Adoptive Cellular Immunotherapy for Progressive Multifocal Leukoencephalopathy With Ex Vivo Generated Polyomavirus-Specific T-Cells
| Status: | Active, not recruiting |
|---|---|
| Conditions: | Neurology |
| Therapuetic Areas: | Neurology |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 3/2/2019 |
| Start Date: | March 28, 2016 |
| End Date: | July 1, 2020 |
A Pilot Study of Adoptive Cellular Immunotherapy for Progressive Multifocal Leukoencephalopathy With Ex Vivo Generated Polyomavirus-Specific T-cells
Background:
Progressive Multifocal Leukoencephalopathy (PML) is a brain infection in people with a
weakened immune system. Researchers think polyoma virus specific T cells (PyVST) therapy can
treat PML. The PyVST cells are made from blood cells of a healthy relative. They are grown in
a lab to expand the virus-killing cells, then given to the person with PML.
Objective:
To test whether PyVST safely treats PML.
Eligibility:
- Adults ages 18 and older with PML
- Healthy adults ages 18 and older who have:
- Been screened under protocol 97-H-0041
- A sibling, parent, or child with PML and matching cells
Design:
- Participants will be screened with:
- Medical history
- Physical exam
- Blood and urine tests
- PML participants will also be screened with:
- Cerebrospinal fluid removed by needle in the back.
- MRI: A dye is injected in a vein. They lie on a table that slides into a cylinder.
- Questionnaires
Healthy participants will have apheresis: Blood flows through a needle in one arm into
machine that separates blood cells needed for donation. The rest of the blood is returned by
needle to the other arm. Some participants may have a central line placed in a vein instead.
They can have apheresis up to 3 times, at least 28 days apart.
Participants with PML will receive the PyVST cells by needle in the arm. They will stay in
the hospital 1 week. They can do this up to 3 times, at least 28 days apart. After each
infusion, they will have weekly visits for 1 month. Then they will have 4 visits over 1 year.
Visits include repeats of screening tests.
Progressive Multifocal Leukoencephalopathy (PML) is a brain infection in people with a
weakened immune system. Researchers think polyoma virus specific T cells (PyVST) therapy can
treat PML. The PyVST cells are made from blood cells of a healthy relative. They are grown in
a lab to expand the virus-killing cells, then given to the person with PML.
Objective:
To test whether PyVST safely treats PML.
Eligibility:
- Adults ages 18 and older with PML
- Healthy adults ages 18 and older who have:
- Been screened under protocol 97-H-0041
- A sibling, parent, or child with PML and matching cells
Design:
- Participants will be screened with:
- Medical history
- Physical exam
- Blood and urine tests
- PML participants will also be screened with:
- Cerebrospinal fluid removed by needle in the back.
- MRI: A dye is injected in a vein. They lie on a table that slides into a cylinder.
- Questionnaires
Healthy participants will have apheresis: Blood flows through a needle in one arm into
machine that separates blood cells needed for donation. The rest of the blood is returned by
needle to the other arm. Some participants may have a central line placed in a vein instead.
They can have apheresis up to 3 times, at least 28 days apart.
Participants with PML will receive the PyVST cells by needle in the arm. They will stay in
the hospital 1 week. They can do this up to 3 times, at least 28 days apart. After each
infusion, they will have weekly visits for 1 month. Then they will have 4 visits over 1 year.
Visits include repeats of screening tests.
Objective
This pilot clinical trial will aim to determine the feasibility and potential toxicities
associated with treating patients with progressive multifocal leukoencephalopathy (PML) with
polyomavirus (PyV)-specific partially matched polyclonal allogeneic T cells. It will further
provide initial efficacy data for this indication.
Study Population
Up to 18 subjects with definite PML, defined as clinical signs and MRI compatible with active
PML and the presence of JCV by PCR in CSF. Subjects must be 18 years of age or older and must
have a first degree, partially HLA- matched relative able and willing to act as a donor of
lymphocytes. Subjects with underlying reversible immunosuppression (i.e.- HIV or MS status
post treatment with natalizumab), or subjects with uncontrolled malignancy will be excluded.
Subjects with evidence of active CNS inflammation as determined by presence of significant
contrast enhancement within the PML lesions by MRI will also be excluded because it is
assumed such patients are already mounting an adequate immune response against the infection.
Design
This will be a first-in-human pilot study assessing the feasibility and toxicity profile of
NIH PyVST cellular product in subjects with PML. Subjects will be screened under the existing
NIH Natural History study of PML (13-N-0017). Sequential enrollment will be spaced at least
28 days apart. An initial fixed dose PyVST infusion (target dose of 1 x 10(6) PyVST/kg (+/-
10%)) will be administered by intravenous (IV) infusion, followed by 2x 10(6) PyVST/kg
(+/-10%) up to 2 times to each subject if needed.
