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NCT Number: NCT05128903

Quantitative Assessment of Radiation-induced Neuroinflammation - A Proof of Principle Study

QARIN 1 is a study of [18F]DPA-714 Translocation Protein (TSPO) Positron Emission Tomography (PET) for longitudinal, quantitative assessment of brain neuroinflammation following whole brain radiation therapy. This TSPO PET, uses a radioactive tracer. An optional MRI (magnetic resonance imaging) will also be performed to monitor brain microstructure damages induced by neuroinflammation.

Primary Objectives

* Assessment of temporal and regional variability of uptake of translocator protein (TSPO) positron emission tomography (PET) tracer. * Regional variability will be assessed in medial temporal lobe, frontal lobe, and in white matter * Temporal variability will be assessed by scanning each subject four-times: at baseline (before or within 2 weeks of start of radiation therapy), before start of chemotherapy, at 1 year from the initiation of the radiation therapy, and at 1.5-2 years from the initiation of the radiation therapy * Correlation of radiation dose in specific brain regions with radiation induced neuroinflammation as measured by uptake of TSPO PET tracer.

Exploratory Objectives

* Assessment of radiation-induced brain microstructure injuries (RIBMI) in specific brain regions (medial temporal lobe, frontal lobe, and in white matter) using advanced magnetic resonance imaging (MRI) techniques. * Association of radiation dose with MRI measures of RIBMI in these specific brain regions. * Association of PET measures of RIN with MRI measures of RIBMI. * Association of PET measure of RIN and MRI measures of RIBMI in specific regions of interest (ROI) with specific domain of neuro-cognition. For example, to investigate whether PET measure of RIN and MRI measures of RIBMI in hippocampal ROI have strongest association with episodic memory; whether frontal lobe cortical ROI are associated with attention and executive function. * Association of a novel MRI based technique for assessment of RIN with TSPO PET. * Association of the PET and MRI measure of neuroinflammation within 2- years of completion of radiation with delayed cognitive outcome that will be measured at 3, 4 and 5 years from the completion of radiation

Active, Not Recruiting

This study is active but is not currently recruiting participants.

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Key information

Conditions

Brain Tumor Brain Diseases Brain Neoplasms Central Nervous System Diseases Central Nervous System Neoplasms Glioma Medulloblastoma Neoplasms Neoplasms by Histologic Type Neoplasms by Site Neoplasms, Germ Cell and Embryonal Neoplasms, Glandular and Epithelial Neoplasms, Nerve Tissue Neoplasms, Neuroepithelial Nervous System Diseases Nervous System Neoplasms Neuroectodermal Tumors Neuroectodermal Tumors, Primitive

Age range

8 year–39 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

St.Jude Children's Research Hospital

Memphis, Tennessee, 38105, United States

About this study

The participant will have 4 PET scans using a novel PET tracer that will help the investigators to quantify when and where in brain neuroinflammation happens following radiation therapy. The participant will receive the first PET scan either before your first dose of radiation therapy or within 2 weeks of the start of radiation therapy. The second PET scan will be obtained before starting chemotherapy. The third scan will be after 1 year of treatment.The final scan will be 1 and a half to 2 years after the start of treatment.The scan process will begin an hour or so after the participant has been given tracer by injection. The entire PET scan process lasts about 2 hours.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Participant is at least 8 years of age
  • Participants with histologically confirmed medulloblastoma and are scheduled to receive 36 Gy craniospinal irradiation
  • Participant and/or guardian can understand and is willing to sign a written informed consent document according to institutional guidelines
  • Subjects have either have high-affinity or mixed-affinity TSPO binding sites as determined by the single-nucleotide polymorphism (SNP) rs6971 in the TSPO gene.

