Mode
Text Size
Log in / Sign up
Phase 1 N=16 Treatment

Genetically Modified Neural Stem Cells, Flucytosine, and Leucovorin for Treating Patients With Recurrent High-Grade Gliomas

Adult Anaplastic Astrocytoma · Adult Anaplastic Oligodendroglioma · Adult Giant Cell Glioblastoma · Adult Glioblastoma · Adult Gliosarcoma

Enrolled (actual)
16
Serious AEs
50.0%
Results posted
Sep 2021
Primary outcome: Primary: Number of Participants With Dose Limiting Toxicities (DLTs) and Maximum Tolerated Dose (MTD) — 0; 0; 0; 1 Participants

Study Design & Population

Study type
Interventional
Phase
Phase 1
Interventions
E. coli CD-expressing genetically modified neural stem cells (Biological); flucytosine (Drug); leucovorin calcium (Drug); pharmacological study (Other); laboratory biomarker analysis (Other)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
City of Hope Medical Center
Primary completion
Oct 2017

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants With Dose Limiting Toxicities (DLTs) and Maximum Tolerated Dose (MTD)
0; 0; 0; 1
PRIMARY
Number of Participants With Mechanical Issues With Repeat Administrations of NSCs Via Rickham
0; 0; 0; 0
SECONDARY
Number of Participants Developing Antibodies Against NSCs
0; 2; 0; 1
SECONDARY
Average Steady State Levels of 5-FC and 5-FU in the Brain
213; 0.03
SECONDARY
Average Steady State Levels of 5-FC Concentrations in Plasma
748
SECONDARY
Comparison of 5-FC in the Brain to 5-FC in the Plasma
29
SECONDARY
Summary of Tumor Response Using the Response Assessment in Neuro-Oncology (RANO) Criteria
2; 0; 0; 1; 1; 3

Summary

This phase I trial studies the side effects and determines the best dose of genetically modified neural stem cells and flucytosine when given together with leucovorin for treating patients with recurrent high-grade gliomas. Neural stem cells can travel to sites of tumor in the brain. The neural stem cells that are being used in this study were genetically modified express the enzyme cytosine deaminase (CD), which converts the prodrug flucytosine (5-FC) into the chemotherapy agent 5-fluorouracil (5-FU). Leucovorin may help 5-FU kill more tumor cells. The CD-expressing neural stem cells are administered directly into the brain. After giving the neural stem cells a few days to spread out and migrate to tumor cells, research participants take a 7 day course of oral 5-FC. (Depending on when a research participant enters the study, they may also be given leucovorin to take with the 5-FC.) When the 5-FC crosses into brain, the neural stem cells convert it into 5-FU, which diffuses out of the neural stem cells to preferentially kill rapidly dividing tumor cells while minimizing toxicity to healthy tissues. A Rickham catheter, placed at the time of surgery, will be used to administer additional doses of NSCs every two weeks, followed each time by a 7 day course of oral 5-FC (and possibly leucovorin). This neural stem cell-based anti-cancer strategy may be an effective treatment for high-grade gliomas. Funding Source - FDA OOPD

Eligibility Criteria

Inclusion Criteria

  • Patient has had a prior, histologically-confirmed, diagnosis of a grade III or IV glioma (including glioblastoma, anaplastic oligodendroglioma, or anaplastic astrocytoma, gliosarcoma, anaplastic oligodendroglioma, or anaplastic oligoastrocytoma), or has a prior, histologically-confirmed, diagnosis of a grade II glioma and now has radiographic findings consistent with a high-grade glioma (grade III or IV)
  • Imaging studies show evidence of recurrent, supratentorial tumor(s). The presence of infratentorial tumor is allowed as long as the patient also has supratentorial disease that is amenable to resection or biopsy.
  • Patient's high-grade glioma has recurred or progressed after prior treatment with brain radiation and temozolomide
  • Patient has a Karnofsky performance status of >= 70%
  • Patient has a life expectancy of >= 3 months
  • Female patients of childbearing potential and sexually-active male patients must agree to use an effective method of contraception while participating in this study; women of childbearing potential must have a negative pregnancy test = = 1500 cells/mm^3
  • Platelet count >= 100,000 cells/mm^3
  • Total bilirubin =< 2.0 mg/dl
  • Aspartate aminotransferase (AST) (serum glutamic oxaloacetic transaminase [SGOT]) =< 4 times the institutional upper limit of normal
  • Serum creatinine =< the institutional upper limit of normal
  • There is no limit to the number of prior therapies
  • All subjects must have the ability to understand and the willingness to sign a written informed consent

Exclusion Criteria

  • Patient has anti-human leukocyte antigen (HLA) antibodies specific for HLA antigens expressed by the NSCs
  • Patient has not recovered from any toxicity of prior therapies; an interval of
  • At least 6 weeks must have elapsed since taking a nitrosourea-containing chemotherapy regimen
  • At least 4 weeks since completing a non-nitrosourea-containing cytotoxic chemotherapy regimen (except temozolomide: only an interval of 23 days is required from the last dose administered when patient has been recently treated with the standard temozolomide regimen of daily for 5 days, repeated every 28 days)
  • At least 2 weeks from taking the last dose of targeted agent
  • At least 4 weeks from the last dose of bevacizumab
  • Patient is unable to undergo a magnetic resonance imaging (MRI)
  • Patient is allergic to 5-FC, leucovorin, or 5-FU
  • Patient has chronic or active viral infections of the central nervous system (CNS)
  • Patient has a coagulopathy or bleeding disorder
  • Patient has an uncontrolled illness including ongoing or active infection
  • Patient is receiving any other investigational agents, or concurrent biological, chemotherapy, or radiation therapy
  • Patient has had prior therapy with neural stem cells
  • Patient is pregnant or breast feeding; pregnant women are excluded from this study; breastfeeding should be discontinued if the mother is participating in this study
  • Patient has another active malignancy
  • Non-compliance; a patient has a serious medical or psychiatric illness that could, in the investigator's opinion, potentially interfere with the safety monitoring requirements and completion of treatment according to this protocol
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02015819). 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.

Back to search