Status:
NOT_YET_RECRUITING
Alpha Radiation Emitters Device for the Treatment of Primary and Recurrent Squamous Cell Carcinoma of the Vulva (DaRT).
Lead Sponsor:
Alpha Tau Medical LTD.
Conditions:
Carcinoma of the Vulva
Recurrent Carcinoma of the Vulva
Eligibility:
FEMALE
18-120 years
Phase:
NA
Brief Summary
A unique approach for cancer treatment employing intratumoral diffusing alpha radiation emitter device for the treatment of Primary and Recurrent Squamous Cell Carcinoma of the Vulva.
Detailed Description
This is an prospective Open label, single arm, multi center, interventional study treatment of Primary and Recurrent Squamous Cell Carcinoma of the Vulva .The study objectives are to collect data on t...
Eligibility Criteria
Inclusion
- Histologically confirmed newly diagnosed or recurrent (local) vulva SCC with or without distant metastases within 12 months
- Tumor size ≤ 7 centimeters in the longest diameter.
- Targeted lesion must be technically amenable for complete coverage (including margins) by the Alpha DaRT sources.
- Measurable target according to RECIST v1.1
- Interstitial implant indication validated by multidisciplinary team.
- ECOG Performance Status ≤3.
- Life expectancy ≥6 months.
- Women Age ≥18
- Willing and have the ability to provide signed Informed Consent.
- Willing to use an acceptable contraceptive method to prevent pregnancy for 3 months after RT.
- Blood tests values:
- Leucocytes ≥3000mm3,
- Absolute neutrophil count ≥1500mm3,
- Platelets ≥100,000 mm3,
- Total bilirubin ≤ 1.5xULN,
- AST, SGOT, SGPT ≤2.5xULN, If Alkaline Phosphatase ≤ 4xULN, then transaminases are normal.
- Creatinine ≤ 2.0xULN.
- INR or Prothrombin time ≤1.5xULN.
Exclusion
- Concomitant chemotherapy or immunotherapy within the past 4 weeks
- Fit for surgical exploration unless the patient refuses surgery
- Known hypersensitivity to any of the components of the treatment.
- Patients undergoing systemic immunosuppressive therapy excepting intermittent, brief use of systemic corticosteroids.
- Longest tumor diameter \>7 cm.
- Clinically significant cardiovascular disease, e.g. cardiac failure of New York Heart Association classes III-IV, uncontrolled coronary artery disease, cardiomyopathy, uncontrolled arrhythmia, uncontrolled hypertension, or history of myocardial infarction in the last 12 months.
- Patients with uncontrolled intercurrent illnesses including, but not limited to an active infection requiring systemic therapy (not including cholangitis) or a known psychiatric or substance abuse disorder(s) that would interfere with cooperation with the requirements of the trial or interfere with the study endpoints.
- Has a known additional malignancy that is progressing or requires active treatment. Exceptions include basal cell carcinoma of the skin or squamous cell carcinoma of the skin that has undergone potentially curative therapy or in situ cervical cancer.
- Patient requires treatment not specified in this protocol which may conflict with the endpoints of this study including evaluation of response or toxicity of Alpha DaRT.
- Volunteers participating in another interventional study in the past 30 days which might conflict with the endpoints of this study or the evaluation of response or toxicity of Alpha DaRT.
- High probability of protocol non-compliance (in opinion of investigator).
- Breastfeeding women or women of childbearing potential unwilling or unable to use an acceptable contraceptive method to prevent pregnancy for 3 months after RT.
- Subjects not willing to sign an informed consent
Key Trial Info
Start Date :
April 1 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 1 2026
Estimated Enrollment :
10 Patients enrolled
Trial Details
Trial ID
NCT06202339
Start Date
April 1 2024
End Date
December 1 2026
Last Update
January 31 2024
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