Ipilimumab for Head and Neck Cancer Patients
Primary Purpose
Squamous Cell Carcinoma of the Head and Neck
Status
Active
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Intratumoral Ipilimumab
Sponsored by
About this trial
This is an interventional treatment trial for Squamous Cell Carcinoma of the Head and Neck focused on measuring Immunotherapy, Yervoy, Head and neck cancer, Pre-operative
Eligibility Criteria
Inclusion Criteria:
- Patients with SCCHN who are planned for surgical resection and in the opinion of the surgeon are able to safely undergo tissue biopsy plus intratumoral (IT) injection in advance, with special consideration given to risk of occlusion or compression of airway or major vessels in the neck, secondary to tumor swelling, or erosion into a major vessel in the case of necrosis.
- Age 18 years or above with ability to give informed consent, comply with the protocol and sign a study-specific consent document. Patients with history of psychiatric illness must be judged by the investigator as able to understand the investigational nature and risks associated with the therapy.
- Any Eastern Cooperative Oncology Group (ECOG) performance status deemed suitable by investigator for requirements of study, to potentially include incisional office biopsy of lesion, or image guided multiple 18g core needle biopsies (5 minimum) by interventional radiology, followed immediately by direct injection of lesion with drug.
- Patients must have blood test results within protocol-specified parameters
- Men must agree to not attempt to become a new father for a total of 165 days post-treatment completion
- Women must agree not to become pregnant for a total of 105 days post treatment completion
Exclusion Criteria:
- Any clinical factors such as bleeding, active infection, colitis history or psychiatric factors that in the judgment of the investigator would preclude safe participation and compliance with study procedures.
- Need for chronic maintenance oral steroids ≥ 20mg prednisone daily equivalent; inhaled steroids are acceptable.
- History of or current active autoimmune diseases, [e.g. including but not limited to inflammatory bowel diseases (IBD), rheumatoid arthritis, autoimmune thyroiditis, autoimmune hepatitis, systemic sclerosis (scleroderma and variants), systemic lupus erythematosus, autoimmune vasculitis, autoimmune neuropathies (such as Guillain-Barre syndrome), which in the judgment of the investigator pose an active and significant risk. Vitiligo and adequately controlled endocrine deficiencies such as hypothyroidism are not exclusionary.]
- Infectious diseases including human immunodeficiency virus (HIV), Hepatitis B virus (HBV) and hepatitis C virus (HCV).
- Patients who have had a history of acute diverticulitis, intra-abdominal abscess, GI obstruction and abdominal carcinomatosis which are known risk factors for bowel perforation, and in the judgment of the investigator still pose an active risk.
Sites / Locations
- Portland Providence Medical Center
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Intratumoral Ipilimumab
Arm Description
Patients receive a 3mg intratumoral injection of ipilimumab during a biopsy procedure.
Outcomes
Primary Outcome Measures
Surgery delay
The percentage of patients with surgery delayed possibly related to the study drug.
Secondary Outcome Measures
Feasibility of paired tissue sample acquisition
The number of tissue samples that can be collected which were: biopsied, injected, and resected.
Acceptance of study
The screening-to-enrollment ratio will be calculated.
Full Information
NCT ID
NCT02812524
First Posted
June 14, 2016
Last Updated
January 8, 2023
Sponsor
Providence Health & Services
Collaborators
Bristol-Myers Squibb
1. Study Identification
Unique Protocol Identification Number
NCT02812524
Brief Title
Ipilimumab for Head and Neck Cancer Patients
Official Title
Intratumoral Ipilimumab in Head and Neck Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
January 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
November 18, 2016 (Actual)
Primary Completion Date
September 21, 2019 (Actual)
Study Completion Date
November 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Providence Health & Services
Collaborators
Bristol-Myers Squibb
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study is for patients with squamous cell carcinoma of the head and neck (SCCHN). This study will test the feasibility of the administration of intratumoral injections of ipilimumab prior to surgical resection, and the immune system response to treatment.
