Kappa-CD28 T Lymphocytes, Chronic Lymphocytic Leukemia, B-cell Lymphoma or Multiple Myeloma, CHARKALL
| Status: | Recruiting |
|---|---|
| Conditions: | Blood Cancer, Lymphoma, Hematology, Hematology, Leukemia |
| Therapuetic Areas: | Hematology, Oncology |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 3/9/2019 |
| Start Date: | July 2009 |
| End Date: | July 2034 |
| Contact: | Carlos Ramos, MD |
| Email: | caramos@txch.org |
| Phone: | 832-824-4817 |
Phase I Study of Adoptive Transfer of Autologous T Lymphocytes Engrafted With a Chimeric Antigen Receptor Targeting the Kappa Light Chain of Immunoglobulin Expressed in Patients With CLL, B-Cell Lymphoma or Multiple Myeloma
Patients have a type of cancer called NHL, Multiple Myeloma (MM) or CLL that has come back or
has not gone away after treatment. There is no standard treatment for the cancer at this time
or the currently used treatments do not work completely in all cases like these. This is a
gene transfer research study using special immune cells.
The body has different ways of fighting infection and disease. No single way seems perfect
for fighting cancers. This research study combines two different ways of fighting disease,
antibodies and T cells, that investigators hope will work together. Antibodies are types of
proteins that protect the body from bacterial and other diseases. T cells, also called T
lymphocytes, are special infection-fighting blood cells that can kill other cells, including
tumor cells. Both antibodies and T cells have been used to treat patients with cancers; they
have shown promise, but have not been strong enough to cure most patients.
The antibody used in this study recognizes a protein on the lymphoma, MM or CLL cells called
kappa immunoglobulin. Antibodies can stick to lymphoma, MM or CLL cells when it recognizes
the kappa molecules present on the tumor cells. For this study, the kappa antibody has been
changed so that instead of floating free in the blood it is now joined to the T cells. When
an antibody is joined to a T cell in this way it is called a chimeric receptor. These
chimeric receptor-T cells seem to kill some of the tumor, but they don't last very long and
so their chances of fighting the cancer are limited.
In the laboratory, investigators found that T cells work better if they also add a protein
that stimulates T cells to grow called CD28. By joining the anti-kappa antibody to the T
cells and adding the CD28, the investigators expect to be able to make cells that will last
for a longer time in the body (because of the presence of the CD28). They are hoping this
will make the cells work better.
Previously, when patients enrolled on this study, they were assigned to one of three
different doses of the kappa-CD28 T cells. We found that all three dose levels are safe. Now,
the plan is to give patients the highest dose that we tested.
These chimeric T cells (kappa-CD28) are an investigational product not approved by the FDA.
has not gone away after treatment. There is no standard treatment for the cancer at this time
or the currently used treatments do not work completely in all cases like these. This is a
gene transfer research study using special immune cells.
The body has different ways of fighting infection and disease. No single way seems perfect
for fighting cancers. This research study combines two different ways of fighting disease,
antibodies and T cells, that investigators hope will work together. Antibodies are types of
proteins that protect the body from bacterial and other diseases. T cells, also called T
lymphocytes, are special infection-fighting blood cells that can kill other cells, including
tumor cells. Both antibodies and T cells have been used to treat patients with cancers; they
have shown promise, but have not been strong enough to cure most patients.
The antibody used in this study recognizes a protein on the lymphoma, MM or CLL cells called
kappa immunoglobulin. Antibodies can stick to lymphoma, MM or CLL cells when it recognizes
the kappa molecules present on the tumor cells. For this study, the kappa antibody has been
changed so that instead of floating free in the blood it is now joined to the T cells. When
an antibody is joined to a T cell in this way it is called a chimeric receptor. These
chimeric receptor-T cells seem to kill some of the tumor, but they don't last very long and
so their chances of fighting the cancer are limited.
In the laboratory, investigators found that T cells work better if they also add a protein
that stimulates T cells to grow called CD28. By joining the anti-kappa antibody to the T
cells and adding the CD28, the investigators expect to be able to make cells that will last
for a longer time in the body (because of the presence of the CD28). They are hoping this
will make the cells work better.
