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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04340167
Other study ID # BR-22-C
Secondary ID
Status Recruiting
Phase Phase 2
First received
Last updated
Start date May 1, 2020
Est. completion date October 1, 2024

Study information

Verified date August 2022
Source Beijing Boren Hospital
Contact Jing Pan, Master
Phone +8618911067969
Email panj@borenhospital.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators will conduct a phase II clinical trial of autologous humanized anti-CD22 chimeric antigen receptor T cells treating refractory or relapsed B acute lymphoblastic leukemia children in Beijing Boren Hospital. The study will be approved by the institutional review board of Beijing Boren Hospital, and informed consent will be obtained in accordance with the Declaration of Helsinki. All these participants will be matched the diagnostic criteria for (r/r) B-ALL according to the WHO classification and complete morphological evaluation, immunophenotype analysis by flow cytometry (FCM), cytogenetic analysis by routine G-banding karyotype analysis and leukemia fusion gene screening by multiplex nested reverse transcriptase-polymerase chain reaction (PCR). Participants will be eligible if they are heavily treated B-ALL who failed from re-induction chemotherapy after relapse or continued MRD+ for more than three months, and had positive CD22 expression on leukemia blasts by FCM (>95% CD19). After CAR T-cell infusion, clinical outcomes including overall survival (OS), Disease-free survival (DFS), adverse effects and relapse will be evaluated.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date October 1, 2024
Est. primary completion date May 1, 2024
Accepts healthy volunteers No
Gender All
Age group 0 Years to 18 Years
Eligibility Inclusion Criteria: - Patients who were diagnosed as primary refractory or relapsed B-ALL. All the patients matched the diagnostic criteria of ALL according to the WHO classification and conducted morphological evaluation, immunophenotype analysis by flow cytometry (FCM), cytogenetic analysis by routine G-banding karyotype analysis, screen of 56 leukemia-related fusion genes by multiplex nested reverse transcriptase-polymerase chain reaction (RT-PCR), and quantification of fusion genes by real-time PCR with ABL1 as reference. - Extramedullary diseases (EMDs) were confirmed CD22+ by FCM and evaluated by positron emission tomography/computed tomography (PET/CT), CT, MRI or ultrasonography. - The patient relapsed during chemotherapy or failed from re-induction chemotherapy (including first and second-generation TKIs) after relapse or had a persistent positive minimal residual disease (MRD) for three months. Patients had positive CD22 expression on leukemia blasts by FCM (>95% CD22 positive); - Age from 0 to 18 years old; - Children candidates can be recruited after the legal guardian or patient advocate has signed the treatment consent form and voluntary consent form. Exclusion Criteria: - Intracranial hypertension or unconscious; - Acute heart failure or severe arrhythmia; - Acute respiratory failure; - Other types of malignant tumors; - Diffuse intravascular coagulation; - Serum creatinine and/or blood urea nitrogen over 1.5 times than normal range; - Sepsis or other uncontrolled infection; - Uncontrolled diabetes mellitus; - Severe psychological disorder; - Obvious cranial lesions with cranial MRI; - More than 20 counts/ul leukemic cells in cerebrospinal fluid; - More than 30% leukemic cells in the blood; - Stage III WHO/ECOG score; - Organ recipients; - Pregnant or breastfeeding; - Active, uncontrolled infection, including hepatitis B, hepatitis C or human immunodeficiency virus (HIV).

Study Design


Related Conditions & MeSH terms


Intervention

Biological:
Autologous humanized anti-CD22 chimeric antigen receptor T cells
CAR-T cells were manufactured from peripheral blood mononuclear cells collected by leukapheresis and frozen for multiple uses. Before each CAR T-cell infusion (day 0), patients received lymphodepleting chemotherapy composing of Fludarabine (30 mg/m2/day) and Cyclophosphamide (250 mg/m2/day) on days -5 to -3. No bridging chemotherapy was given between enrollment and infusion. In CD22 T cell clinical trials, CAR-T cells was given once. All patients underwent bone marrow (BM) biopsy examination and radiology studies on days 30 and every month to determine the response and remission status. Bone biopsy, MRD status by FCM and RT-PCR (if the patient had fusion gene), and EMDs evaluation by CT/MRI/PET-CT were also conducted before CAR T-cell infusion to determine the disease status.

Locations

Country Name City State
China Beijing Boren Hospital Beijing Beijing

Sponsors (1)

Lead Sponsor Collaborator
Beijing Boren Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary CR rate The complete remission(CR) rate to the CAR-T treatment 1 month
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