Clinical trial · Interventional
O6-Benzylguanine-Mediated Tumor Sensitization With Chemoprotected Autologous Stem Cell in Treating Patients With Malignant Gliomas
Benzylguanine-Mediated Tumor Sensitization With Chemoprotected Autologous Stem Cells for Patients With Malignant Gliomas
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): Terminated due to loss in funding.
Summary
Brief summary (as posted)
This phase I/II trial studies the side effects and best dose of temozolomide when given together with radiation therapy, carmustine, O6-benzylguanine, and patients' own stem cell (autologous) transplant in treating patients with newly diagnosed glioblastoma multiforme or gliosarcoma. Giving chemotherapy, such as temozolomide, carmustine, and O6-benzylguanine, and radiation therapy before a peripheral stem cell transplant stops the growth of cancer cells by stopping them from dividing or killing them. Giving colony-stimulating factors, such as filgrastim or plerixafor, and certain chemotherapy drugs, helps stem cells move from the bone marrow to the blood so they can be collected and stored. Chemotherapy or radiation therapy is then given to prepare the bone marrow for the stem cell transplant. The stem cells are then returned to the patient to replace the blood-forming cells that were destroyed by the chemotherapy and radiation therapy.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Glioblastoma | Glioblastoma | CURATED_BROADER | 0.80 |
| Gliosarcoma | Gliosarcoma | ONTOLOGY_EXACT | 0.90 |
Interventions
Interventions (11)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| 3-Dimensional Conformal Radiation Therapy | Radiation | — | UNRESOLVED |
| Autologous Hematopoietic Stem Cell Transplantation | Procedure | — | UNRESOLVED |
| Carmustine | Drug | Carmustine | ALIAS |
| Filgrastim | Biological | Filgrastim | ALIAS |
| Intensity-Modulated Radiation Therapy | Radiation | — | UNRESOLVED |
| In Vitro-Treated Peripheral Blood Stem Cell Transplantation | Procedure | — | UNRESOLVED |
| Laboratory Biomarker Analysis | Other | — | UNRESOLVED |
| O6-Benzylguanine | Drug | O6-Benzylguanine |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Treatment (chemotherapy, autologous stem cell transplant)
- description
- See Detailed Description
- interventionNames
- Radiation: 3-Dimensional Conformal Radiation Therapy
- Procedure: Autologous Hematopoietic Stem Cell Transplantation
- Drug: Carmustine
- Biological: Filgrastim
- Procedure: In Vitro-Treated Peripheral Blood Stem Cell Transplantation
- Radiation: Intensity-Modulated Radiation Therapy
- Other: Laboratory Biomarker Analysis
- Drug: O6-Benzylguanine
- Drug: Plerixafor
- Radiation: Proton Beam Radiation Therapy
- Drug: Temozolomide
Primary outcomes (2)
- measure
- Number of Participants Dose-limiting Toxicity (DLT)
- timeFrame
- Up to 6 weeks after infusion
- description
- Defined as any grade 4 nonhematopoietic toxicity that is likely related to the investigational procedures (Part I)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Patients with glioblastoma multiforme or gliosarcoma * The patient or legal guardian must be able to comprehend the informed consent form and sign prior to patient enrollment * Karnofsky performance status at time of study entry must be \>= 70% * Life expectancy of \>= 3 months * Patients must agree to undergo repeat clinical neurological examinations and brain magnetic resonance imaging (MRI) with appropriate contrast after every other cycle of chemotherapy * White blood cell (WBC) \> 3000/ul * Absolute neutrophil count (ANC) \> 1500/ul * Platelets \> 100,000/ul * Hemoglobin \> 10 gm/100ml * Total and direct bilirubin \< 1.5 times upper limit of laboratory normal * Serum glutamic oxaloacetic transaminase (SGOT) and serum glutamate pyruvate transaminase (SGPT) =\< 3 times upper limit of laboratory normal * Alkaline phosphatase =\< 3 times upper limit of laboratory normal * Blood urea nitrogen (BUN) \< 1.5 times upper limit of laboratory normal * Serum creatinine \< 1.5 times upper limit of laboratory normal * Left ventricular ejection fraction (LVEF) \>= 40%, however, subjects with a LVEF in the range of 40-49% should have cardiology clearance prior to intervention * MGMT promoter methylation analysis of surgically resected tumor or tumor biopsy must demonstrate an unmethylated or hypomethylated MGMT promoter status Exclusion Criteria: * Patients with cardiac insufficiency and a LVEF of \< 40%; history of coronary artery disease or arrhythmia, which has required or requires ongoing treatment * Patients with active pulmonary infection and/or pulse oximetry \< 90% and a corrected diffusion capacity of the lung for carbon monoxide (DLCO) \< 70% of predicted * Active systemic infection * Patients who are human immunodeficiency virus (HIV) positive * Pregnant or lactating women; a beta-human chorionic gonadotropin (HCG) level will be obtained from women of childbearing potential; fertile men and women should use effective contraception * Previous chemotherapy for any malignancy including temozolomide, dacarbazine (DTIC) or prior nitrosourea * Diabetes mellitus * Bleeding disorder * Methylated or hypermethylated MGMT promoter status within tumor tissue * Medical or psychiatric condition which in the opinion of the protocol chairman would compromise the patient's ability to tolerate this protocol * Prior interstitial radiotherapy, stereotactic or gamma knife surgery or implanted BCNU-wafers
References
Publications (1)
- DERIVEDAdair JE, Johnston SK, Mrugala MM, Beard BC, Guyman LA, Baldock AL, Bridge CA, Hawkins-Daarud A, Gori JL, Born DE, Gonzalez-Cuyar LF, Silbergeld DL, Rockne RC, Storer BE, Rockhill JK, Swanson KR, Kiem HP. Gene therapy enhances chemotherapy tolerance and efficacy in glioblastoma patients. J Clin Invest. 2014 Sep;124(9):4082-92. doi: 10.1172/JCI76739. Epub 2014 Aug 8. PMID 25105369