3rd Generation GD-2 Chimeric Antigen Receptor and iCaspase Suicide Safety Switch, Neuroblastoma, GRAIN



Status:Active, not recruiting
Conditions:Brain Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:Any
Updated:4/17/2018
Start Date:August 2013
End Date:October 2030

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AUTOLOGOUS ACTIVATED T-CELLS TRANSDUCED WITH A 3rd GENERATION GD-2 CHIMERIC ANTIGEN RECEPTOR AND iCASPASE9 SAFETY SWITCH ADMINISTERED TO PATIENTS WITH RELAPSED OR REFRACTORY NEUROBLASTOMA (GRAIN)

Subjects that have relapsed or refractory neuroblastoma are invited to take part in this gene
transfer research study.

We have found from previous research that we can put a new gene called a chimeric antigen
receptor (CAR) into T cells that will make them recognize neuroblastoma cells and kill them.
In a previous clinical trial, we used a CAR that recognizes GD2, a protein found on almost
all neuroblastoma cells (GD2-CAR). We put this gene into T cells and gave them back to
patients that had neuroblastoma. The infusions were safe and in patients with disease at the
time of their infusion, the time to progression was longer if we could find GD2 T cells in
their blood for more than 6 weeks. Because of this, we think that if T cells are able to last
longer, they may have a better chance of killing neuroblastoma tumor cells.

Therefore, in this study we will add new genes to the GD2 T cells that can cause the cells to
live longer. These new genes are called CD28 and OX40. The purpose of this study will be to
determine the highest dose of iC9-GD2-CD28-OX40 (iC9-GD2) T cells that can safely be given to
patients with relapsed/refractory neuroblastoma.

In other clinical studies using T cells, some investigators found that giving chemotherapy
before the T cell infusion can improve the amount of time the T cells stay in the body and
therefore the effect the T cells can have. This is called lymphodepletion and we think that
it will allow the T cells we infuse to expand and stay longer in the body, and potentially
kill cancer cells more effectively.

The chemotherapy we will use for lymphodepletion is a combination of cyclophosphamide and
fludarabine.

Additionally, to effectively kill the tumor cells, it is important that the T cells are able
to survive and expand in the tumor. Recent studies have shown that solid tumors release a
substance (PD1) that can inhibit T cells after they arrive into the tumor tissue. In an
attempt to overcome the effect of PD1 in neuroblastoma we will also give a medication called
pembrolizumab.

We will make iC9-GD2 T cells by infecting normal T cells with a retroviral vector containing
the iC9-GD2 gene. After the new gene has been put into the T cells, the cells will be tested
to make sure that they kill GD2-positive neuroblastoma cells and then will be either given
fresh or frozen until the patient is ready for their infusion.

First, patients will receive cyclophosphamide and fludarabine intravenously (through a needle
inserted into a vein or your port-a-cath) for 2 days and then fludarabine alone for one day
(Day -4, -3,-2). On the next day (Day -1) patients will receive the drug called pembrolizumab
intravenously. Finally on Day 0 patients will be given an infusion of iC9 GD2 T cells into
the vein through an IV line at the assigned dose.

The iC9-GD2 T cell infusion will be given by the Center for Cell and Gene Therapy at Texas
Children's Hospital or Houston Methodist Hospital. The infusion will take between 5 and 10
minutes. Patients may need to stay in Houston for up to 4 weeks after the infusion so we can
monitor them for side effects.

On Day 21 (at the time of the week 3 visit), if the treatment was well tolerated, patients
will receive another dose of pembrolizumab intravenously.

There will be follow-up visits every 1-2 weeks during the first 2 months and then they will
be spaced out over a total of 15 years. Because the cells are modified with a new gene we
must follow patients for at least 15 years to see if there are any long term side effects of
gene transfer. During the visits, we will see how the patients are doing and during certain
time points we will obtain extra blood samples to learn more about the way the iC9-GD2 T
cells are working and how long they last in the body.

