Pilot Study of Imatinib Cetuximab Combo for H & N Cancer

Trial Title: Pilot Study of Imatinib Cetuximab Combo for H & N Cancer

NCT ID: NCT05816785

Condition: Head and Neck Cancer
Squamous Cell Carcinoma of Head and Neck

Conditions: Official terms:
Carcinoma
Carcinoma, Squamous Cell
Squamous Cell Carcinoma of Head and Neck
Cetuximab
Imatinib Mesylate

Study type: Interventional

Study phase: Early Phase 1

Overall status: Recruiting

Study design:

Allocation: N/A

Intervention model: Single Group Assignment

Primary purpose: Treatment

Masking: None (Open Label)

Intervention:

Intervention type: Drug
Intervention name: Cetuximab
Description: Week 1: loading dose of 400mg/m2; Week 2: 250mg/m2
Arm group label: Imatinib Cetuximab Combination

Intervention type: Drug
Intervention name: Imatinib
Description: 400 mg orally daily
Arm group label: Imatinib Cetuximab Combination

Summary: The goal of this clinical trial is to find if levels of a protein called AXL in tumor cells relate to how tumors respond to cetuximab (CTX) combined with imatinib in participants with head and neck cancer. This interventional study will occur in the time between diagnosis of your cancer and surgery to remove your tumor or radiation or chemoradiation treatment of your primary cancer. Participants will undergo a research blood draw and a research biopsy as part of the screening process, and will be in this research study for approximately 13 to 16 months.

Detailed description: This is a 'window of opportunity' pilot study of oral imatinib (400 mg per day) plus cetuximab (CTX) (400mg/m2 loading dose [dose 1] and 250mg/m2 [dose 2]) for patients with head and neck squamous cell carcinoma (HNSCC) undergoing definitive surgery or radiation for treatment of their cancer. The primary objective is to determine the proportion of patients with a response to imatinib plus CTX in pre-treatment and post-treatment samples obtained as part of a window of opportunity clinical study in head and neck cancer (HNC) patients.

Criteria for eligibility:
Criteria:
Inclusion Criteria: - Age > 18 years at the time of consent. - Histological confirmation of squamous cell carcinoma of the head and neck. - For those patients with oropharyngeal cancer, subjects must have either - HPV-negative status by p16 expression or HPV-DNA Expression. - HPV-positive status by p16 expression AND a >10 pack year smoking history. - Subjects must be appropriate candidates for definitive curative intent treatment, either via surgical resection, definitive radiation therapy alone, or definitive concurrent chemoradiation therapy. - For the screening research biopsy, subjects must have sufficient tumor volume (approximately 10 cc) to accommodate at minimum 2-3 core samples for the research biopsy. - For the post-treatment (CTX/Imatinib) research biopsy, subjects who are scheduled to receive definitive radiation therapy (+/- concurrent chemotherapy) are required to have sufficient tumor volume to accommodate at minimum 2-3 core samples for the research biopsy. - Demonstrate adequate organ function; all screening labs to be obtained within 28 days prior to registration. Exclusion Criteria: - Subjects with a diagnosis of nasopharyngeal carcinoma, advanced cutaneous squamous cell carcinoma of the head and neck, or salivary gland tumors are excluded from this study. - Other concurrent severe and/or uncontrolled concomitant medical conditions (e.g. active or uncontrolled infection, uncontrolled diabetes) that could cause unacceptable safety risks or compromise compliance with the protocol. - Prior chemotherapy, radiotherapy, or major surgery within 8 weeks of study enrollment or those who have not recovered (to grade ≤ 1 or baseline) from clinically significant adverse events due to agents administered more than 8 weeks earlier (alopecia and fatigue excluded). Clinical significance to be determined by the study investigator. - Subjects who have had chemotherapy or radiotherapy within 4 weeks (6 weeks for nitrosoureas or mitomycin C) prior to entering the study. - Subjects who are receiving any other investigational agents. - History of allergic reactions attributed to compounds of similar chemical or biologic composition to imatinib or CTX.

Gender: All

Minimum age: 18 Years

Maximum age: N/A

Healthy volunteers: No

Locations:

Facility:
Name: University of Wisconsin Carbone Cancer Center

Address:
City: Madison
Zip: 53792
Country: United States

Status: Recruiting

Contact:
Last name: Diana Trask

Phone: 608-236-9528
Email: trask@humonc.wisc.edu

Investigator:
Last name: Justine Bruce, MD
Email: Principal Investigator

Start date: April 18, 2023

Completion date: September 2025

Lead sponsor:
Agency: University of Wisconsin, Madison
Agency class: Other

Collaborator:
Agency: National Cancer Institute (NCI)
Agency class: NIH

Source: University of Wisconsin, Madison

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT05816785