Anti-CD22 Chimeric Receptor T Cells in Pediatric and Young Adults With Recurrent or Refractory CD22-expressing B Cell Malignancies

• ClinicalTrials.gov Identifier: NCT02315612
• Recruitment Status: Recruiting
• First Posted: December 12, 2014
• Last Update Posted: June 5, 2023
• Sponsor: National Cancer Institute (NCI)
• Information provided by (Responsible Party): National Institutes of Health Clinical Center (CC) ( National Cancer Institute (NCI) )

Study Description

Brief Summary:

Background:

- One type of cancer therapy takes blood cells from a person, changes them in a lab, then gives the cells back to the person. In this study, researchers are using an anti-CD22 gene, a virus, and an immune receptor to change the cells.

Objective:

- To see if giving anti-CD22 Chimeric Antigen Receptor (CAR) cells to young people with certain cancers is safe and effective.

Eligibility:

- People ages 1-39 with a leukemia or lymphoma that has not been cured by standard therapy.

Design:

• Participants will be screened to ensure their cancer cells express the CD22 protein. They will also have medical history, physical exam, blood and urine tests, heart tests, scans, and x-rays. They may give spinal fluid or have bone marrow tests.
• Participants may have eye and neurologic exams.
• Participants will get a central venous catheter or a catheter in a large vein.
• Participants will have white blood cells removed. Blood is removed through a needle in an arm. White blood cells are removed. The rest of the blood is returned by needle in the other arm.
• The cells will be changed in a laboratory.
• Participants will get two IV chemotherapy drugs over 4 days. Some will stay in the hospital for this.
• All participants will be in the hospital to get anti-CD22 CAR cells through IV. They will stay until any bad side effects are gone.
• Participants will have many blood tests. They may repeat some screening exams.
• Participants will have monthly visits for 2-3 months, then every 3-6 months. They may repeat some screening exams.
• Participants will have follow-up for 15 years.

Condition or disease	Intervention/treatment	Phase
Follicular Lymphoma; ALL; NHL; Large Cell Lymphoma	Biological: CD22-CAR	Phase 1

Detailed Description:

Background:

• Adoptive cellular therapy with T cells genetically modified using viral-based vectors to express chimeric antigen receptors targeting the CD19 molecule have demonstrated dramatic clinical responses in patients with acute lymphoblastic leukemia (ALL). However, not all patients respond and CD19-negative escape has been observed following CD19 CAR therapy, as well as anti-CD19/CD3 bispecific antibody therapy. Thus, additional targets are needed.
• CD22 is a B-lineage-restricted, transmembrane phosphoglycoprotein of the Ig superfamily that is widely expressed on B-cell malignancies including 96% to 100% of pediatric Bprecursor ALL. Therefore, CD22 represents a promising target. Encouraging responses targeting CD22 with an antibody based immunoconjugate have been seen in patients, including children, with recurrent and refractory ALL. This will be the first in human testing of anti-CD22 CAR adoptive cell therapy.

Objectives:

• To determine the feasibility of producing anti-CD22 CAR cells meeting established release criteria. Complete
• To assess the safety of administering escalating doses of anti-CD22-CAR engineered T cells in children and young adults with recurrent or refractory CD22- expressing B cell malignancies following a cyclophosphamide/fludarabine preparative regimen.

Eligibility:

- Patients 3-39 years of age, at least 14.5 kg, with CD22-expressing B-cell malignancies that have recurred after or not responded to one or more standard regimens and deemed incurable by standard therapy. Patients with a history of allogeneic hematopoietic transplantation (SCT) who meet all eligibility criteria are eligible to participate. Patients previously treated with anti-CD19 CAR engineered T cells are also eligible.

Design:

• PBMC will be obtained by leukapheresis, CD3+ cells enriched and cultured in the presence of anti-CD3/-CD28 beads followed by lentiviral vector supernatant containing the anti-CD22 (M971BBz) CAR.
• On Day -4 (cell infusion is Day 0), patients will begin induction chemotherapy comprising fludarabine 25 mg/m2 on Days -4, -3, and -2 and cyclophosphamide 900 mg/m2 on day -2.
• The CD22-CAR cells will be infused on Day 0, with up to a 72h delay allowed for infusion of fresh cells or a 7 day delay if cells are cryopreserved, if needed for resolution of clinical toxicities, to generate adequate cell numbers, or to facilitate scheduling.
• A phase I cell dose escalation scheme will be performed using 3 dose levels (3 x 10(5) transduced T cells/kg; 1 x 10(6) transduced T cells/kg; and 3 x 10(6) transduced T cells/kg;). If 2/6 patients have DLT at dose level 1, safety will be evaluated in a de-escalated dose of 1 x 10(5) transduced T cells/kg (more or less 20%)). Once the maximum tolerated dose (or highest level evaluated) is reached, enrollment into an expansion cohort of a total of 83 patients at MTD will proceed to provide additional information regarding the feasibility, safety and efficacy of this treatment.
• Patients will be monitored for toxicity, response and T cell persistence as well as other biologic correlates.

