Phase I/II Study To Test The Safety and Efficacy of TVI-Brain-1 As A Treatment For Recurrent Grade IV Glioma
| Status: | Completed |
|---|---|
| Conditions: | Brain Cancer, Brain Cancer |
| Therapuetic Areas: | Oncology |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 10/14/2017 |
| Start Date: | April 2010 |
| End Date: | March 2011 |
TVI-Brain-1 is an experimental treatment that takes advantage of the fact that your body can
produce immune cells, called 'killer' white blood cells that have the ability to kill large
numbers of the cancer cells that are present in your body. TVI-Brain-1 is designed to
generate large numbers of those 'killer' white blood cells and to deliver those cells into
your body so that they can kill your cancer cells.
produce immune cells, called 'killer' white blood cells that have the ability to kill large
numbers of the cancer cells that are present in your body. TVI-Brain-1 is designed to
generate large numbers of those 'killer' white blood cells and to deliver those cells into
your body so that they can kill your cancer cells.
TVI-Brain-1 involves several steps. First, the patient's cancer will be surgically removed to
provide cells for the vaccine. Second, the patient will be vaccinated twice with those cells
and GM-CSF. Third, the patient's blood will be filtered for white cells which will then be
cultured and stimulated to reach a higher (killer) activity level. Fourth, the activated
white blood cells will be infused into the patient's bloodstream so that they will be able to
attack the cancer. Finally, the entire process starting with vaccination will be repeated,
for a total of two rounds of therapy.
provide cells for the vaccine. Second, the patient will be vaccinated twice with those cells
and GM-CSF. Third, the patient's blood will be filtered for white cells which will then be
cultured and stimulated to reach a higher (killer) activity level. Fourth, the activated
white blood cells will be infused into the patient's bloodstream so that they will be able to
attack the cancer. Finally, the entire process starting with vaccination will be repeated,
for a total of two rounds of therapy.
Inclusion Criteria:
- Age > 18
- Informed consent
- Diagnosis of grade IV glioma with progression following standard treatment.
- Must be able to tolerate surgery to provide tumor tissue for vaccine.
- Must be able to produce viable vaccine from tumor tissue.
- Eastern Cooperative Oncology Group (ECOG) performance status must be < 2 or Karnofsky
Performance Status must be 70 or greater.
- Negative HIV test.
- Negative for hepatitis B and C virus.
- Respiratory reserve must be reasonable.
- Sufficient renal function.
- Satisfactory blood counts.
- Negative pregnancy test for women of childbearing potential.
Exclusion Criteria:
- Surgically removed cancer reveals that it is not grade IV glioma.
- Concomitant life-threatening disease.
- Active autoimmune disease.
- Currently receiving chemotherapy or biological therapy for the treatment of cancer.
- Currently receiving immunosuppressive drugs for any reason.
- Prior treatment with Avastin or other anti-angiogenesis treatment within 6 months.
- Prior treatment with Gliadel wafers.
- Corticosteroids beyond peri-operative period.
- Psychological, familial, sociological or geographical conditions that do not permit
adequate medical follow-up and compliance with the study protocol.
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