Oral Cancer, Squamous Cell Carcinoma of the Head and Neck, Squamous Cell Carcinoma of the Oral Cavity
Conditions
Keywords
cRGD-ZW800-1, fluorescence-guided surgery, image-guided surgery, fluorescence imaging, cancer
Brief summary
This is a two-staged clinical trial to investigate the feasibility of intraoperative Fluorescence Imaging (FLI) to adequately assess tumor margins in patients with oral cancer using cRGD-ZW800-1.
Detailed description
Work package I: In WP-I, the preferred dose of the agent for imaging of margins in oral cancer will be determined. The signal-to-noise ratio will be determined in dose group A (n=7), which will receive 0.05 mg/kg of the tracer, 16-20 hours before surgery. After an interim evaluation of this ratio, the second dose group B (n=7) will receive either a higher or a lower dosage (to be determined) of the tracer. After inclusion of all patients (n=14), the dose with the highest intraoperative signal-to-noise ratio will be selected. Work package II: In WP-II, an expansion cohort (n=14) will be added to the group of patients that had received the selected dose in WP-I. In this group of 21 patients, it will be determined if FLI can improve the rate of adequate surgical resection margins. As secondary research questions, the following aspects will be assessed: * sensitivity, specificity, positive and negative predictive values of FLI; * colocalization with immunohistochemistry; * change in surgical management; incremental operation time; * FLI of excised cervical lymph nodes.
Interventions
DRUGcRGD-ZW800-1.
Injection of cRGD-ZW800-1 within 48 hours before imaging/surgery
Sponsors
Erasmus Medical Center
Study design
Allocation
NON_RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
DIAGNOSTIC
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Patients with biopsy-proven squamous cell carcinoma of the oral cavity, eligible for surgical resection of the primary tumor; 2. ≥ 18 years of age; 3. Before patient registration, written informed consent must be given according to ICH/GCP, and national/local regulations; 4. Screening ECG and clinical laboratory test results are within normal limits, or if any are outside of normal limits they are considered to be clinically insignificant.
Exclusion criteria
1. Previous surgery, chemotherapy or radiotherapy to the oral cavity; 2. History of a clinically significant allergy or anaphylactic reactions to any of the components of the agent. 3. Patients pregnant or breastfeeding, lack of effective contraception in male or female patients with reproductive potential; 4. Patients with renal insufficiency (eGFR\<60); 5. Patients with a previous kidney transplantation in the medical history; 6. Immuno-compromised patients who do not have the ability to respond normally to an infection due to an impaired on weakened immune system, caused by either a pre-existing disease or concomitant medications; 7. Any condition that the investigator considers to be potentially jeopardizing the patient's well-being or the study objectives.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| WP-I: (Highest) mean tumor-to-background ratio (TBR) | up to 48 ours post-dose | Two dosages of cRGD-ZW800-1 are tested in two groups of each 7 patients. An expansion cohort (n=14) will be added to the dose group that yields the highest TBR. |
| WP-II: Rate of adequate (i.e. >5mm clear) tumor resection margins. | through histopathology, up to max 4 weeks post-op | — |
Secondary
| Measure | Time frame |
|---|---|
| WP-II: Sensitivity, specificity, positive and negative predictive values | through histopathology, up to max 4 weeks post-op |
| WP-II: Co-localization of FLI with immunohistochemistry on pathology slides | through histopathology, up to max 4 weeks post-op |
| WP-II: Percentage of extra tissue resection based on FLI-driven frozen sections | through histopathology, up to max 4 weeks post-op |
| WP-II: Operation time | through histopathology, up to max 4 weeks post-op |
| WP-II: FLI of lymph node metastases after neck dissection | through histopathology, up to max 4 weeks post-op |
Countries
Netherlands
Outcome results
None listed