Study Design

• Study Type: Interventional (Clinical Trial)
• Estimated Enrollment: 208 participants
• Allocation: Non-Randomized
• Intervention Model: Sequential Assignment
• Masking: None (Open Label)
• Primary Purpose: Treatment
• Official Title: Phase I Dose Escalation Study of Anti-CD22 Chimeric Receptor T Cells in Pediatric and Young Adults With Recurrent or Refractory CD22-expressing B Cell Malignancies
• Actual Study Start Date: December 12, 2014
• Actual Primary Completion Date: April 3, 2019
• Estimated Study Completion Date: June 1, 2040

Arms and Interventions

Arm	Intervention/treatment
Experimental: Arm 1; dose escalation of CD22-CAR	Biological: CD22-CAR; CD22-CAR cells will be infused on Day 0 after induction chemotherapy regimen.
Experimental: Arm 2; dose expansion of CD22-CAR	Biological: CD22-CAR; CD22-CAR cells will be infused on Day 0 after induction chemotherapy regimen.

Outcome Measures

Primary Outcome Measures :

1. Toxicity [ Time Frame: End of treatment ]
   Number of patients who have grade 3 CRS and above
2. Response [ Time Frame: 1 month, 3 months, and 6 months following CAR infusion ]
   Number of patients who have complete and partial remission

Secondary Outcome Measures :

1. Safety and Toxicity [ Time Frame: 1 month, 3 months and 6 months following CAR infusion ]
   Number of patients who have detectable CAR cells
2. Objective Response (Complete + Partial Remission) [ Time Frame: 1 month, 3 months and 6 months following CAR infusion ]
   The number of patients who have complete and partial remissions
3. CAR-T cell Persistence [ Time Frame: 1 month, 3 months and 6 months following CAR infusion ]
   The number of patients who have detectable CAR cells

Eligibility Criteria

• Ages Eligible for Study: 3 Years to 39 Years (Child, Adult)
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Criteria

-INCLUSION CRITERIA:

1. Patient must have a B cell ALL (inclusive of ALL blast transformation from CML) or lymphoma and must have relapsed or refractory disease after at least one standard chemotherapy regimen and one salvage regimen. In view of the PI and the primary oncologist, there must be no available alternative curative therapies and subjects must be either ineligible for allogeneic stem cell transplant (SCT), have refused SCT, recurred after SCT, or have disease activity that prohibits SCT at the time of enrollment.
2. CD22 expression must be detected on greater than 15% of the malignant cells by immunohistochemistry or greater than 80% by flow cytometry. The choice of whether to use flow cytometry or immunohistochemistry will be determined by what is the most easily available tissue sample in each patent. In general, immunohistochemistry will be used for lymph node biopsies, flow cytometry will be used for peripheral blood and bone marrow samples and CSF when feasible.
3. Patients must have measurable or evaluable disease at the time of enrollment, which may include any evidence of disease including minimal residual disease detected by flow cytometry, cytogenetics, or polymerase chain reaction (PCR) analysis.
4. Greater than or equal to 3 years of age (and at least 14.5 kg) and less than or equal to 39 years of age at time of enrollment.
5. Subjects with CNS disease are eligible, with exceptions as noted in the exclusion criteria
6. Patients, parents/guardian(s), legally authorized representative (LAR), or durable power of attorney must be able to give consent and sign the informed consent document.
7. Clinical performance status: Patients greater than or equal to 16 years of age: Karnofsky greater than or equal to 50%; Patients < 16 years of age: Lansky scale greater than or equal to 50%. Subjects who are unable to walk because of paralysis, but who are upright in a wheelchair will be considered ambulatory for the purpose of calculating the performance score.
8. Patients of child-bearing or child-fathering potential must be willing to practice birth control from the time of enrollment on this study and for four months after receiving the preparative regimen.

9. Patients must have adequate organ function as described below:

   -Cardiac function: Left ventricular ejection fraction greater than or equal to 45% or fractional shortening greater than or equal to 28%.