Detailed Description
This study will test intratumor microdosing of ipilimumab (antagonistic antibody directed to Cytotoxic T-Lmphocyte-Associated Protein 4 [CTLA-4]) 7-10 days prior to planned surgical resection of tumor and involved lymph nodes in patients with SCCHN. Tissue, peripheral blood, saliva and stool samples will be obtained for immunologic end points. The primary objective is to assess safety, as determined by the number of surgeries that are delayed.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Squamous Cell Carcinoma of the Head and Neck
Keywords
Immunotherapy, Yervoy, Head and neck cancer, Pre-operative
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
18 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Intratumoral Ipilimumab
Arm Type
Experimental
Arm Description
Patients receive a 3mg intratumoral injection of ipilimumab during a biopsy procedure.
Intervention Type
Drug
Intervention Name(s)
Intratumoral Ipilimumab
Other Intervention Name(s)
Yervoy, BMS734016, MDX-010
Intervention Description
Patients with a planned resection of SCCHN will have a biopsy procedure 7-10 days prior to surgery and receive an injection of ipilimumab directly into a tumor.
Primary Outcome Measure Information:
Title
Surgery delay
Description
The percentage of patients with surgery delayed possibly related to the study drug.
Time Frame
7-10 Days
Secondary Outcome Measure Information:
Title
Feasibility of paired tissue sample acquisition
Description
The number of tissue samples that can be collected which were: biopsied, injected, and resected.
Time Frame
7-10 Days
Title
Acceptance of study
Description
The screening-to-enrollment ratio will be calculated.
Time Frame
28 Days
Other Pre-specified Outcome Measures:
Title
Failure rate of planned laboratory assays
Description
The percentage of assays achieving a result.
Time Frame
7-10 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients with SCCHN who are planned for surgical resection and in the opinion of the surgeon are able to safely undergo tissue biopsy plus intratumoral (IT) injection in advance, with special consideration given to risk of occlusion or compression of airway or major vessels in the neck, secondary to tumor swelling, or erosion into a major vessel in the case of necrosis.
Age 18 years or above with ability to give informed consent, comply with the protocol and sign a study-specific consent document. Patients with history of psychiatric illness must be judged by the investigator as able to understand the investigational nature and risks associated with the therapy.
Any Eastern Cooperative Oncology Group (ECOG) performance status deemed suitable by investigator for requirements of study, to potentially include incisional office biopsy of lesion, or image guided multiple 18g core needle biopsies (5 minimum) by interventional radiology, followed immediately by direct injection of lesion with drug.
Patients must have blood test results within protocol-specified parameters
Men must agree to not attempt to become a new father for a total of 165 days post-treatment completion
Women must agree not to become pregnant for a total of 105 days post treatment completion
Exclusion Criteria:
Any clinical factors such as bleeding, active infection, colitis history or psychiatric factors that in the judgment of the investigator would preclude safe participation and compliance with study procedures.
Need for chronic maintenance oral steroids ≥ 20mg prednisone daily equivalent; inhaled steroids are acceptable.
History of or current active autoimmune diseases, [e.g. including but not limited to inflammatory bowel diseases (IBD), rheumatoid arthritis, autoimmune thyroiditis, autoimmune hepatitis, systemic sclerosis (scleroderma and variants), systemic lupus erythematosus, autoimmune vasculitis, autoimmune neuropathies (such as Guillain-Barre syndrome), which in the judgment of the investigator pose an active and significant risk. Vitiligo and adequately controlled endocrine deficiencies such as hypothyroidism are not exclusionary.]
Infectious diseases including human immunodeficiency virus (HIV), Hepatitis B virus (HBV) and hepatitis C virus (HCV).
Patients who have had a history of acute diverticulitis, intra-abdominal abscess, GI obstruction and abdominal carcinomatosis which are known risk factors for bowel perforation, and in the judgment of the investigator still pose an active risk.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rom S Leidner, MD
Organizational Affiliation
Providence Health & Services
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
R. Bryan Bell, MD, DDS
Organizational Affiliation
Providence Health & Services
Official's Role
Principal Investigator
Facility Information:
Facility Name
Portland Providence Medical Center
City
Portland
State/Province
Oregon
ZIP/Postal Code
97213
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Links:
URL
https://oregon.providence.org/our-services/p/providence-cancer-center/
Description
Providence Cancer Center
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Ipilimumab for Head and Neck Cancer Patients
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