Previously, when patients enrolled on this study, they were assigned to one of three
different doses of the kappa-CD28 T cells. We found that all three dose levels are safe. Now,
the plan is to give patients the highest dose that we tested.
These chimeric T cells (kappa-CD28) are an investigational product not approved by the FDA.
To prepare the lymphoma, MM or CLL specific T cells investigators will take 240 ml (up to 16
tablespoonfuls)of blood from the patient. This would be drawn as 2 (two) separate blood
collections of 120 ml (up to 8 tablespoonfuls) of blood.
To get the kappa antibody (with CD28) to attach to the surface of the T cell, investigators
inserted the antibody gene into the T cell. This is done with a virus called a retrovirus
that has been made for this study and will carry the antibody gene into the T cell. This
virus also helps investigators find the T cells in the patient's blood after they're
injected. Because the patient has received cells with a new gene in them patients will be
followed for a total of 15 years to see if there are any long term side effects of gene
transfer.
Several studies suggest that the infused T cells need room to be able to grow and accomplish
their functions and that this may not happen if there are too many other T cells in
circulation. Because of that, if the level of circulating T cells is relatively high or the
patient has B-CLL, the patient may receive treatment with cyclophosphamide and fludarabine
(Cy and Flu) prior to the infusion of the T cells. This drug will decrease the numbers of the
patients own T cells before infusion of the kappa-CD28 T cells. Although investigators don't
expect any effect on the tumor with the dose that the patient will receive, this drug is part
of many regimens that are used to treat lymphoma, MM or CLL. If you are already receiving
chemotherapy, this may not be needed.
Patients will be given an injection of cells into the vein through an IV line. If s/he
receives Cy and Flu as stated above, the T cells will be given no sooner than 24 hours
afterwards. If the patient has recently received other chemotherapy, the T cells will be
given at least 24 hours after their last chemotherapy. The injection will take about 20
minutes. Investigators will follow the patient in the clinic after the injection. The
treatment will be given by the Center for Cell and Gene Therapy at Texas Children's Hospital
or Houston Methodist Hospital.
If after a 4-6 week evaluation period after the infusion, the patient seems to be
experiencing a benefit (confirmed by radiological studies, physical exam and/or symptoms),
the patient may be able to receive additional doses of the T cells if they wish. These
additional infusions would be at least 4-6 weeks apart and at the same dose level they
received the first time or a lower dose. If the patient's circulating T cells are relatively
high prior to any additional doses of T cells, they may receive Cy and Flu beforehand.
tablespoonfuls)of blood from the patient. This would be drawn as 2 (two) separate blood
collections of 120 ml (up to 8 tablespoonfuls) of blood.
To get the kappa antibody (with CD28) to attach to the surface of the T cell, investigators
inserted the antibody gene into the T cell. This is done with a virus called a retrovirus
that has been made for this study and will carry the antibody gene into the T cell. This
virus also helps investigators find the T cells in the patient's blood after they're
injected. Because the patient has received cells with a new gene in them patients will be
followed for a total of 15 years to see if there are any long term side effects of gene
transfer.
Several studies suggest that the infused T cells need room to be able to grow and accomplish
their functions and that this may not happen if there are too many other T cells in
circulation. Because of that, if the level of circulating T cells is relatively high or the
patient has B-CLL, the patient may receive treatment with cyclophosphamide and fludarabine
(Cy and Flu) prior to the infusion of the T cells. This drug will decrease the numbers of the
patients own T cells before infusion of the kappa-CD28 T cells. Although investigators don't
expect any effect on the tumor with the dose that the patient will receive, this drug is part
of many regimens that are used to treat lymphoma, MM or CLL. If you are already receiving
chemotherapy, this may not be needed.
Patients will be given an injection of cells into the vein through an IV line. If s/he
receives Cy and Flu as stated above, the T cells will be given no sooner than 24 hours
afterwards. If the patient has recently received other chemotherapy, the T cells will be
given at least 24 hours after their last chemotherapy. The injection will take about 20
minutes. Investigators will follow the patient in the clinic after the injection. The
treatment will be given by the Center for Cell and Gene Therapy at Texas Children's Hospital
or Houston Methodist Hospital.