   -Pulmonary function: Patients without respiratory symptoms (e.g. dyspnea at rest, known requirement for supplemental oxygen therapy) and who have an oxygen saturation greater than or equal to 92% on room air, will be eligible. For patients not meeting this criteria, pulmonary function tests will be performed to confirm that the DLCO/VA/Adj is 50% of the normal predicted value corrected for hemoglobin and alveolar volume in order to meet eligibility.(For children who are unable to cooperate for PFTs, the criterion is: No evidence of dyspnea at rest, no exercise intolerance and no requirement for supplemental oxygen therapy. )

   • Hematologic function:

     --Absolute neutrophil count greater than or equal to 750/mcL

     --Platelets greater than or equal to 50,000/mcl

     • A subject will not be excluded because of pancytopenia related to disease

   • Liver Function:

     • AST (SGOT)/ALT (SGPT): less than or equal to 20 x institutional upper limit of normal
     • Total bilirubin less than or equal to 2 x ULN (ecept in the case of subjects with documented Gilbert s disease greater than or equal to 3 x ULN)

   • Renal Function: Normal creatinineCreatinine level < the maximum for age listed in the table below OR creatinine clearance greater than or equal to 60 mL/min/1.73 m2 for patients with creatinine levels above institutional normal.

     • less than or equal to 5 years old: maximum serum creatinine 0.8mg/dL
     • between 6 and 10 years old: maximum serum creatinine 1.0mg/dL
     • greater than 10 years old: maximum serum creatinine 1.2mg/dL
10. Patients previously treated with anti-CD19 CAR or other adoptive cell therapies will be eligible if all other eligibility criteria in the expansion phase. Circulating CAR T cells must be <5% in peripheral blood.

EXCLUSION CRITERIA:

Subjects meeting any of the following criteria are not eligible for participation in the study:

1. Subjects with radiologically-detected active CNS lymphoma, leptomeningeal CNS disease or isolated CNS disease which are eligible for definitive CNS directed radiationtherapy will be excluded.

2 .Hyperleukocytosis (greater than or equal to 50,000 blasts/ L) or rapidly progressive disease that in theestimation of the investigator and sponsor would compromise ability to complete study therapy;

3. Pregnant or breast-feeding females

4. Recent prior therapy

5. Subjects will be excluded related to the following prior therapy criteria:

• Systemic chemotherapy, anti-neoplastic investigational agents, or antibody based therapies 2 weeks (6 weeks for clofarabine or nitrosoureas) prior to apheresis with the following exception:

  --No time restriction with prior intrathecal chemotherapy, steroid therapy, hydroxyurea or ALL maintenance type chemotherapy (vincristine, 6-mercaptopurine, oral methotrexate, or a tyrosine kinase inhibitor for patients with Ph+ ALL) provided there is recovery from any acute toxic effects.

• Radiation therapy <= 3 weeks prior to apheresis with the following exception:

  --No time restriction with radiation therapy if the volume of bone marrow treated is less than 10% and the subject has measurable/evaluable disease outside the radiation window.

• History of allogeneic stem cell transplantation prior to apheresis that meet the following criteria:

  • Less than 100 days post-transplant
  • Evidence of active graft-versus-host disease (GVHD)
  • Taking immunosuppressive agents within 30 days prior to apheresis.
  • Less than 6 weeks post donor lymphocyte infusion (DLI)

• History of prior CAR therapy or other adoptive cell therapies prior to apheresis that meet the following criteria:

  • Less than 30 days post-infusion

  • Circulating CAR T cells (or genetically modified cells) >=5% by flow cytometry in peripheral blood

    6. HIV/HBV/HCV Infection:

    1. Seropositive for HIV antibody. (Patients with HIV are at increased risk of lethal infections when treated with marrow-suppressive therapy. Appropriate studies will beundertaken in patients receiving combination antiretroviral therapy in the future should study results indicate effectiveness.)
    2. Positive for Hepatitis B surface antigen (HbsAG)

    3. Evidence of active HCV (evidenced by detectable HCV RNA)

       7. Uncontrolled, symptomatic, intercurrent illness including but not limited to infection, congestive heart failure, unstable angina pectoris, cardiac arrhythmia, psychiatric illness, or social situations that would limit compliance with study requirements or in the opinion of the PI would pose an unacceptable risk to the subject;

       8. Second malignancy other than in situ carcinoma of the cervix, unless the tumor was treated with curative intent at least two years previously and subject is in remission;

