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Phase 2 N=31 Treatment

Low Dose Radiation Therapy for Glioblastoma Multiforme

High Grade Glioma

Enrolled (actual)
31
Serious AEs
100.0%
Results posted
Jul 2023
Primary outcome: Primary: Response Rate

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Low Dose Fractionated Radiation Therapy (LDFRT) (Radiation); Temozolomide (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
Primary completion
Dec 2021

Outcome Measures

OutcomeResultp-value
PRIMARY
Response Rate
PRIMARY
Overall Survival Rate
9.6
SECONDARY
Progression Free Survival Rate
7.3
SECONDARY
Number of Patients With Hematologic Toxicities
8
SECONDARY
Number of Patients With Neurologic Toxicity
6

Summary

To evaluate the safety and effectiveness of low dose rate radiation therapy plus temozolomide. This will be in patients with High Grade Glioma (to only include Anaplastic Astrocytoma or Glioblastoma Multiforme) who have previously been treated with surgery followed by radiation surgical resection followed by adjuvant radiation therapy plus temozolomide.

Eligibility Criteria

Inclusion Criteria

  • Patients must have recurrent GBM (Glioblastoma Multiforme)or Anaplastic Astrocytoma.
  • The diagnosis of GBM or Anaplastic Astrocytoma.
  • Patients must have been previously treated with surgical resection (any extent okay) and adjuvant radiation therapy plus temozolomide.
  • Patients must be at least 12 months from completion of radiation therapy
  • At least 2 months from completion of temozolomide (to be consistent with the the "rechallenge" group from Perry et al. JCO 2010).
  • Age >18 years
  • ECOG performance status 60%, see appendix A).
  • There must be measurable disease on MRI.
  • Patients must have normal organ and marrow function as defined below:
  • Women must not be pregnant
  • Ability to understand and the willingness to sign a written informed consent document
  • Temozolomide re-treatment is planned by the treating neuro-oncologist.
  • The most recent brain tumor pathology obtained for the patient must be glioblastoma.

Exclusion Criteria

  • Must be able to receive an MRI
  • Patients may not be receiving any other investigational cancer treatment agents at the time of enrollment.
  • Patients may not have previously failed treatment with salvage temozolomide.
  • Patients may not have previously failed treatment with a VEGF inhibitor.
  • Patients may not have previously been treated with >1 course of radiotherapy.
  • Patients may not have previously been treated with radiosurgery to the brain.
  • Uncontrolled intercurrent illness
  • Pregnant and breastfeeding women are excluded. Women of child-bearing potential who are unwilling or unable to use and acceptable method of birth control to avoid pregnancy for the entire study period and up to 12 weeks after the study are excluded. Male subjects must also agree to use effective contraception for the same period as above.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01466686). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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