Head and Neck Squamous Cell Carcinoma
Conditions
Keywords
HNSCC, Nivolumab, immunotherapy
Brief summary
Each subject will participate in the trial until death, drop out, or loss-to follow-up from the time the subject signs the Informed Consent Form (ICF) through the final contact. After a screening phase of up to 28 days, each eligible subject will receive nivolumab. Two weeks after start of nivolumab the patients will receive radiotherapy (RT) to a total dose of 60 Gy, given as 1.5 Gy fractions twice daily for a total period of 4 weeks. Treatment with nivolumab will continue until disease progression, unacceptable adverse event(s), intercurrent illness that prevents further administration of treatment, Investigator's decision to withdraw the subject, noncompliance with trial treatment or procedures requirements, subject receives nivolumab for 12 months, pregnancy, or administrative reasons. After the end of treatment, each subject will be followed for 30 days for adverse event monitoring serious adverse events (SAEs) will be collected for 90 days after the end of treatment. Patients without disease progression will have follow-up visits for 4 years after end of study therapy.
Detailed description
In this study, the aim is to release the brake on the immune response by use of nivolumab, an inhibitory antibody against Programmed cell death protein 1 (PD-1). Nivolumab has shown efficacy and mild toxicity when given as monotherapy for HNSCC at a dose of 3.0 mg/kg every 2 weeks, which is the target dose in the present trial. Radiotherapy is a powerful inducer of inflammation, and the expression of Programmed death-ligand 1 (PD-L1) is known to be enhanced by inflammatory cytokines, including interferon-gamma (IFNg). Experimental evidence from mice models have shown that radiotherapy induces increased PD-L1 expression in tumor tissue. Moreover, there is evidence suggesting that HNSCC with T-cell infiltration is more sensitive to radiotherapy. There is thus a strong rationale for combing PD-1 inhibitors with radiotherapy. However, this potential remains largely unexplored in humans. The investigators consider that head-and-neck cancer is a particularly attractive entity for investigating this therapeutic combination, because of i) the high radiosensitivity of this cancer form ii) the clinical efficacy of Programmed cell death protein 1 (PD-1) inhibitors as monotherapy in early clinical trials iii) the availability of tumor biopsies for translational/biomarker research.The RT given in the present study gives considerable side effects, related to inflammation that may be enhanced by Programmed cell death protein 1 (PD-1) blockade.
Interventions
DRUGNivolumab
Nivolumab is a humanized antibody used in cancer immunotherapy.
RADIATIONRadiotherapy (RT)
Radiotherapy (RT) will be given to a total dose of 60 Gy (1,5 Gy fractions twice daily) for a total period of 4 weeks
Sponsors
Bristol-Myers Squibb
Oslo University Hospital
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Intervention model description
Exploratory
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Age 18 years or older * Recurrent or secondary primary squamous cell carcinoma originating from the oral cavity, oro/hypo-pharynx or larynx * Prior radiotherapy (46-70Gy) * Adequate newly obtained core or excisional biopsy of a recurrent tumor lesion * Measurable disease * Lesion available for biopsy during study treatment * Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1 * Life expectancy of more than 12 months * A minimum of 6 months since prior radiotherapy in the same area or minimum 4 weeks (28 days) since previous other cancer treatment * Human papillomavirus positive and negative disease allowed * Distant metastases allowed * Adequate organ function based on clinical examination and lab values * Women of childbearing potential (WOCBP) must have a negative serum or urine pregnancy test (minimum sensitivity 25 IU/L or equivalent units of HCG) within 24 hours prior to the start of study drug * Women must not be breastfeeding * WOCBP should use an adequate method to avoid pregnancy for 23 weeks (30 days plus the time required for nivolumab to undergo five half-lives) after the last dose of investigational drug * Males who are sexually active with WOCBP must agree to follow instructions for method(s) of contraception for a period of 90 days (duration of sperm turnover) plus the time required for the investigational drug to undergo five half-lives. The terminal half-life of nivolumab is up to 25 days
Exclusion criteria
* History of other prior malignancy, with the exception of curatively treated basal cell or squamous cell carcinoma of the skin, cervical cancer stage IB and stage I prostate cancer considered not necessary to treat * Disease suitable for curative salvage surgery * Treatment with any investigational medicinal product (IMP) that may interfere with the study treatment, within 4 weeks prior to first administration of study drug. * Significant cardiac, pulmonary or other medical illness that would limit activity or survival * Pregnancy or lactation. * Known hypersensitivity to any of the components of the investigational product * Patients who test positive for hepatitis B, C or HIV. * Diagnosis of immunodeficiency or medical condition requiring systemic steroids or other forms of immunosuppressive therapy * Autoimmune disease that has required systemic therapy within the past 2 years * Any reason why, in the opinion of the investigator, the patient should not participate
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence, nature, and severity of adverse events graded according to Common Terminology Criteria for Adverse Events (CTCAE) Version 4.0. | 18 months (6 months after end of treatment) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Progression-free survival (PFS) | After 12 months | defined as the time from inclusion to the time of radiographic progression (as assessed by RECIST) or death from any cause during the study |
| Objective response rate (ORR) | 3 years | defined as the proportion of patients with an objective tumor response |
| Overall survival (OS) | 5 years | defined as the time from the date of inclusion to the date of death from any cause |
| Duration of response (DOR) | 3 years | among patients with an objective response |
| Durable response rate (DRR) | 3 years | defined as the proportion of patients with an objective tumor response lasting at least 6 months |
Other
| Measure | Time frame | Description |
|---|---|---|
| Immunological response | 3 years | as assessed by gene profiling, immunohistochemistry, T cell assays, characterization of cell suspensions from tumor and peripheral blood |
| tumor evolution | 3 years | as assessed by gene profiling, immunohistochemistry, characterization of cell suspensions from tumor and peripheral blood |
Countries
Norway
Outcome results
None listed