If after a 4-6 week evaluation period after the infusion, the patient seems to be
experiencing a benefit (confirmed by radiological studies, physical exam and/or symptoms),
the patient may be able to receive additional doses of the T cells if they wish. These
additional infusions would be at least 4-6 weeks apart and at the same dose level they
received the first time or a lower dose. If the patient's circulating T cells are relatively
high prior to any additional doses of T cells, they may receive Cy and Flu beforehand.
INCLUSION CRITERIA:
BLOOD PROCUREMENT:
- B-CLL or recurrent or refractory B-cell lymphoma (or other B-cell neoplasm) and
Multiple Myeloma (MM) or multiple myeloma monoclonal for Kappa-light chain
- Life expectancy of at least 12 weeks or greater.
- No history of other cancer (except non-melanoma skin cancer or in situ breast cancer
or cervix cancer) unless the tumor was successfully treated with curative intent at
least 2 years before trial entry
- If requires pheresis to collect blood, Cre and AST less than 1.5 upper limit of normal
- If requires pheresis to collect blood, PT and PTTK less than 1.5 upper limit normal
T CELL TREATMENT:
Diagnosis of B-CLL monoclonal for Kappa light chain with one of the following criteria:
1. Evidence of progressive marrow failure as manifested by the development of, or
worsening of, anemia and/or thrombocytopenia
2. Massive (ie, at least 6 cm below the left costal margin) or progressive or symptomatic
splenomegaly
3. Massive nodes (ie, at least 10 cm in longest diameter) or progressive or symptomatic
lymphadenopathy
4. Progressive lymphocytosis with an increase of more than 50% over a 2-month period or
lymphocyte doubling time (LDT) of less than 6 months.
5. Constitutional symptoms, defined as any one or more of the following disease-related
symptoms or signs:
1. Unintentional weight loss of 10% or more within the previous 6 months;
2. Significant fatigue (ie, ECOG PS 2 or worse; inability to work or perform usual
activities);
3. Fevers higher than 100.5°F or 38.0°C for 2 or more weeks without other evidence
of infection; or
4. Night sweats for more than 1 month without evidence of infection.
5. Patients who have resistant disease after primary treatment
6. Patients who have a short time to progression after the first treatment (less
than 2 years)
OR
-Indolent or aggressive B-cell lymphoma (or other B-cell neoplasm) monoclonal for
Kappa-light chain with measurable disease after receiving at least one
chemotherapy regimen that includes Rituximab or an equivalent monoclonal antibody
OR
- Multiple myeloma monoclonal for Kappa-light chain with measurable disease
after receiving at least one chemotherapy regimen
- Life expectancy of at least 12 weeks or greater.
- Recovered from the toxic effects of all prior chemotherapy before entering
this study. PD1/PDL1 inhibitors will be allowed if medically indicated
- ANC > 500, Hgb greater than or equal to 7.0.
- Bilirubin less than 3 times the upper limit of normal.
- AST less than 5 times the upper limit of normal.
- Estimated GFR > 50mL/min
- Pulse oximetry of > 90% on room air
- Karnofsky score of > 60%.
Negative serology for HIV.
- Available autologous transduced peripheral blood T-cells with 15% or more
expression of CAR-Kappa determined by flow-cytometry.
- Patients must sign an informed consent indicating that they are aware this
is a research study and have been told of its possible benefits and toxic
side effects. Patients will be given a copy of the consent form.
- Sexually active patients must be willing to utilize one of the more
effective birth control methods during the study and for 3 months after the
study is concluded. The male partner should use a condom.
- If patient has CLL, must have negative Coombs test.
EXCLUSION CRITERIA:
BLOOD PROCUREMENT:
- Active infection requiring antibiotics
- Active autoimmune disease
T CELL TREATMENT:
- Symptomatic cardiac disease.
- History of hypersensitivity reactions to murine protein-containing products.
Currently receiving any investigational agents within the previous six weeks
or received any tumor vaccines within the previous 6 weeks.
- Tumor in a location where enlargement could cause airway obstruction.
- Pregnant or lactating.
We found this trial at
2
sites
Texas Children's Hospital Texas Children's Hospital, located in Houston, Texas, is a not-for-profit organization whose...
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Houston Methodist Hospital Houston Methodist is comprised of a leading academic medical center in the...
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