Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05733949

Spatiotemporal Stereotactic Body Radiation Therapy for the Treatment of Patients With Polymetastatic Solid Tumors

Led by City of Hope Medical Center · Updated on 2025-06-17

20

Participants Needed

1

Research Sites

232 weeks

Total Duration

On this page

Sponsors

C

City of Hope Medical Center

Lead Sponsor

N

National Cancer Institute (NCI)

Collaborating Sponsor

AI-Summary

What this Trial Is About

This clinical trial evaluates the safety and effectiveness of spatiotemporal stereotactic body radiation therapy (ST-SBRT) in treating patients with solid tumors that have spread to other parts of the body (polymetastatic). SBRT uses special equipment to position a patient and deliver radiation to tumors with high precision. This method may kill tumor cells with fewer doses over a shorter period and cause less damage to normal tissue. ST-SBRT is designed to deliver radiation directly to the core of the tumor, while keeping the radiation exposure of the area around the tumor at minimal dosage.

CONDITIONS

Official Title

Spatiotemporal Stereotactic Body Radiation Therapy for the Treatment of Patients With Polymetastatic Solid Tumors

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Provided informed consent and assent if required
  • Age 18 years or older
  • Karnofsky performance status greater than 60
  • Polymetastatic disease with more than 5 lesions and at least one lesion larger than 2.0 cm
  • Limited treatment options and ineligible for or progressing under standard systemic therapy
  • Intervention can be administered without exceeding dose constraints
  • Brain metastases treated prior to enrollment with stable MRI findings 3 months after treatment
  • Spinal cord metastases allowed if treatment completed
  • Prior radiotherapy allowed if dose constraints are met
  • Life expectancy of 3 months or more
  • Off systemic therapy at least one month before and after study intervention
Not Eligible

You will not qualify if you...

  • Investigator judgment that patient is unsuitable or unlikely to comply with study procedures
  • Not eligible for SBRT after radiation oncologist review
  • Serious medical conditions preventing radiotherapy
  • Unable to undergo CT scan
  • Pregnant or breastfeeding women; females of childbearing potential must have negative pregnancy test within 72 hours before therapy
  • On active systemic therapy
  • May not comply with study procedures or feasibility requirements

AI-Screening

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Trial Site Locations

Total: 1 location

1

City of Hope Medical Center

Duarte, California, United States, 91010

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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