poorly controlled gastrointestinal disorders including acute diverticulitis, intra-abdominal abscess, gastrointestinal obstruction, Crohn's disease, ulcerative colitis or other diseases which have the potential for bowel perforation
• Other malignancies except for resected cervical cancer in situ

Where it is running

• OHSU Knight Cancer Institute — Portland, Oregon, United States

Full record on ClinicalTrials.gov

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