MedPath

Reducing the Incidence of Symptomatic Brain Metastases With MRI Surveillance

Phase 2
Recruiting
Conditions
Nonsmall Cell Lung Cancer Stage III
Brain Metastases
Interventions
Diagnostic Test: MRI of the Brain
Other: Blood draws
Other: Quality of Life Questionnaires
Registration Number
NCT05692635
Lead Sponsor
Wake Forest University Health Sciences
Brief Summary

The purpose of this research is to see if monitoring the brain using magnetic resonance imaging (MRI) after radiation therapy will allow investigators to find cancer that has spread to the brain (brain metastases) before it causes symptoms.

Detailed Description

Primary Objective: To evaluate whether additional follow up brain MRI in patients with non-squamous stage III nonsmall cell lung cancer who were previously treated with curative intent radiation therapy reduces the rate of symptomatic brain metastasis presentation as compared to historical controls.

Secondary Objectives:

* To estimate time to brain failure in patients with non-squamous stage III nonsmall cell lung cancer previously treated with curative intent radiation therapy who undergo additional surveillance brain magnetic resonance imaging.

* To describe documented brain metastasis(es) characteristics in patients with non-squamous stage III nonsmall cell lung cancer previously treated with curative intent radiation therapy who undergo additional surveillance brain magnetic resonance imaging.

OUTLINE:

Patients undergo MRI with or without gadolinium contrast intravenously (IV) as well as blood sample collection on study.

Patients are followed for approximately 780 days from the first treatment of radiation or until death, whichever occurs first

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
60
Inclusion Criteria
  • Age ≥ 18 years of age.
  • Patients with non-squamous locally advanced lung cancer defined by American Joint Committee on Cancer (AJCC) version 8 stage IIIA, IIIB, or IIIC disease.
  • Histology described as adeno-squamous or not otherwise specified favoring squamous are eligible.
  • Patients may be enrolled before or after the start of radiation therapy but must be enrolled and have their first surveillance MRI brain at 120 +/- 10 days of their first treatment of radiation therapy for their locally advanced lung cancer. The first radiation treatment is defined as day 1.
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 - 3.
  • Epidermal growth factor receptor (EGFR) > 30 mL/min/1.73m2.
  • Patients must be eligible for a brain MRI per the Wake Forest MRI safety screening checklist questionnaire. This will be completed by a MRI imaging technician, enrolling physician, CPDM staff member, a magnetic resonance safety officer, and/or a radiologist as indicated in the form.
Exclusion Criteria
  • Known brain metastases on staging MRI.
  • Questionable findings that may represent a differential of vasculature abnormalities/stroke/ and or metastatic disease with recommended short interval follow-up are not an exclusion factor for study participation. The recommended follow-up imaging for such findings should have no bearing on the imaging schedule in this protocol, and this research protocol imaging should NOT serve as an official follow-up scan for such findings.
  • Patients who are pregnant or breastfeeding.
  • Premenopausal persons of childbearing potential must have a negative pregnancy test within 14 days of enrollment. If women are not of childbearing potential as defined by women who are menopausal female or has had a hysterectomy, bilateral oophorectomy, or medically-documented ovarian failure, they will not require a pregnancy test. Should a woman become pregnant or suspect she is pregnant while she or her partner is participating in this study, she should inform her treating physician immediately.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Surveillance MRI of the BrainMRI of the BrainBrain MRI will be performed as scheduled for up to 14 months or until detection of a brain metastasis, whichever occurs first.
Surveillance MRI of the BrainQuality of Life QuestionnairesBrain MRI will be performed as scheduled for up to 14 months or until detection of a brain metastasis, whichever occurs first.
Surveillance MRI of the BrainBlood drawsBrain MRI will be performed as scheduled for up to 14 months or until detection of a brain metastasis, whichever occurs first.
Surveillance MRI of the BrainGadoliniumBrain MRI will be performed as scheduled for up to 14 months or until detection of a brain metastasis, whichever occurs first.
Primary Outcome Measures
NameTimeMethod
Change in Central Nervous System Symptoms - Central Nervous System Symptom Scoring FormAt 4 months, 8 months, 14 months, 20 months and 26 months after first radiation therapy treatment

Symptomatic brain metastasis presentation (yes or no) will be determined for each participant. Symptomatic brain metastasis presentation anytime during follow-up will be considered a YES. Asymptomatic presentation and death during follow-up without symptomatic presentation will be considered a NO. Patients with incomplete follow-up for reasons other than death will be excluded from the analysis. The proportion with symptomatic presentation will be calculated, and compared to the historical rate of 24% using a one-sample proportion test. A symptomatic brain metastasis presentation is defined as imaging demonstrating evidence of brain metastasis(es) and a change in any given central nervous system symptom. Questions require a YES or NO answer related to symptoms. Questions that are answered YES more often would indicate a unfavorable change in central nervous system symptoms

Secondary Outcome Measures
NameTimeMethod
Collection of Information to Document Brain Metastasis(es) - Number of MetastasesAt 4 months, 8 months, 14 months, 20 months and 26 months after first radiation therapy treatment

Information collected related to the time to brain failure will include the number, size and volume of brain metastases) that are documented to help describe changes in symptoms and quality of life. Measurement in days (median) will be estimated along with a 95% confidence interval.

Collection of Information to Document Brain Metastasis(es) - Volume of MetastasesAt 4 months, 8 months, 14 months, 20 months and 26 months after first radiation therapy treatment

Information collected related to the time to brain failure will include the number, size and volume of brain metastases) that are documented to help describe changes in symptoms and quality of life. Measurement in days (median) will be estimated along with a 95% confidence interval.

Time to Brain FailureAt 4 months, 8 months, 14 months, 20 months and 26 months after first radiation therapy treatment

Time to brain failure will be defined as time in days from the start of radiation therapy to any brain failure. Time to brain failure will be estimated using the method of Kaplan and Meier. Median time to brain failure will be reported along with a 95% confidence interval.

Collection of Information to Document Brain Metastasis(es) - Size of MetastasesAt 4 months, 8 months, 14 months, 20 months and 26 months after first radiation therapy treatment

Information collected related to the time to brain failure will include the number, size and volume of brain metastases) that are documented to help describe changes in symptoms and quality of life. Measurement in days (median) will be estimated along with a 95% confidence interval.

Trial Locations

Locations (1)

Wake Forest Baptist Comprehensive Cancer Center

🇺🇸

Winston-Salem, North Carolina, United States

© Copyright 2025. All Rights Reserved by MedPath