Head and Neck Cancer
Conditions
Keywords
STAT 3 DECOY
Brief summary
The primary goal of this study is to evaluate the safety of a transcription factor decoy targeting Signal Transducer and Activator of Transcription 3(STAT3) in patients with head and neck cancer. The rationale for targeting STAT3 using this approach is to decrease STAT3-mediated gene regulation. The study has the following scientific objectives: 1. To assess the safety of a single dose of intratumoral STAT3 decoy. 2. To estimate the effect of STAT3 decoy therapy on STAT3 activation levels, STAT3-mediated gene expression, and apoptosis in treated tumors.
Detailed description
The decision to proceed with an exploratory IND study to be conducted in a phase 0 setting was based upon the expectation that the trial will involve very limited human exposure to the STAT3 decoy, and as administered, will have no therapeutic or diagnostic intent. Rather, the trial is designed to determine if intratumoral administration of the STAT3 decoy in human head and neck tumors inhibits STAT3 target gene expression. Given the cumulative evidence supporting STAT3 as a therapeutic target in cancer, and the absence of any clinical trial to date using a STAT3 inhibitor, it was felt that there would be utility in a proof of principal study to determine if the STAT3 decoy inhibits the expression of STAT3 target genes in human head and neck cancers. To support the proposed study design, the Grandis lab carried out a kinetic study in a xenograft model of SCCHN. Preliminary results demonstrated that administration of the STAT3 decoy, but not the mutant control decoy, decreased expression of STAT3 target genes (Bcl-xL and/or Cyclin D1) at time points ranging from 1 to 6 hours.
Interventions
DRUGSTAT 3 DECOY
single administration to a head and neck tumor
Sponsors
University of Pittsburgh
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Histologically confirmed diagnosis of head and neck squamous cell carcinoma(primary or recurrent) amenable to surgical resection. * ECOG performance status of 0, 1, or 2. * Adequate organ function * Age greater than or equal to 18 years * Written informed consent. * Patients with second primary lesions will be eligible for this trial. * Negative pregnancy test, nonlactating, and using effective means of contraception if childbearing potential.
Exclusion criteria
* Subjects who fail to meet the above criteria. * Subjects who are pregnant. * Subjects with an ECOG performance status \>2. * Subjects with tumors that are too small to biopsy prior to resection and reserve a portion of the resected specimen for research purposes. * Subjects who receive neoadjuvant radiotherapy and/or chemotherapy within four week prior to enrollment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evaluate the safety of a single injection. | pre and post surgery |
Secondary
| Measure | Time frame |
|---|---|
| Evaluate the biological activity by observing the consequences of STAT3 decoy administration on STAT3 activation and target gene expression in the tumor. | pre and post surgery |
Countries
United States
Outcome results
None listed