Outcome Measures
Safety will be monitored to 28 days continuously with stopping rules based on the
treatment-related serious adverse event rate. Secondary outcomes include survival, assessed
at day 28 and at 1 year following the last infusion. CSF viral titers, MR imaging, and
clinical disability scales will also be collected.
This pilot clinical trial will aim to determine the feasibility and potential toxicities
associated with treating patients with progressive multifocal leukoencephalopathy (PML) with
polyomavirus (PyV)-specific partially matched polyclonal allogeneic T cells. It will further
provide initial efficacy data for this indication.
Study Population
Up to 18 subjects with definite PML, defined as clinical signs and MRI compatible with active
PML and the presence of JCV by PCR in CSF. Subjects must be 18 years of age or older and must
have a first degree, partially HLA- matched relative able and willing to act as a donor of
lymphocytes. Subjects with underlying reversible immunosuppression (i.e.- HIV or MS status
post treatment with natalizumab), or subjects with uncontrolled malignancy will be excluded.
Subjects with evidence of active CNS inflammation as determined by presence of significant
contrast enhancement within the PML lesions by MRI will also be excluded because it is
assumed such patients are already mounting an adequate immune response against the infection.
Design
This will be a first-in-human pilot study assessing the feasibility and toxicity profile of
NIH PyVST cellular product in subjects with PML. Subjects will be screened under the existing
NIH Natural History study of PML (13-N-0017). Sequential enrollment will be spaced at least
28 days apart. An initial fixed dose PyVST infusion (target dose of 1 x 10(6) PyVST/kg (+/-
10%)) will be administered by intravenous (IV) infusion, followed by 2x 10(6) PyVST/kg
(+/-10%) up to 2 times to each subject if needed.
Outcome Measures
Safety will be monitored to 28 days continuously with stopping rules based on the
treatment-related serious adverse event rate. Secondary outcomes include survival, assessed
at day 28 and at 1 year following the last infusion. CSF viral titers, MR imaging, and
clinical disability scales will also be collected.
- INCLUSION CRITERIA - PATIENT:
- Clinically definite PML, defined as clinical signs and MRI compatible with active PML
and the presence of JCV by PCR in CSF
- Modified Rankin Scale 1-4, inclusive
- Age 18 or older
- Patient medically stable and able to tolerate travel to NIH
- Available PyVST
- Subjects of childbearing or child-fathering potential must be willing to use a
medically acceptable form of birth control, which includes abstinence, while they are
being treated on this study
- Willing and able to participate in all aspects of trial design and follow-up
- Able to provide informed consent at the time of study enrollment (not required for
reinfusions).
EXCLUSION CRITERIA - PATIENT:
- Patients with human immunodeficiency virus (HIV infection)
- Patients who have been treated with natalizumab
- Patients with readily reversible immunosuppressive state
- Patients receiving immunosuppressive or immunomodulatory therapies within 28 days of
screening for enrollment that could interfere with PyVST function
- Patients with other uncontrolled infections. For bacterial infections, patients must
be receiving definitive therapy and have no signs of progressing infection for 72
hours prior to enrollment. For fungal infections, patients must be receiving
definitive systemic anti-fungal therapy and have no signs of progressing infection for
1 week prior to enrollment.
- Patients who have received donor lymphocyte infusion (DLI) within 28 days
- Uncontrolled relapse of malignancy
- Patients with any other associated CNS disease that might confound outcomes
- Patients with contraindication to MRI (including cardiac pacemakers and some infusion
pumps, other metallic implants, metallic foreign objects)
- MRI findings consistent with immune system reconstitution inflammatory syndrome (IRIS)
and determined to be mounting an adequate immune response to the infection
- Patients with medical contraindication to LP
- For subjects who have previously received PyVST infusions, any treatment-limiting
toxicity (defined in Section 8.3) to previous infusions
- Subjects with a positive pregnancy test or who are nursing.
INCLUSION CRITERIA - DONOR:
- Ability to provide informed consent at the time of enrollment
- First degree relative of patient (sibling, parent/child)
- Age 18 or older
EXCLUSION CRITERIA - DONOR:
- Sickling hemoglobinopathies including HbSS and HbSC by history and peripheral blood
smear; donors with HbAS are acceptable
- HbsAg, anti-HBc, anti-HCV, anti-HIV, anti-HTLV, and RPR
- Cardiovascular instability, severe anemia, inadequate venous access, severe
coagulation disorder or any other medical condition that the Principal Investigator or
Apheresis Unit staff considers a contraindication to the apheresis procedure or
research blood draw.
- Positive pregnancy test
We found this trial at
1
site
9000 Rockville Pike
Bethesda, Maryland 20892
Bethesda, Maryland 20892
Phone: 800-411-1222
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