Using Xe MRI to Guide Radiation Therapy for Lung Cancer

Part of paid clinical trials in Iowa City, Iowa.

Sponsor
Sean Fain
Study ID
NCT06925295
Phase
PHASE2
Status
Recruiting

Conditions

  • Imaging Techniques

Eligibility Criteria

Sex
ALL
Age
18 Years - 80 Years
Healthy Volunteers
Not accepted

Interventions

  • Xenon MRI — DRUG
    MRI with Xenon used for contrast
  • Pulmonary Function Testing — DIAGNOSTIC_TEST
    Pulmonary function testing will include spirometry, lung volumes, DLCO and oscillometry
  • Quality of Life Questionnaire — OTHER
    European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30+QLQ-LC29)
  • Medical Research Council Dyspnea score — OTHER
    modified Medical Research Council Dyspnea score (mMRC Dyspnea)
  • St. George's Respiratory Questionnaire — OTHER
    St. George's Respiratory Questionnaire (SGRQ)
  • Blood Biomarkers — DIAGNOSTIC_TEST
    blood biomarkers of inflammation and injury (e.g. Angiopoetin-2, Interleukin-6, myofibroblast activity, BPD4)

Study Details

The purpose of this research study is to explore using MRI scans with xenon to better image lung function, how lung function changes after radiation therapy, and to guide radiation therapy away from parts of the lung that have good function. This project is foundational to performing additional studies to establish if novel MRI imaging can serve as a guidance tool for lung cancer radiation treatment.

Key Dates

Start date
Aug 30, 2025
Status verified
Dec 2025
Primary completion
Jan 31, 2027
Completion
Jan 31, 2027

Study Design

Enrollment
15 participants (estimated)
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC

Arms

  • Experimental: Technical Development Arm
    Lung cancer patients who will undergo standard-of-care stereotactic body radiation therapy (SBRT).
  • Experimental: Implementation Arm
    Lung cancer patients who will undergo SBRT plans that were functionally adapted to avoid highly functioning lung based on Xe MRI.

Primary Outcome Measure

The incidence of PFT evidence of radiation pneumonitis and lung function change on spirometry [ Time Frame: Baseline Visit, periprocedural, 1 month follow up visit, and 6 month follow up visit.. ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
University of IowaIowa CityIowa52242
Eric Bruening
319 678 2385
Sean Fain, PhD (PRINCIPAL_INVESTIGATOR)

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