Skip to main content
OpenTrials
Not Yet Recruiting

NCT Number: NCT07487870

Radiographic Evaluation of Tumor Biology During Neoadjuvant Radiotherapy for Sarcoma

This is a single arm study in which patients will undergo MRI studies at 3 non-SOC timepoints (end of weeks 1, 3, and 5) while receiving SOC RT for their soft tissue sarcoma.

Not Yet Recruiting

Trial opening soon.

Get Notified

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Cincinnati Medical Center

Cincinnati, Ohio, 45219, United States

Location contact

Andrew Frankart

CONTACT

Andrew Frankart, MD

PRINCIPAL_INVESTIGATOR

About this study

The purpose of this research is to determine if additional imaging during radiotherapy allows for better understanding of tumor's response to radiation and better treatment planning. Modern cancer treatment has used imaging to tailor individual patient treatment and to monitor responses to therapy. Typically, assessments of tumor response to radiation are conducted by repeat imaging after completing therapy. It is known that radiation can change aspects of the tumor which impact response to therapy. These changes can potentially be seen in imaging of the tumor. The researchers in this study believe that additional imaging during treatment will allow for more personalized and better treatment for sarcoma.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients must have histologically or cytologically confirmed history of soft tissue sarcoma.
  • Plan to receive neoadjuvant radiation to a dose of 50 Gy in 25 fractions followed by surgical resection per Investigator.
  • Age ≥18 years.
  • ECOG performance status ≤2.

Exclusion criteria

  • Patients with Ewing's sarcoma and rhabdomyosarcoma.
  • Unable or unwilling to receive gadolinium-based contrast.
  • Patients who are unable or unwilling to undergo MRI studies.
  • Patients who may be unlikely or unable to be able to complete 3 additional MRI studies during the course of their 5-week radiation plan in the opinion of the PI.

Treatment and study plan

MRI

Diagnostic Test

Patients will undergo RT therapy per SOC and will receive 3 additional MRI studies at the end of RT weeks 1, 3, and 5 with an allowable window of +/- 3 days to account for delays in radiation or unforeseeable circumstances which prevent completion of MRI such as illness or weather.

Primary outcomes

  1. Feasibility measured as the percentage of study-specific MRI scans beyond standard of care which are completed

    Time frame: Treatment weeks 1, 3, and 5

    • To evaluate the feasibility of completing serial MRI studies during a course of radiation.

    a. Feasibility will be measured as the percentage of study-specific MRI scans beyond standard of care which are completed at the end of the study with greater than or equal to a 66% completion rate overall (not per patient) being considered feasible.

Study contacts

Contact information is provided by the study sponsor or research team.

Andrew Frankart, MD

CONTACT

UCCC Clinical Trials Office

CONTACT

[email protected]

513-584-7698

Sponsors and collaborators

Lead sponsor

Andrew Frankart

Other

Registry information

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Mar 23, 2026
Registry last updated
Mar 23, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.