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Clinical Trials/NCT05692635
NCT05692635
Recruiting
Phase 2

Reducing the Incidence of Symptomatic Brain Metastases With MRI Surveillance in Non-Squamous Locally Advanced Non-Small Cell Lung Cancer

Wake Forest University Health Sciences1 site in 1 country60 target enrollmentAugust 30, 2023

Overview

Phase
Phase 2
Intervention
MRI of the Brain
Conditions
Brain Metastases
Sponsor
Wake Forest University Health Sciences
Enrollment
60
Locations
1
Primary Endpoint
Change in Central Nervous System Symptoms - Central Nervous System Symptom Scoring Form
Status
Recruiting
Last Updated
last month

Overview

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

Registry
clinicaltrials.gov
Start Date
August 30, 2023
End Date
April 1, 2028
Last Updated
last month
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

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
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 -
  • Epidermal growth factor receptor (EGFR) \> 30 mL/min/1.73m
  • 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.

Arms & Interventions

Surveillance MRI of the Brain

Brain MRI will be performed as scheduled for up to 14 months or until detection of a brain metastasis, whichever occurs first.

Intervention: MRI of the Brain

Surveillance MRI of the Brain

Brain MRI will be performed as scheduled for up to 14 months or until detection of a brain metastasis, whichever occurs first.

Intervention: Blood draws

Surveillance MRI of the Brain

Brain MRI will be performed as scheduled for up to 14 months or until detection of a brain metastasis, whichever occurs first.

Intervention: Quality of Life Questionnaires

Surveillance MRI of the Brain

Brain MRI will be performed as scheduled for up to 14 months or until detection of a brain metastasis, whichever occurs first.

Intervention: Gadolinium

Outcomes

Primary Outcomes

Change in Central Nervous System Symptoms - Central Nervous System Symptom Scoring Form

Time Frame: At 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 Outcomes

  • Collection of Information to Document Brain Metastasis(es) - Number of Metastases(At 4 months, 8 months, 14 months, 20 months and 26 months after first radiation therapy treatment)
  • Collection of Information to Document Brain Metastasis(es) - Volume of Metastases(At 4 months, 8 months, 14 months, 20 months and 26 months after first radiation therapy treatment)
  • Time to Brain Failure(At 4 months, 8 months, 14 months, 20 months and 26 months after first radiation therapy treatment)
  • Collection of Information to Document Brain Metastasis(es) - Size of Metastases(At 4 months, 8 months, 14 months, 20 months and 26 months after first radiation therapy treatment)

Study Sites (1)

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