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Single vs Multi-fraction SRS Patients on Immunotherapy

MIGRAINE: Randomized trIal of Single Versus Multifraction Radiosurgery on Immunotherapy

Status
Withdrawn
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04427228
Acronym
MIGRAINE
Enrollment
0
Registered
2020-06-11
Start date
2020-06-29
Completion date
2022-12-12
Last updated
2023-08-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Brain Cancer, Brain Metastases

Brief summary

This study is meant to compare different surgical approaches to brain cancer.

Interventions

RADIATIONRadiosurgery Single Treatment

Frameless single-fraction SRS. One large treatment done on each brain tumor. 20 Gy for GTVs (or resection cavity CTVs) \< 2 cm, and 18 Gy for GTVs (or resection cavity CTVs) between 2-3 cm in the single-fraction.

RADIATIONRadiosurgery Three Treatments

Multi-fraction SRS. Three small doses done on each brain tumor. 27 Gy in 3 fractions in the multi-fraction group

Sponsors

University of Chicago
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Caregiver)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

i. Adult patients (≥ 18 years old) with an ECOG Performance Status 0-2 and a life expectancy of 3 months or more. ii. Histologically confirmed systemic malignancy with gadolinium contrast-enhanced MRI scan demonstrating 1-10 newly diagnosed intraparenchymal brain metastases. iii. Well-circumscribed, measureable intraparenchymal brain metastasis(s) with maximum tumor diameter ≤3.0 cm. If multiple metastases are present, the other(s) must not exceed 3.0 cm in maximum diameter. At least one metastasis must be ≥ 0.5 cm in maximum diameter to be considered measurable disease. iv. Negative urine or serum pregnancy test done ≤ 21 days prior to CT simulation, for women of child bearing potential only. v. Ability to understand and willingness to sign a written informed consent document. vi. Must have received immunotherapy (PD-1/PD-L1 and/or CTLA-4 inhibitor(s)) within the past 6 months or plan on receiving immunotherapy within the next 1 month. vii. Must have a Gustave Roussy Immune Score (GRIm-Score) of 0 or 1 (neutrophil-to-lymphocyte ratio \> 6 = 1 point, LDH \> Upper Limit of Normal = 1 point, and Albumin \< 3.5 g/dL = 1 point).

Exclusion criteria

i. Diagnosis of germ cell tumor or hematologic malignancy. ii. Metastases in the brain stem, midbrain, pons, medulla, or within 7 mm of the optic apparatus (optic nerves, chiasm and optic tracts). iii. Diagnosis of leptomeningeal disease. iv. Prior SRS to an immediately adjacent lesion(s) of interest or to the current lesion(s) of interest. v. Prior history of pseudoprogression or radionecrosis from cranial radiotherapy. vi. A neurosurgical resection cavity deemed too large by the radiation oncologist to be treated with a single fraction of stereotactic radiosurgery. vii. Contraindications to gadolinium contrast-enhanced MRI (eg, non-compatible pacemaker, eGFR \<30, gadolinium allergy). viii. A Gustave Roussy Immune Score (GRIm-Score) \> 1 (neutrophil-to-lymphocyte ratio \> 6 = 1 point, LDH \> Upper Limit of Normal = 1 point, and Albumin \< 3.5 g/dL = 1 point).

Design outcomes

Primary

MeasureTime frameDescription
Multi-Fraction SRS superiority compared to single fraction SRS4 yearsTo determine if Multi-Fraction SRS will decrease the rate of radionecrosis when compared to single-fraction SRS for patients with small metastases and are on immunotherapy.

Secondary

MeasureTime frameDescription
Overall Survival Rate4 yearsTime from randomization to death
Acute CTCAE v5.0 CNS Grade 2+ and Grade 3+ toxicities4 yearsAny acute CTCAE v5.0 CNS Grade 2+ and Grade 3+ toxicities, within 90 days of SRS completion (toxicity must be specified).
Late CTCAE v5.0 CNS Grade 2+ and Grade 3+ toxicities4 yearsAny late CTCAE v5.0 CNS Grade 2+ and Grade 3+ toxicities, greater than 90 days from SRS completion (toxicity must be specified).
rate of individual metastases radionecrosis4 yearsTo compare the rates over time of individual metastases radionecrosis using a parametric survival analysis
Target metastasis progression4 yearsTarget metastasis progression will be assessed using adapted Response Assessment in Neuro-Oncology Brain Metastases (RANO-BM) consensus imaging criteria. In brief, progressive disease is defined as a ≥20% relative increase in the longest diameter (LD) of the target metastasis compared to its smallest LD recorded on study, with a minimum absolute increase of 5 mm
Rates of Symptomatic Edema1 yearTo compare rates of symptomatic edema at 3 months, 6 months, and 1 year.1
Time to any distant intracranial failure4 yearsTime to any distant intracranial failure (ie, appearance of brain metastasis at untreated site).
Time to initiation of any combination4 yearsTime to initiation of any combination of death, salvage SRS, WBRT, or neurosurgical resection for intracranial failure.
rate of individual metastases rates of edema4 yearsTo compare rates over time of individual metastases rates of edema using a parametric survival analysis.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026