Phase 1 Study of HER2-Specific CAR T Cell Locoregional Immunotherapy for HER2 Positive Recurrent/Refractory Pediatric Central Nervous System Tumors

Who is this study for? Patients with HER2 positive recurrent/refractory pediatric central nervous system tumors
What treatments are being studied? HER2-specific chimeric antigen receptor T cell
Status: Recruiting
Location: See location...
Intervention Type: Biological
Study Type: Interventional
Study Phase: Phase 1
SUMMARY

This is a Phase 1 study of central nervous system (CNS) locoregional adoptive therapy with autologous CD4 and CD8 T cells lentivirally transduced to express a HER2-specific chimeric antigen receptor (CAR) and EGFRt, delivered by an indwelling catheter in the tumor resection cavity or ventricular system in children and young adults with recurrent or refractory HER2-positive CNS tumors. A child or young adult with a refractory or recurrent CNS tumor will have their tumor tested for HER2 expression by immunohistochemistry (IHC) at their home institution or at Seattle Children's Hospital. If the tumor is HER2 positive and the patient meets all other eligibility criteria, including having a CNS catheter placed into the tumor resection cavity or into their ventricular system, and meets none of the exclusion criteria, then they can be apheresed, meaning T cells will be collected. The T cells will then be bioengineered into a second-generation CAR T cell that targets HER2-expressing tumor cells. The patient's newly engineered T cells will then be administered via the indwelling CNS catheter for two courses. In the first course they will receive a weekly dose of CAR T cells for three weeks, followed by a week off, an examination period, and then another course of weekly doses for three weeks. Following the two courses, patient's will undergo a series of studies including MRI to evaluate the effect of the CAR T cells and may have the opportunity to continue receiving additional courses of CAR T cells if the patient has not had adverse effects and if more of their T cells are available. The hypothesis is that an adequate amount of HER2-specific CAR T cells can be manufactured to complete two courses of treatment with three doses given on a weekly schedule followed by one week off in each course. The other hypothesis is that HER-specific CAR T cells safely can be administered through an indwelling CNS catheter to allow the T cells to directly interact with the tumor cells for each patient enrolled on the study safely can be delivered directly into the brain via indwelling catheter. Secondary aims of the study will include to evaluate CAR T cell distribution with the cerebrospinal fluid (CSF), the extent to which CAR T cells egress or traffic into the peripheral circulation or blood stream, and, if tissues samples from multiple time points are available, also evaluate the degree of HER2 expression at diagnosis versus at recurrence.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 1
Maximum Age: 26
Healthy Volunteers: No
View:

• Age ≥ 1 and ≤ 26 years

• Histologically diagnosed HER2-positive Central Nervous System (CNS) tumor

• Evidence of refractory or recurrent CNS disease for which there is no standard therapy

• Able to tolerate apheresis, or has apheresis product available for use in manufacturing

• CNS reservoir catheter, such as an Ommaya or Rickham catheter

• Life expectancy ≥ 8 weeks

• Lansky or Karnofsky score ≥ 60

• If patient does not have previously obtained apheresis product, patient must have recovered from acute toxic effects of all prior chemotherapy, immunotherapy, and radiotherapy and discontinue the following prior to enrollment:

• ≥ 7 days post last chemotherapy/biologic administration

• 3 half-lives or 30 days, whichever is shorter post last dose of anti-tumor antibody therapy

• Must be at least 30 days from most recent cell infusion

• All systemically administered corticosteroid treatment therapy must be stable or decreasing within 1 week prior to enrollment with maximum dexamethasone dose of 2.5 mg/m2/day. Corticosteroid physiologic replacement therapy is allowed.

• Adequate organ function

• Adequate laboratory values

• Patients of childbearing/fathering potential must agree to use highly effective contraception

Locations
United States
Washington
Seattle Children's Hospital
Recruiting
Seattle
Contact Information
Primary
Nicholas Vitanza, MD
CBDCIntake@seattlechildrens.org
206-987-2106
Time Frame
Start Date: July 26, 2018
Estimated Completion Date: July 26, 2039
Participants
Target number of participants: 48
Treatments
Experimental: ARM A (Tumor Cavity Infusion)
patients with supratentorial tumors for which CAR T cells will be delivered into the tumor resection cavity~Intervention: HER2-specific chimeric antigen receptor (CAR) T cell
Experimental: ARM B (Ventricular System Infusion)
patients with either infratentorial tumors or leptomeningeal tumors for which the CAR T cells will be delivered into the fourth ventricle or lateral ventricle, respectively~Intervention: HER2-specific chimeric antigen receptor (CAR) T cell
Sponsors
Leads: Seattle Children's Hospital

This content was sourced from clinicaltrials.gov

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