       9. History of severe, immediate hypersensitivity reaction attributed to compounds of similar chemical or biologic composition to any agents used in study or in the manufacturing of the cells (i.e. gentamicin)

Contacts and Locations

Contacts

Contact: NCI Pediatric Leukemia, Lymphoma Transpl; (240) 760-6970; NCILLTCT@mail.nih.gov

Contact: Nirali N Shah, M.D.; (240) 760-6970; shahnn@mail.nih.gov

Locations

United States, Maryland

National Institutes of Health Clinical Center; Recruiting

Bethesda, Maryland, United States, 20892

Contact: For more information at the NIH Clinical Center contact Office of Patient Recruitment (OPR) 800-411-1222 ext TTY dial 711 ccopr@nih.gov

Sponsors and Collaborators

National Cancer Institute (NCI)

Investigators

• Principal Investigator: Nirali N Shah, M.D.; National Cancer Institute (NCI)

More Information

Additional Information:

NIH Clinical Center Detailed Web Page 

Publications:

Haso W, Lee DW, Shah NN, Stetler-Stevenson M, Yuan CM, Pastan IH, Dimitrov DS, Morgan RA, FitzGerald DJ, Barrett DM, Wayne AS, Mackall CL, Orentas RJ. Anti-CD22-chimeric antigen receptors targeting B-cell precursor acute lymphoblastic leukemia. Blood. 2013 Feb 14;121(7):1165-74. doi: 10.1182/blood-2012-06-438002. Epub 2012 Dec 14.

Bang S, Nagata S, Onda M, Kreitman RJ, Pastan I. HA22 (R490A) is a recombinant immunotoxin with increased antitumor activity without an increase in animal toxicity. Clin Cancer Res. 2005 Feb 15;11(4):1545-50. doi: 10.1158/1078-0432.CCR-04-1939.

Kalos M, June CH. Adoptive T cell transfer for cancer immunotherapy in the era of synthetic biology. Immunity. 2013 Jul 25;39(1):49-60. doi: 10.1016/j.immuni.2013.07.002.

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):

Masih KE, Ligon JA, Yates B, Shalabi H, Little L, Islam Z, Ombrello AK, Inglefield J, Nussenblatt V, Manion M, Khan J, Shah NN. Consequences of hemophagocytic lymphohistiocytosis-like cytokine release syndrome toxicities and concurrent bacteremia. Pediatr Blood Cancer. 2021 Oct;68(10):e29247. doi: 10.1002/pbc.29247. Epub 2021 Jul 26.

Shah NN, Highfill SL, Shalabi H, Yates B, Jin J, Wolters PL, Ombrello A, Steinberg SM, Martin S, Delbrook C, Hoffman L, Little L, Ponduri A, Qin H, Qureshi H, Dulau-Florea A, Salem D, Wang HW, Yuan C, Stetler-Stevenson M, Panch S, Tran M, Mackall CL, Stroncek DF, Fry TJ. CD4/CD8 T-Cell Selection Affects Chimeric Antigen Receptor (CAR) T-Cell Potency and Toxicity: Updated Results From a Phase I Anti-CD22 CAR T-Cell Trial. J Clin Oncol. 2020 Jun 10;38(17):1938-1950. doi: 10.1200/JCO.19.03279. Epub 2020 Apr 14.

• Responsible Party: National Cancer Institute (NCI)
• ClinicalTrials.gov Identifier: NCT02315612
• Other Study ID Numbers: 150029; 15-C-0029
• First Posted: December 12, 2014
• Last Update Posted: June 5, 2023
• Last Verified: June 1, 2023

Individual Participant Data (IPD) Sharing Statement:

• Plan to Share IPD: Yes
• Plan Description: .All IPD recorded in the medical record will be shared with intramural investigators upon request.
• Supporting Materials: Study Protocol; Statistical Analysis Plan (SAP); Informed Consent Form (ICF)
• Time Frame: Clinical data available during the study and indefinitely.
• Access Criteria: Clinical data will be made available via subscription to BTRIS and with the permission of the study PI.

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

Keywords provided by National Institutes of Health Clinical Center (CC) ( National Cancer Institute (NCI) ):

CD-22 Expressing Tumor; Chimeric Antigen Receptor; Adoptive Immunotherapy; ALL; Lymphoma

Additional relevant MeSH terms:

Lymphoma; Neoplasms by Histologic Type; Neoplasms; Lymphoproliferative Disorders; Lymphatic Diseases; Immunoproliferative Disorders; Immune System Diseases