Combination Transfer of αCD19-TCRz-41BB and αCD22-TCRz-41BB CAR-T Cells for B-cell Hematologic Malignancy

NCT02903810 | Unknown Phase 1

• 1 other identifier: XZCJ20160001
• Study Type: interventional
• Target: 20
• Locations: 1 country
• Sites: 1

Brief Summary

Clinical study of CD19 CAR-T in the treatment of blood and lymphatic system tumor has been achieved a breakthrough. The main solution in clinical research is to use CD19 CAR-T infusion alone. Because of the heterogeneity of the tumor, the patient often carries tumor cells with CD19 deficient but other positive target antigens (such as CD22). Specifically removal of CD19 positive tumor cells in CAR-T treatment, CD19 negative tumor cells or tumor cells which carry other target antigens would amplify with extra free space released at the same time, resulting in the relapse of tumors of heterogeneities. In order to effectively control the recurrence, CAR-T treatment scheme specific for several target antigens was presented and verified. However treatment with the sequential infusion of different target specific CAR-T cells, the window period between two times infusions may be the opportunity for the tumor recurrence of heterogeneity; and bispecific CAR-T has also been reported only one CAR can be fully functioned. In order to avoid these problems, this topic puts forward for the first time in the international with a treatment scheme of an equal amount of infusion of CD19-41BB and CD22-41BB two Car-T in the treatment of refractory hematologic malignancies. We expect the treatment is more effective in eliminating tumor burden, and also can inhibit the recurrence of tumor heterogeneity at the same time.

Conditions

Hematopoietic/Lymphoid Cancer

Outcome Measures

Primary Outcomes (1)

• Safety (incidence of adverse events defined as dose-limited toxicity)

  30 days

Secondary Outcomes (5)

• Survival of CAR T cells in circulation measured by flow cytometry and qPCR

  1 years

• Overall complete remission rate

  8 weeks

• Tissue infiltration of transferred CAR-T cells

  1 years

• In vitro killing potential of infiltrated CAR-T cells

  1 years

• Phenotype of infused CAR-T cells

  1 years

Study Arms (1)

Mixed CAR-T Transfer

EXPERIMENTAL

All subjects will be infused with αCD19-TCRz-41BB and αCD22-TCRz-41BB CAR-T cells in equal number

Biological: Mixed CAR-T Transfer

Interventions

Mixed CAR-T Transfer BIOLOGICAL

All subjects will be infused with αCD19-TCRz-41BB and αCD22-TCRz-41BB CAR-T cells in equal number

Mixed CAR-T Transfer

Eligibility Criteria

• Age: 18 Years - 70 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Years to 70 Years, Male and female
• Expected survival \> 12 weeks
• Performance score 0-2
• Histologically confirmed as CD19/22-positive lymphoma/leukemia and who meet one of the following conditions; Patient receive at least 2-4 prior combination chemotherapy regimens (not including single agent monoclonal antibody therapy) and fail to achieve CR; or have disease recurrence; or not eligible for allogeneic stem cell transplantation; or disease responding or stable after most recent therapy but refused further treatment; Disease recurrence after stem cell transplantation; Diagnosis as lymphoma, but refuse conventional treatment such as chemotherapy, radiation, stem cell transplantation and monoclonal antibody therapy
• Creatinine \< 2.5 mg/dl;
• ALT/AST \< 3x normal;
• Bilirubin \< 2.0 mg/dl;
• Adequate venous access for apheresis, and no other contraindications for leukapheresis;
• Take contraceptive measures before recruit to this trial;
• Written voluntary informed consent is given.

You may not qualify if:

• Patients with symptoms of central nervous system
• Accompanied by other malignant tumor
• Active hepatitis B or C, HIV infection
• Any other diseases could affect the outcome of this trial
• Suffering severe cardiovascular or respiratory disease
• Poorly controlled hypertension
• A history of mental illness and poorly controlled
• Taking immunosuppressive agents within 1 week due to organ transplantation or other disease which need long-lasting administration
• Occurrence of unstable pulmonary embolism, deep vein thrombosis, or other major arterial/venous thromboembolic events 30 days prior to assignment
• Reaching a steady dose if receiving anticoagulant therapy before assignment
• Female study participants of reproductive potential must have a negative serum or urine pregnancy test performed within 48 hours before infusion
• Pregnant or lactating women
• Subject suffering disease affects the understanding of informed consent or comply with study protocol

Sponsors & Collaborators

• Xuzhou Medical University: lead

Study Sites (1)

XuZhou Medical University

Xuzhou, Jiangsu, China

RECRUITING

MeSH Terms

Conditions

Hematologic Neoplasms

Condition Hierarchy (Ancestors)

Neoplasms by Site; Neoplasms; Hematologic Diseases; Hemic and Lymphatic Diseases

Study Officials

• Jiang Cao, Doctor

  Xuzhou Medical University

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Jiang Cao, Doctor

CONTACT

138-5243-2263; CaoJiangClinicalTrial@outlook.com

Qingzhu Jia, Doctor

CONTACT

152-2333-4184; jiaqingzhu0801@outlook.com

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Director of Hematology

Study Record Dates

• First Submitted: September 13, 2016
• First Posted: September 16, 2016
• Study Start: September 1, 2016
• Primary Completion: December 1, 2018
• Study Completion: December 1, 2019
• Last Updated: October 12, 2016

Record last verified: 2016-10

Locations

CN (1)