Actively Recruiting
GD2 Specific CAR and Interleukin-15 Expressing Autologous NKT Cells to Treat Children With Neuroblastoma
Led by Baylor College of Medicine · Updated on 2025-09-19
70
Participants Needed
1
Research Sites
1177 weeks
Total Duration
On this page
Sponsors
B
Baylor College of Medicine
Lead Sponsor
C
Center for Cell and Gene Therapy, Baylor College of Medicine
Collaborating Sponsor
AI-Summary
What this Trial Is About
This research study combines two different ways of fighting cancer: antibodies and Natural Killer T cells (NKT). Antibodies are types of proteins that protect the body from infectious diseases and possibly cancer. T cells, also called T lymphocytes, are special white blood cells that can kill other cells, including cells infected with viruses and tumor cells. Both antibodies and T cells have been used to treat patients with cancers. Investigators have found from previous research that they can put a new gene into T cells that will make them recognize cancer cells and kill them. In a previous clinical trial, investigators made artificial genes called a chimeric antigen receptors (CAR), from an antibody called 14g2a that recognizes GD2, a molecule found on almost all neuroblastoma cells (GD2-CAR). Investigators put these genes into the patients' own T cells and gave them back to patients that had neuroblastoma. NKT cells are another special subgroup of white blood cells that can specifically go into tumor tissue of neuroblastoma. Inside the tumor, there are other white blood cells called macrophages which help the cancer cells to grow and recover from injury. NKT cells can specifically kill these macrophages and slow the tumor growth. We will expand NKT cells and add GD2-specific chimeric antigen receptors to the cells. We think these cells might be better able to attack NB since they also work by destroying the macrophages that allows the tumor to grow. The chimeric antigen receptor will also contain a gene segment to make the NKT cells last longer. This gene segment is called CD28. In addition, to further improve the antitumor activity of the GINAKIT cells we added another gene expressing a molecule called Interleukin -15 (IL-15). The combination of these 3 components showed the most antitumor activity by CAR expressing NKT cells and improved these cells' survival in animal models. We also found that a medicine called ETANercept can slow down neuroblastoma growth, which might enhance the effects of the modified cells. In this part of our study, we aim to treat children with hard-to-treat neuroblastoma using these modified NKT cells along with ETANercept. Though ETANercept has been used to treat other diseases, such as rheumatoid arthritis in children, there is limited information about the safety, efficacy, and risk of ETANercept treatment in combination with cellular therapies. GD2-CAR expressing NKTs have not been tested in patients so far. The purpose of this study is to find the largest effective and safe dose of GD2-CAR NKT cells (GINAKIT cells), to evaluate their effect on the tumor and how long they can be detected in the patient's blood and what affect they have on the patient's neuroblastoma.
CONDITIONS
Official Title
GD2 Specific CAR and Interleukin-15 Expressing Autologous NKT Cells to Treat Children With Neuroblastoma
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Relapsed or refractory high-risk neuroblastoma
- Life expectancy of at least 12 weeks
- Age greater than 1 year and less than 21 years old
- Karnofsky/Lansky score of 60% or greater
- Absence of human anti-mouse antibodies prior to enrollment (for those previously treated with murine antibodies)
- Ability to tolerate leukocyte apheresis
- Informed consent and assent obtained from parent/guardian and child as applicable
- Absolute neutrophil count (ANC) of at least 500/µl
- Platelet count of at least 20,000/µl (transfusions allowed to meet this)
- Pulse oximetry of 90% or greater on room air
- Serum AST less than 3 times the upper limit of normal
- Total bilirubin less than 1.5 times the upper limit of normal
- Creatinine less than 1.5 times the upper limit of normal
- Recovery from acute toxic effects of prior chemotherapy as assessed by physician
- Weight greater than 12 kg
- Negative tuberculosis test (QuantiFERON-TB or T-SPOT) within 3 months prior to procurement or treatment start
- For treatment, must have autologous transduced NKTs with at least 20% expression of GD2-specific CAR
You will not qualify if you...
- Rapidly progressive disease
- History or hypersensitivity to murine protein-containing products
- Tumor causing airway obstruction
- Currently receiving immunosuppressive drugs such as corticosteroids, tacrolimus, or cyclosporine
- Severe previous toxicity from cyclophosphamide or fludarabine as assessed by physician
- HIV infection
- History of hypersensitivity, anaphylaxis, or adverse event with Etanercept
- Currently receiving any investigational drugs (treatment exclusion)
- Cardiomegaly or bilateral pulmonary infiltrates on imaging unless cardiac function is normal and lesions are not active neuroblastoma
- Pregnancy or lactation or unwillingness to use birth control (treatment exclusion)
AI-Screening
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Trial Site Locations
Total: 1 location
1
Texas Children's Hospital
Houston, Texas, United States, 77030
Actively Recruiting
Research Team
G
Gengwen Tian, MD
CONTACT
R
Ramy Sweidan
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
2
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