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Checkpoint Inhibitor
Immunotherapy with Steroids for Brain Metastases (ACT-FAST Trial)
Phase 2
Recruiting
Research Sponsored by AHS Cancer Control Alberta
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Patients with a performance status of ECOG 0-2
Patients with histologically confirmed diagnoses of malignant melanoma, non-small cell lung cancer, renal cell carcinoma, and genitourinary carcinoma not-otherwise specified
Must not have
Known history of human immunodeficiency virus (HIV), active Hepatitis B or Hepatitis C
Active autoimmune disease requiring systemic treatment in past 2 years
Timeline
Screening 3 weeks
Treatment Varies
Follow Up upon completion of 12 month follow-up period for the final participant enrolled to the study.
Awards & highlights
No Placebo-Only Group
Summary
This trial will test whether immunotherapy is effective in treating cancer in patients also receiving treatment with steroids.
Who is the study for?
This trial is for adults with brain tumors who need steroids to reduce swelling and have started steroid therapy. They must be eligible for standard immunotherapy, have measurable brain disease, stable thyroid issues on hormones if present, and use birth control if applicable. Excluded are those with HIV, hepatitis B/C, recent autoimmune treatments or severe drug allergies.
What is being tested?
The study tests whether immunotherapy can still work effectively in patients who also require steroids due to brain metastases from cancers like melanoma or lung cancer. It compares the effects of different steroids alongside standard immune checkpoint inhibitors.
What are the potential side effects?
Potential side effects may include typical reactions to immunotherapies such as fatigue, skin reactions, inflammation of organs (like lungs or intestines), hormonal imbalances and possible worsening of underlying autoimmune diseases.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am able to get out of my bed or chair and move around.
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I have been diagnosed with melanoma, lung, kidney, or genitourinary cancer.
Select...
My cancer has spread outside of my brain.
Select...
I am eligible for standard immune therapy.
Select...
I am 18 years old or older.
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I have a brain tumor that can be measured.
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My blood, kidney, liver, and clotting tests are within normal ranges.
Select...
I am on corticosteroids for brain metastases.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I have a history of HIV, Hepatitis B, or Hepatitis C.
Select...
I have been treated for an autoimmune disease in the last 2 years.
Select...
I am taking medication that suppresses my immune system, but it's not a steroid.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ upon completion of 12 month follow-up period for the final participant enrolled to the study.
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~upon completion of 12 month follow-up period for the final participant enrolled to the study.
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Intracranial and extracranial objective response rate
Time to initiation of therapy
Secondary study objectives
Assessment of treatment safety
Mortality analyses
Patient-reported quality of life analysis
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Active Control
Group I: PrednisoneActive Control1 Intervention
Dose starting at 25 mg/day (a calculation of equipotent steroid equivalencies will be used).
Group II: DexamethasoneActive Control1 Intervention
Dose starting at 4 mg daily (for patients randomized to the Dexamethasone arm).
Find a Location
Who is running the clinical trial?
AHS Cancer Control AlbertaLead Sponsor
182 Previous Clinical Trials
26,811 Total Patients Enrolled
Media Library
Research Study Groups:
This trial has the following groups:- Group 1: Prednisone
- Group 2: Dexamethasone
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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