Acute Lymphoblastic Leukemia ,Lymphomas Clinical Trial
Official title:
Study Evaluating the Safety and Efficacy With Anti-CD19 CAR-T Cells for Relapsed or Refractory Acute Lymphoblastic Leukemia and Lymphomas
This is a single arm, open-label, single center study to determine the safety and efficacy of Anti-CD19 CAR-T cells in patients with relapsed or refractory acute lymphoblastic leukemia and Lymphomas.
| Status | Recruiting |
| Enrollment | 20 |
| Est. completion date | August 1, 2021 |
| Est. primary completion date | August 1, 2020 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years to 70 Years |
| Eligibility |
Inclusion Criteria: Subjects diagnosed as Relapsed or Refractory acute lymphoblastic
leukemia and Lymphomas ,and have no effective treatment option (such as autograft or
allogeneic stem cell transplantation) and estimated survival time of the current treatment
< 2 years, The specific requirements are as follows: 1. Male or female aged 18-70 years old ; 2. Estimated Survival time > 12 weeks; 3. Relapsed and refractory acute lymphoblastic leukemia and lymphoma were confirmed by physical examination, pathological examination, laboratory examination and imaging; 4. Chemotherapy failure or recurrent acute lymphoblastic leukemia and Lymphomas; 5. Glutamic-pyruvic transaminase, glutamic oxalacetic transaminase< 3 fold of normal level; 6. Bilirubin<2.0mg/dl; 7. Karnofsky Performance Status>50% at the time of screening; 8. Adequate pulmonary, renal, hepatic, and cardiac function; 9. Fail in autologous or allogenic haemopoietic stem cell transplantation; 10. Not suitable for stem cell transplantation conditions or abandoned due to conditions; 11. Free of leukocytes removal contraindications; 12. Voluntarily join CAR-T clinical trial ,Understand and sign written informed consent. Exclusion Criteria: 1. The patient is a pregnant or breastfeeding woman, or is a woman with a pregnancy plan within six months; 2. Patients have infectious diseases (such as HIV, active tuberculosis, etc.); 3. The patient is an active hepatitis B or hepatitis C infection; 4. Feasibility assessment proves that the efficiency of transduction of lymphocyte is below 10% or the lymphocyte cannot be propagated ; 5. Abnormal vital signs; 6. Subjects with mental or psychological illness who cannot be combined with treatment and efficacy evaluation; 7. Highly allergic constitution or history of severe allergies, especially allergy to interleukin-2; 8. General infection or local severe infection, or other infection that is not controlled; 9. Dysfunction in lung, heart, kidney and brain; 10. Severe autoimmune diseases; 11. Other symptoms that are not applicable for CAR-T. |
| Country | Name | City | State |
|---|---|---|---|
| China | The First Affiliated Hospital of Nangchang University | Nanchang | Jiangxi |
| Lead Sponsor | Collaborator |
|---|---|
| The First Affiliated Hospital of Nanchang University |
China,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Overall responce rate(ORR) | Assessment of ORR (ORR = CR+PR ) at 2 months of treatment | 2 years | |
| Primary | Overall survival (OS) | Assessment of OS(Overall survival) at 6 months of treatment | 2 years | |
| Primary | Progression-free survival (PFS) | Assessment of PFS(Progression-free survival ) at 6 months of treatment | 2 years | |
| Primary | minimal residual disease(MRD) | Assessment of MRD negative overall response rate at 3 months of treatment | 2 years | |
| Secondary | Safety (incidence of adverse events defined as dose-limited toxicity) | Occurrence of study related adverse events defined as NCI CTCAE 4.0 > grade 3 possibly, probably, or definitely related to study treatment. | Study treatment until Week 24 | |
| Secondary | Expression of CD19 CART cells | Expression of CD19 CART cells detected by flow cytometry in blood and bone marrow. | 2 years | |
| Secondary | Detection of CD19 CART cells | Detection of CD19 CART cells in blood, bone marrow by Quantitative Polymerase Chain Reaction (q-PCR). | 2 years |