Radiogenomic and Prognosis Analysis in Glioma

Sponsor
Asan Medical Center (Other)
Overall Status
Unknown status
CT.gov ID
NCT04122521
Collaborator
(none)
62
1
12.7
4.9

Study Details

Study Description

Brief Summary

This study aims to evaluate whether MRI can be used to predict genomics and prognosis in glioma. Given the profound prognostic significance of genetic mutations seen in glioma, there have been increasing attempts to correlate imaging characteristics with genetic, mutational and expression patterns. To be able to predict genomics and prognosis based on imaging alone will prove useful in patients with involvement of glioma in delicate areas of the brain and better reflect tumor and molecular heterogeneity.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: MRI

Detailed Description

Previous studies have proposed certain imaging characteristics correlating with genetic, molecular and expression patterns. Advanced imaging provides additional clues but no studies have examined its added value particularly in a prospective setting. The investigator's aim to evaluate preoperative MRI for patients suspected of glioma to predict IDH mutation, 1p19q codeletion, MGMT methylation and EGFR mutation status using imaging characteristics such as margin, patterns of contrast enhancement and edema as well as diffusion and perfusion characteristics. This will be confirmed pathologically and further correlated with patients' long term outcome.

Study Design

Study Type:
Observational
Anticipated Enrollment :
62 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Prospective Observational Study of Imaging-based Prediction for Genomic Mutations and Prognosis in Glioma
Actual Study Start Date :
Jan 12, 2020
Anticipated Primary Completion Date :
Feb 1, 2021
Anticipated Study Completion Date :
Feb 1, 2021

Arms and Interventions

Arm Intervention/Treatment
Glioma

Patients suspected of glioma

Diagnostic Test: MRI
MRI

Outcome Measures

Primary Outcome Measures

  1. Time to progression [Through study completion, an average of 2 years]

    The response was determined by a modification of the response assessment in neuro-oncology (RANO) criteria that combined the image assessment, neurologic evaluation and assessment of steroid use.

Secondary Outcome Measures

  1. Genomics including IDH mutation, 1p19q codeletion, MGMT methylation and EGFR mutation status [2 months]

    Proportion of positive IDH mutation, 1p19q codeletion, MGMT methylation and EGFR mutation in percentage (%)

  2. Progression free survival [Through study completion, an average of 3 years]

    Estimated probable duration of life without disease progression, from on-study date to earlier progression date or date of death from any cause, using the Kaplan-Meier method with censoring. The response was determined by a modification of the RANO criteria that combined the image assessment, neurologic evaluation and assessment of steroid use.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Inclusion Criteria:
  • Patients suspected of glioma undergoing MRI examination prior to surgery

  • MRI including advanced imaging such as cerebral blood volume, apparent diffusion coefficient and amide proton transfer imaging

  • Signed informed consent

Exclusion Criteria:
  • Pathologic confirmation as tumors other than glioma

  • Patients who have any type of bioimplant activated by mechanical, electronic, or magnetic means (e.g., cochlear implants, pacemakers, neurostimulators, biostimulates, electronic infusion pumps, etc), because such devices may be displaced or malfunction

  • Patients who are pregnant or breast feeding; urine pregnancy test will be performed on women of child bearing potential

Contacts and Locations

Locations

Site City State Country Postal Code
1 Asan Medical Center Seoul Korea, Republic of

Sponsors and Collaborators

  • Asan Medical Center

Investigators

  • Principal Investigator: Ho Sung Kim, MD PhD, Asan Medical Center
  • Study Director: Ji Eun Park, MD PhD, Asan Medical Center

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ho Sung Kim, Professor, Asan Medical Center
ClinicalTrials.gov Identifier:
NCT04122521
Other Study ID Numbers:
  • AsanMCHSKim_03
First Posted:
Oct 10, 2019
Last Update Posted:
Feb 7, 2020
Last Verified:
Feb 1, 2020
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 7, 2020