Minibeam Radiation Therapy With Tungsten Slit Collimator for the Treatment of Recurrent or Metastatic Skin or Soft Tissue Tumors, MBRT1 Trial

Last updated: December 2, 2025
Sponsor: Mayo Clinic
Overall Status: Active - Recruiting

Phase

N/A

Condition

Sarcoma

Skin Cancer

Molluscum Contagiosum

Treatment

Biopsy Procedure

Computed Tomography

Medical Device Usage and Evaluation

Clinical Study ID

NCT07062003
GMROR2471
24-004810
GMROR2471
NCI-2025-04429
  • Ages > 18
  • All Genders

Study Summary

This clinical trial tests the safety and best dose of minibeam radiation therapy (MBRT) with a tungsten slit collimator for treating patients with skin or soft tissue tumors that have come back after a period of improvement (recurrent) or that spread from where they first started (primary site) to other places in the body (metastatic). Radiation therapy uses high energy x-rays, particles, or radioactive seeds to kill tumor cells and shrink tumors. Tungsten is an extremely dense metal and is commonly used for blocking x-rays for minimum radiation exposure. A tungsten slit collimator is a device that separates an initially wide beam of x-rays into several very narrow individual beams of radiation. As radiation passes through the collimator, the radiation hits regions of solid tungsten and is blocked. In the open slit regions, radiation passes through to the intended target/tumor area defined by the physician. The tungsten slit collimator then selectively blocks portions of the radiation to create an alternating pattern of higher "peak" and lower "valley" radiation dose regions. These narrow beams of radiation are referred to as "minibeams" and the general approach referred to as MBRT.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Age ≥ 18 years

  • Histologically confirmed malignancy

  • Primary, recurrent, or metastatic skin or superficial soft tissue tumor amenable topalliative orthovoltage radiotherapy

  • Anticipated life expectancy ≥ 30 days and anticipated capacity for follow up for ≥ 30 days

  • Negative pregnancy test done ≤ 28 days prior to registration, for biological womenof childbearing potential only

  • Willing to provide written informed consent

  • Willing to allow baseline and follow up photograph acquisition for response andtoxicity assessment

  • Willing and able to return to enrolling institution for follow-up during the activemonitoring phase of the study

  • Willing to provide blood and tissue samples for correlative research purposes

Exclusion

Exclusion Criteria:

  • Hematologic, germ cell, or any other tumor that the investigational team would deemto have a high likelihood of clinical complete response with standard palliativeradiotherapy (8 Gy in 1, 30 Gy in 10, etc.)

  • COHORT A (INTACT SKIN) ONLY: Prior radiotherapy targeting the lesion presenting fortreatment or prior adjacent radiotherapy if > 10 Gy overlaps with a portion of theplanned target

  • Treatment with a B-Raf proto-oncogene, serine/threonine kinase (BRAF) inhibitor,monoclonal antibodies targeting vascular endothelial growth factor (VEGF) (bevacizumab or ramucirumab) or small molecule inhibitors inhibiting VEGF within thelast 2 weeks or planned treatment with BRAF inhibitor within 4 weeks after radiation

  • Treatment with an investigational drug therapy within 2 weeks prior to or 4 weeks (the DLT monitoring period) after MBRT

  • Any tumor with direct extension into the spine such that targeting the spine/spinalcord could not be avoided

Study Design

Total Participants: 60
Treatment Group(s): 5
Primary Treatment: Biopsy Procedure
Phase:
Study Start date:
August 11, 2025
Estimated Completion Date:
August 01, 2028

Study Description

PRIMARY OBJECTIVE:

I. To determine the maximum tolerated dose (MTD) of MBRT and describe the adverse events of treatment.

SECONDARY OBJECTIVE:

I. To assess the ability to maintain a distinct differential between peak and valley doses using film dosimetry.

EXPLORATORY OBJECTIVES:

I. To estimate the rate of freedom from local progression at 6 and 12 months after the start of MBRT.

II. To evaluate pre-treatment and post-treatment differential abundance of peripheral blood immune cell populations and their activation markers.

III. Explore germline and somatic mutations in homologous recombination (HR) genes and their association with freedom from local progression.

IV. Quantify the immune phenotypes and cell signaling in the tumor microenvironment pre-MBRT and post-MBRT using bulk ribonucleic acid (RNA)-sequencing (seq) data.

OUTLINE:

Patients undergo MBRT with a tungsten slit collimator over 2-3 fractions on study. Patients also undergo standard of care CT simulation on study and undergo collection of blood samples and punch or core biopsy throughout the study.

After completion of study treatment, patients are followed up at weeks 2, 4, and 12, and months 6, 9, and 12.

Connect with a study center

  • Mayo Clinic in Rochester

    Rochester, Minnesota 55905
    United States

    Site Not Available

  • Mayo Clinic in Rochester

    Rochester 5043473, Minnesota 5037779 55905
    United States

    Active - Recruiting

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