After disease re-evaluation, if disease has not gotten worse, or if in the future it seems
that patient might benefit and they have not had a severe side effect caused by the infusion
of their iC9-GD2 T cells, patients may be eligible to receive up to 2 additional doses of
their T cells. Each dose will be at the same dose level as their first infusion and separated
by at least 6 weeks such that we can make sure patients have no severe side effects between
infusions. If patients receive additional doses of iC9-GD2 T-cells, they may need to stay in
Houston for up to 4 weeks after the infusion as well so we can monitor them for side effects.
If there were no severe side effects from pembrolizumab, patients will receive pembrolizumab
again with the iC9 GD2 T cells on the day before the T cell injection and 21 days after the T
cells.

Inclusion Criteria:

PROCUREMENT

- High risk neuroblastoma with persistent or relapsed disease

- Life expectancy of at least 12 weeks

- Karnofsky/Lansky score of 60% or greater

- Absence of HAMA prior to enrollment (only in patients that have been previously
treated with murine antibodies)

- Informed consent and assent (as applicable) obtained from parent/guardian and child

TREATMENT:

- High risk neuroblastoma with persistent or relapsed disease

- Life expectancy of at least 12 weeks

- Karnofsky/Lansky score of 60% or greater

- Patients must have an ANC greater than or equal to 500, platelet count greater than or
equal to 20,000

- Pulse Ox greater than or equal to 90% on room air

- AST and ALT less than 5 times the upper limit of normal

- Total bilirubin less than 3 times the upper limit of normal

- Serum creatinine less than 3 times upper limit of normal. Creatinine clearance is
needed for patients with creatinine greater than 1.5 times upper limit of normal

- TSH normal for age. Patients using thyroid medication to facilitate a euthyroid state
must be on a stable dose for at least 1 month prior to planned infusion

- Recovered from acute effects of all prior chemotherapy. If some effects of therapy
have become chronic (i.e., treatment associated thrombocytopenia), the patient must be
clinically stable and meet all other eligibility criteria

- Absence of human anti-mouse antibodies (HAMA) prior to enrollment for patients who
have received prior therapy with murine antibodies

- Patients must have autologous transduced activated T-cells with greater than or equal
to 20% expression of GD2

- Pembrolizumab available for infusion

- Informed consent and assent (as applicable) obtained from parent/guardian and child

Exclusion Criteria:

PROCUREMENT:

- Rapidly progressive disease

- History of hypersensitivity to murine protein containing products

TREATMENT:

- Rapidly progressive disease

- Currently receiving other investigational drugs

- History of hypersensitivity to murine protein containing products

- History of cardiomegaly or bilateral pulmonary infiltrates on chest radiograph or CT.
However, patients with cardiomegaly on imaging may be enrolled if they have an
assessment of cardiac function (i.e., ECHO or MUGA) within 3 weeks of starting
protocol therapy that is within normal limits. Additionally, patients with bilateral
pulmonary infiltrates on imaging may be enrolled if the lesions are not consistent
with active neuroblastoma (i.e., negative on functional imaging with PET or MIBG, or
by pathologic assessment).

- Evidence of tumor potentially causing airway obstruction

- Patients who are pregnant, lactating, or unwilling to use birth control

- Patients currently receiving immunosuppressive drugs such as corticosteroids,
tacrolimus or cyclosporine

- Patients previously experienced severe toxicity from cyclophosphamide or fludarabine

- Severe previous toxicity from pembrolizumab or other PD-1 targeted antibody
We found this trial at
2
sites
6550 Fannin St
Houston, Texas 77030
(713) 790-3311
Houston Methodist Hospital Houston Methodist is comprised of a leading academic medical center in the...
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6621 Fannin St
Houston, Texas 77030
(832) 824-1000
Texas Children's Hospital Texas Children's Hospital, located in Houston, Texas, is a not-for-profit organization whose...
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Houston, TX
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