Clinical trial · Interventional
Feasibility Trial of Diffusing Alpha-emitter Radiation Therapy (DaRT) for Malignant Skin & Superficial Soft Tissue Tumors
A Pilot Feasibility Trial of Diffusing Alpha-emitter Radiation Therapy (DaRT) for Malignant Skin and Superficial Soft Tissue Tumors
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This is a single-institution pilot feasibility trial in which 10 subjects will be enrolled. The primary objectives are is to explore the feasibility of delivering radiotherapy for malignant skin and superficial soft tissue tumors using DaRT (Alpha Tau Medical, Tel Aviv, Israel), a form of interstitial brachytherapy which uses a novel radioisotope delivery system, as well as to determine the frequency and severity of acute adverse events. Secondary objectives will include assessments of radiotherapy-related adverse events, tumor response, radiation safety, stability of device placement, and associations with quality of life.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Malignant Skin Tumor | Malignant Skin Neoplasm | ALIAS | 0.90 |
| Soft Tissue Tumor, Malignant | Malignant Soft Tissue Neoplasm | ALIAS | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Diffusing Alpha-emitter Radiation Therapy | Radiation | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Diffusing Alpha-emitter Radiation Therapy (DaRT)
- description
- DaRT source will be inserted using preplanned radiotherapy parameters and reassessed by volumetric imaging 2-3 weeks after placement and then removed. Tumor response to DaRT will be assessed periodically 3 months after removal.
- interventionNames
- Radiation: Diffusing Alpha-emitter Radiation Therapy
Primary outcomes (2)
- measure
- Feasibility of DaRT Delivery
- timeFrame
- 1 Day
- description
- To explore feasibility of delivering radiotherapy for malignant skin and superficial soft tissue tumors using Diffusing Alpha-emitter Radiation Therapy (DaRT). Feasibility will be determined by successful delivery of radiation by DaRT to the malignant tumor. If an attempt to place the DaRT is unsuccessful, this patient will be considered a feasibility failure. A feasibility failure may be due to inability to execute the workflow of pre-brachytherapy imaging, treatment planning, device procurement, or technical inability to place the DaRT sources into the skin and superficial soft tissue tumor. The rate of feasibility failures will be reported.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
* Malignant tumor of the skin or superficial soft tissue\*, ≥10 mm and ≤50 mm in longest dimension, with minimum tumor thickness of 4 mm
* \*Including, but after review by the Principal Investigator not limited to:
* Primary malignant tumors of the skin such as keratinocytic carcinomas (basal cell carcinoma, squamous cell carcinoma), melanocytic tumors (melanoma), soft tissue tumors (cutaneous angiosarcoma or leiomyosarcoma), and neural tumors (Merkel cell carcinoma)
* Primary malignant tumors of the superficial soft tissues such as adipocytic tumors (liposarcoma), smooth-muscle tumors (leiomyosarcoma), skeletal muscle tumors (rhabdomyosarcoma), vascular tumors (Kaposi sarcoma, angiosarcoma of soft tissue)
* Secondary malignant tumors of the skin and superficial soft tissues such as metastases from breast cancer, lung cancer, melanoma, kidney cancer and others.
* Limited treatment options for the tumor, including:
* Recurrent tumors that must have failed at least one standard therapy, which includes previous radiotherapy or surgery, OR
* Tumors in patients with metastases who will not be rendered disease-free by tumor resection, OR
* Tumors deemed inappropriate for resection by a surgeon for one of the following reasons:
* Complete tumor resection unlikely because of tumor location or size;
* Complete tumor resection deemed excessively morbid or deforming (e.g., requiring amputation of digit, lip, eyelid, ear);
* Patient with medical comorbidity contraindicating surgery; or
* Patent refusal due to anticipated morbidity
* Age \>18 years
* Eastern cooperative oncology group performance status ≤3
* Life expectancy ≥12 weeks
* Platelet count ≥50,000/mm3
* International normalized ratio of prothrombin time ≤1.8
* Creatinine ≤1.9 mg/dL
Subject Exclusion Criteria
* Contraindication to radiotherapy for skin and superficial soft tissue tumor
* Radiotherapy to the malignant skin or soft tissue tumor planned for radiotherapy within last 6 months
* Prior radiotherapy to the malignant skin or soft tissue tumor planned for radiotherapy with doses \> 60 Gy (equivalent dose in 2 Gy fractions using α/β of 8.5)
* Anticoagulation or antiplatelet medical therapy
* High probability of non-compliance with scheduled assessments as demonstrated by prior inability to complete scheduled routine clinical assessments
* Pregnancy
* Women of childbearing potential unwilling or unable to use an acceptable contraceptive method to prevent pregnancy for 1 year after brachytherapy
* Men unwilling or unable to use an acceptable contraceptive method to prevent pregnancy for 1 year after brachytherapy
* Inability to read or understand English (as QoL questionnaires are only validated in English)
* Concurrent receipt of cancer therapy which has proven effective for the malignant skin or soft tissue tumor planned for radiotherapyReferences
Publications (1)
- DERIVEDD'Andrea MA, VanderWalde NA, Ballo MT, Patra P, Cohen GN, Damato AL, Barker CA. Feasibility and Safety of Diffusing Alpha-Emitter Radiation Therapy for Recurrent or Unresectable Skin Cancers. JAMA Netw Open. 2023 May 1;6(5):e2312824. doi: 10.1001/jamanetworkopen.2023.12824. PMID 37166798