Anti-CD33 CAR NK Cells in the Treatment of Relapsed/Refractory Acute Myeloid Leukemia

Leukemia, Myeloid, Acute Clinical Trial

Official title:

Phase I Study to Evaluate the Safety and Effectiveness of Anti-CD33 CAR NK Cell Therapy in Relapsed/Refractory Acute Myeloid Leukemia

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05008575
• Other study ID #: CD33 CAR NK-AML
• Status: Recruiting
• Phase: Phase 1
• Start date: December 23, 2021
• Est. completion date: December 1, 2023

Study information

• Verified date: December 2021
• Source: Xinqiao Hospital of Chongqing
• Contact: Xi zhang, MD/PhD
• Phone: 13808310064
• Email: zhangxxi[@]sina.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

CAR technology has been used in T cell therapy and gets great success in treating hematological diseases. Following models of CAR T cells, CAR NK cell therapy has been one hot point. For myeloid malignancies, CD33 is widely expressed. Targeting CD33 surface antigens by CAR NK cells provides an off-the-shelf immune cell therapy.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 27
• Est. completion date: December 1, 2023
• Est. primary completion date: December 1, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

1. ECOG performance status score = 2.

2. Life expectancy = 12 weeks from the time of enrollment.

3. Disease status at the time of enrollment: -Patients with AML (except M3) who have not achieved complete remission after standard chemotherapy regimens; -Not suitable or unconditional for allogeneic hematopoietic stem cell transplantation; -Patients with recurrent acute myeloid leukemia after autologous hematopoietic stem cell transplantation without active graft-versus-host disease (GVHD).

4. CD33 expression must be detected on greater than 50% of the malignant cells by immunohistochemistry or greater than 80% by flow cytometry.

5. Adequate main organ function as assessed by the following laboratory requirements:

creatinine = 2.5 × upper limit of normal, cardiac ejection fraction = 40%, oxygen saturation = 90%, total bilirubin = 3 × upper limit of normal, aspartate aminotransferase (AST) and alanine aminotransferase (ALT) = 3 × upper limit of normal, Hgb=80g/L.

6. Without history of accepting anti-cancer therapy, including chemotherapy, radiotherapy, immunotherapy (immune suppressive drugs or corticosteroid treatment) within 4 weeks of screening.

7. Women of child-bearing age must have evidence of negative pregnancy test.

8. Subjects of reproductive potential must agree to use acceptable birth control methods within 1 year after treatment, as described in protocol.

9. After discussion by the expert group, the patient's condition was analyzed and combined with the general physical condition of the patient, the benefit of participating in the clinical trial was greater than the risk.

10. All participants must have the ability to understand and willingness to sign a written informed consent.

Exclusion Criteria:

1. Diagnosis of acute promyelocytic leukemia (APL M3): t(15;17)(q22;q12); (promyelocytic leukemia [PML]/retinoic acid receptor [RAR] alpha [a]) and variants excluded.

2. Active acute or chronic GVHD or requirement of immunosuppressant medications for GVHD within 4 weeks of enrollment.

3. Have been diagnosed with or treated other malignant tumors other than AML within 5 years before screening, except for the following conditions: participants with adequately treated cervical carcinoma in situ, basal cell or squamous cell skin cancer; or received radical treatment Local prostate cancer, ductal carcinoma in situ.

4. There are serious systemic diseases: New York Heart Association (NYHA) stage III or IV congestive heart failure; cerebrovascular accident or myocardial infarction or hemodynamic instability caused by arrhythmia within 6 months before signing the informed consent; impaired cardiac function (LVEF<50%) assessed by echocardiographic scan.

5. Sever illness or medical condition, which would not permit the patient to be managed according to the protocol, including active uncontrolled infection.

6. Pregnant or lactating women.

7. Subjects with radiologically-detected CNS chloromas or CNS 3 disease (presence of = 5/µL white blood cells (WBCs) in cerebral spinal fluid (CSF) and cytospin positive for blasts [in the absence of a traumatic lumbar puncture] and/or clinical signs of CNS leukemia such as a cranial nerve palsy from active disease). Subjects with adequately treated CNS leukemia are eligible.

8. Human immunodeficiency virus (HIV) seropositivity; hepatitis B surface antigen is positive or HBV DNA is higher than the detection limit of the analysis method; hepatitis C antibody is positive or HCV RNA is higher than the detection limit of the analysis method; syphilis antibody and syphilis rapid plasma reagin are positive; CMV DNA is positive.

9. Patients who suffer from allergies for any cytokines or antibodies.

10. Contraindications for fludarabine or cyclophosphamide treatment.

11. Receiving corticosteroids at >20 mg daily prednisone dose or equivalent.

12. Drug abuse and addiction.

13. History of mental disorders.

14. Other patients that researchers considered unsuitable for inclusion.

Related Conditions & MeSH terms

• Leukemia
• Leukemia, Myeloid
• Leukemia, Myeloid, Acute

Intervention

Biological:
• anti-CD33 CAR NK cells
6×10^8, 12×10^8, 18×10^8/KG Treatment follows a lymphodepletion

Drug:
• Fludarabine
recommendation: 30mg/m2 (D-5~D-3),determined by tumor burden at baseline.
• Cytoxan
recommendation: 300-500mg/m2 (D-5~D-3),determined by tumor burden at baseline.

Locations

Country	Name	City	State
China	Department of Hematology, Xinqiao Hospital	Chongqing	Chongqing

Sponsors (2)

Lead Sponsor	Collaborator
Xinqiao Hospital of Chongqing	Sichuan Kelun-Biotech Biopharmaceutical Co., Ltd.

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Overall Remission Rate (ORR)	Assessment of morphologic complete remission (CR), complete remission with incomplete recovery of counts (CRi), no residual disease as analyzed by flow cytometry analysis, and molecular remission by molecular studies	4 weeks after infusion
Primary	incidence of participants with dose limiting toxicity (DLT)	To characterize the safety, tolerability of Anti-CD33 CAR NK cells	within 4 weeks after infusion
Secondary	Progression-free survival (PFS)		up to 2 years after infusion
Secondary	Overall Response Rate (ORR)		up to 2 years after infusion
Secondary	Overall survival(OS)		up to 2 years after infusion