A Phase 1 Study of CD22-CAR TCell Immunotherapy for CD22+ Leukemia and Lymphoma (PLAT-04)

• ClinicalTrials.gov Identifier: NCT03244306
• Recruitment Status: Active, not recruiting
• First Posted: August 9, 2017
• Last Update Posted: February 16, 2022
• Sponsor: Seattle Children's Hospital
• Information provided by (Responsible Party): Rebecca Gardner, Seattle Children's Hospital

Study Description

Brief Summary:

Patients with relapsed or refractory leukemia often develop resistance to chemotherapy and some patients who relapse following CD19 directed therapy relapse with CD19 negative leukemia. For this reason, the investigators are attempting to use T-cells obtained directly from the patient, which can be genetically modified to express a chimeric antigen receptor (CAR) to CD22, a different protein from CD19, expressed on the surface of the leukemic cell in patients with CD22+ leukemia. The CAR enables the T-cell to recognize and kill the leukemic cell through the recognition of CD22, a protein expressed on the surface of the leukemic cell in patients with CD22+ leukemia. This is a Phase 1 study designed to determine the safety and feasibility of the CAR+ T - cells and the feasibility of making enough to treat patients with CD22+ leukemia.

Condition or disease	Intervention/treatment	Phase
Leukemia	Biological: Patient-derived CD22-specific CAR T-cells also expressing an EGFRt	Phase 1

Study Design

• Study Type: Interventional (Clinical Trial)
• Actual Enrollment: 4 participants
• Allocation: N/A
• Intervention Model: Single Group Assignment
• Masking: None (Open Label)
• Primary Purpose: Treatment
• Official Title: Pediatric and Young Adult Leukemia Adoptive Therapy (PLAT)-04: A Phase 1 Feasibility and Safety Study of CD22-CAR T Cell Immunotherapy for CD22+ Leukemia and Lymphoma
• Actual Study Start Date: July 27, 2017
• Actual Primary Completion Date: November 14, 2018
• Estimated Study Completion Date: July 2035

Arms and Interventions

Arm	Intervention/treatment
Experimental: Autologous CD22-specific CAR T-cells expressing EGFRt	Biological: Patient-derived CD22-specific CAR T-cells also expressing an EGFRt; Patient-derived CD22-specific chimeric antigen receptor T-cells expressing an EGFRt

Outcome Measures

Primary Outcome Measures :

1. The adverse events associated with one or multiple CAR T-cell product infusions will be assessed [ Time Frame: 30 days ]
   The type, frequency, severity, and duration of adverse events will be summarized
2. The number of successfully and unsuccessfully manufactured and infused CAR T-cell products will be assessed [ Time Frame: 28 days ]
   Proportion of products successfully manufactured and infused

Eligibility Criteria

• Ages Eligible for Study: 1 Year to 26 Years (Child, Adult)
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Criteria

Inclusion Criteria:

• First 3 subjects: male and female subjects age ≥ 18 years and < 27 years
• Subsequent subjects: 12 months of age and <27 years of age at the time of study enrollment

• Disease status (one of the following):

  1. If post-allogeneic hematopoetic cell transplant (HCT): confirmed CD22+ leukemia recurrence, defined as ≥0.01% disease

  2. If Relapse/Refractory status with no prior history of allogeneic HCT, one of:

     • 2nd or grater marrow relapse, with or without extramedullary disease
     • 1st marrow relapse at end of 1st month of re-induction with marrow having ≥0.01% blasts by morphology and/or MPF
     • Primary Refractory, defined as >5% blasts by multi-parameter flow after ≥2 separate induction regimens
     • Subject has indication for HCT but is ineligible, inclusive of persistent minimal residual disease
  3. CD22+ Lymphoma refractory or relapsed with no known curative therapies available
• Asymptomatic from CNS involvement, if present, and have a reasonable expectation that disease burden can be controlled in the interval between enrollment and T-cell infusion. Subjects with significant neurologic deterioration will not be eligible for T-cell infusion until stabilized.
• Free from active GVHD and off immunosuppressive GVHD therapy for 4 weeks.
• Lansky or Karnofsky performance score of ≥50
• Life expectancy of >8 weeks
• Recovered from acute toxic effects of all prior chemotherapy, immunotherapy, and radiotherapy
• ≥7 days post last chemotherapy administration (excluding intrathecal or maintenance chemotherapy)
• ≥7 days post last systemic corticosteroid administration
• No prior virotherapy
• Adequate organ function
• Adequate laboratory values
• Patients of childbearing/fathering potential must agree to use highly effective contraception
• Signed a written consent

Exclusion Criteria:

• Presence of active clinically significant CNS dysfunction
• Pregnant or breastfeeding
• Unable to tolerate apheresis procedure, including placement of temporary apheresis line if required
• Presence of active malignancy other than CD22+ leukemia or lymphoma
• Presence of active severe infection
• Presence of any concurrent medical condition that would prevent the patient from undergoing protocol-based therapy
• Presence of primary immunodeficiency/bone marrow failure syndrome
• Unwilling to participate in 15-year follow-up period that is required if CAR T cell therapy is administered

Contacts and Locations

Locations

United States, Washington

Seattle Children's Hospital

Seattle, Washington, United States, 98105

Sponsors and Collaborators

Seattle Children's Hospital

Investigators

• Study Chair: Corinne Summers, MD; Seattle Children's Hospital

More Information

• Responsible Party: Rebecca Gardner, Associate Medical Director, Immunotherapy Coordinating Center, Seattle Children's Hospital
• ClinicalTrials.gov Identifier: NCT03244306
• Other Study ID Numbers: PLAT-04
• First Posted: August 9, 2017
• Last Update Posted: February 16, 2022
• Last Verified: February 2022

• Studies a U.S. FDA-regulated Drug Product: Yes
• Studies a U.S. FDA-regulated Device Product: No

Keywords provided by Rebecca Gardner, Seattle Children's Hospital:

leukemia; CD 22; CAR T cell; pediatric; young adult; chimeric antigen receptor

Additional relevant MeSH terms:

Leukemia; Neoplasms by Histologic Type; Neoplasms