Exclusion criteria

  • Participants with a large pseudomeningocele (>4 cm in size) at the surgical site, complications from ventricular access (evidenced by hemorrhage and/or enhancement along the catheter), large subdural effusion in the supra-tentorial compartment (>1 cm in the maximum transverse dimension). All of these are expected to induce inflammation.
  • Female participants of childbearing age must not be lactating due to theoretical potential harm to the infant from exposure to radiation.
  • Subjects with low-affinity TSPO binding sites as determined by the single-nucleotide polymorphism (SNP) rs6971 in the TSPO gene.
  • Pregnant subjects.
  • Patients needing sedation for the PET scans or optional MRI scans.
  • Participants with a diagnosis of recurrent medulloblastoma.

Treatment and study plan

[18F]DPA714

Drug

Intravenous injection

  • Before or within 2 weeks of starting radiation therapy
  • Before starting chemotherapy
  • 1 year after the start of radiation therapy Timing cont.
  • 1.5 to 2 years after the start of radiation therapy

Primary outcomes

  1. SUVr

    Time frame: follow up 1: up to 13 weeks after radiation therapy

    SUVr values for dorsolateral prefrontal cortex comparing baseline vs. follow up 1

  2. SUVr

    Time frame: follow up 1 : up to 13 weeks after radiation therapy

    SUVr values for medial prefrontal cortex comparing baseline vs. follow up 1

  3. SUVr

    Time frame: follow up 1 : up to 13 weeks after radiation therapy

    SUVr values for hippocampus comparing baseline vs. follow up 1.

  4. SUVr

    Time frame: follow up 1 : up to 13 weeks after radiation therapy

    SUVr values for Corpus callosum comparing baseline vs. follow up 1.

  5. SUVr

    Time frame: follow up 1 : up to 13 weeks after radiation therapy

    SUVr values for corticospinal tract comparing baseline vs. follow up 1.

  6. SUVr

    Time frame: follow up 1 : up to 13 weeks after radiation therapy

    SUVr values for superior longitudinal fasciculus comparing baseline vs. follow up 1

  7. SUVr

    Time frame: follow up 2: up to 53 weeks after radiation therapy

    SUVr values for dorsolateral prefrontal cortex comparing baseline vs. follow up 2.

  8. SUVr

    Time frame: follow up 2: up to 53 weeks after radiation therapy

    SUVr values for medial prefrontal cortex comparing baseline vs. follow up 2.

  9. SUVr

    Time frame: follow up 2: up to 53 weeks after radiation therapy

    SUVr values for hippocampus comparing baseline vs. follow up 2.

  10. SUVr

    Time frame: follow up 2: up to 53 weeks after radiation therapy

    SUVr values for Corpus callosum comparing baseline vs. follow up 2.

  11. SUVr

    Time frame: follow up 2: up to 53 weeks after radiation therapy

    SUVr values for corticospinal tract comparing baseline vs. follow up 2.

  12. SUVr

    Time frame: follow up 2: up to 53 weeks after radiation therapy

    SUVr values for superior longitudinal fasciculus comparing baseline vs. follow up 2.

  13. SUVr

    Time frame: follow up 3: up to 2 years after radiation therapy

    SUVr values for dorsolateral prefrontal cortex comparing baseline vs. follow up 3.

  14. SUVr

    Time frame: follow up 3: up to 2 years after radiation therapy

    SUVr values for medial prefrontal cortex comparing baseline vs. follow up 3.

  15. SUVr

    Time frame: follow up 3: up to 2 years after radiation therapy

    SUVr values for hippocampus comparing baseline vs. follow up 3.

  16. SUVr

    Time frame: follow up 3: up to 2 years after radiation therapy

    SUVr values for Corpus callosum comparing baseline vs. follow up 3

  17. SUVr

    Time frame: follow up 3: up to 2 years after radiation therapy

    SUVr values for corticospinal tract comparing baseline vs. follow up 3.

  18. SUVr

    Time frame: follow up 3: up to 2 years after radiation therapy

    SUVr values for superior longitudinal fasciculus comparing baseline vs. follow up 3.

Sponsors and collaborators

Lead sponsor

St. Jude Children's Research Hospital

Other

Registry information

Important dates

Study start
2022
Primary completion
2035
Study completion
2035
First posted
Nov 22, 2021
Registry last updated
Apr 24, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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