Acute Myeloid Leukaemia (AML), Myelodysplastic Syndromes (MDS)
Conditions
Keywords
Gene Therapy, WT1 TCR, Gene modified T cels
Brief summary
This is a Phase I/II trial to determine safety, clinical efficacy and feasibility of a gene-modified WT1 TCR therapy in patients with myelodysplastic syndrome (MDS) and acute myeloid leukaemia (AML). Patient's white blood cells (T cells) will be modified by transferring a gene which enables them to make a new T cell receptor (TCR) that can recognize fragments of a protein called WT1 (Wilms' tumour 1) which is present at abnormally high levels on the surface of myelodysplastic and leukaemic cells. In this trial, approximately 25 participants with an Human Leukocyte Antigen A2 (HLA-A\*0201) tissue type who have failed to achieve or maintain an IWG defined response following hypomethylating agent therapy will be recruited.
Detailed description
This is a Phase I/II trial to determine safety, clinical efficacy and feasibility of a gene-modified WT1 TCR therapy. Following provision of informed consent, each subject will undergo screening assessments, including HLA-A\*0201 screening (if not already documented) and a bone marrow aspirate/biopsy (BMA) to determine subject eligibility for the trial. Subjects will undergo leukapheresis within 14 days of screening. Once successful manufacture of the WT1 TCR-transduced T cells has been confirmed by the Sponsor, each subject will be administered a lymphodepletive conditioning regimen for five days consisting of fludarabine x 5 days 30mg/m2 intravenous (i.v.) and methylprednisolone x 1 day 500 mg i.v. Upon completion of the conditioning regimen, subjects will receive an infusion of WT1 TCR-transduced T cells of ≤2 x 107/kg, followed by daily IL-2 subcutaneous injections (1 x 106 units/m2 subcutaneous (s.c.) od) for 5 days. If an IWG response has not been reported (one or more criteria met) at 3 months post-infusion then, if agreed by both the Investigator and Sponsor, the subject will be offered to have a repeat infusion of WT1 TCR-transduced T cells. Following infusion, subjects will enter an intensive period of out-patient follow-up to observe them for any acute complications and toxicities. Subjects will then be followed monthly in the clinic for the first 6 months for routine safety and clinical evaluations, including disease response evaluations. All subjects will be followed-up for a minimum of 12 months.
Interventions
GENETICAutologous WT1 TCR transduced T cells
Gene therapy: Autologous WT1 TCR transduced T cells administered by intravenous infusion
Sponsors
University College, London
Cell Therapy Catapult
Cell Medica Ltd
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
Key Inclusion criteria: * The trial will recruit subjects with MDS or AML who have received hypomethylating agent therapy (at least 6 cycles of azacitidine or 4 cycles of decitabine), and are EITHER: * Relapsed, defined as failing to maintain an initial IWG response OR • Stable, defined as failing to achieve an IWG response Subjects who have received hypomethylating agent therapy as part of a combination regimen may be eligible after discussion with the Sponsor. 1. Subjects aged 18 years or older who have a diagnosis of, EITHER: * MDS with an IPSS of intermediate -2, or high and one of the following FAB types: * Refractory anaemia with excess blasts (RAEB) * Chronic myelomonocytic leukaemia (CMML) with at least 10% bone marrow blasts (WHO CMML II) OR * AML (diagnosed according to WHO classification 2008 revision) 2. Subjects with documented HLA-A\*0201 positive serotype 3. Subjects with less than 30 per cent bone marrow blasts 4. Subjects with relapsed disease must have less than 5 per cent peripheral blasts 5. Subjects with stable disease must have less than 10 per cent peripheral blasts 6. Subjects with less than a doubling of bone marrow blast count between the start of hypomethylating agent therapy and the date of screening 7. Subjects to complete screen 1 visit within a minimum of 28 days and maximum of 90 days since completion of azacitidine or decitabine therapy. Subjects who have exceeded the 90 day window may be eligible after discussion with the Sponsor. 8. Subjects with ECOG status 0, 1 or 2 9. Subjects who have at least one cytopenia (ANC \<1000/μL, platelet count \<75,000/μL, Hgb \<11g/dL or RBC transfusion dependence) Key
Exclusion criteria
improvement or molecular response following azacitidine treatment * CMML patients who have a white blood cell count \> 13 x 109/L * Acute promyelocytic leukaemia (FAB M3 Classification) * Uncontrolled intercurrent illness * Active malignancy, except basal cell or squamous cell skin cancer or carcinoma in situ of the cervix or breast * Known history of Human Immunodeficiency Virus (HIV), Hepatitis C virus (HCV) or Hepatitis B virus (HBV) or positive for Human T-Lymphocyte Virus (HTLV) or Syphilis. • Active auto-immune disease * Clinically significant non-hematologic toxicity after prior therapy chemotherapy higher than grade 1 per Common Terminology Criteria for Adverse Events (CTCAE) (v 4.0) * Subjects who require haemodialysis or peritoneal dialysis * Pregnant and lactating women * Subjects unwilling or unable to use adequate contraceptive precautions at screening and throughout the trial * Subjects who have undergone major surgery without full recovery within last 28 days prior to screening * Subjects with known hypersensitivity to cyclophosphamide, fludarabine, methylprednisolone or IL-2 (Interleukin-2)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Proportion of subjects achieving one or more IWG response criteria following gene-modified WT1 TCR T cell therapy | 12 Months |
| Safety following gene-modified WT1 TCR T cell therapy as measured by suspected unexpected serious adverse reactions (SUSARS) | 12 Months |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Technical feasibility of gene-modified WT1 TCR therapy in subjects with Myelodysplastic Syndrome (MDS) or Acute Myeloid Leukaemia (AML). | 12 Months | — |
| Persistence of WT1 TCR-transduced T cells | 12 Months | Persistence of infused WT1 TCR-transduced T cells by Vβ2.1 and tetramer staining and PCR for Vβ2.1 and TCR-vector fragments. |
| Safety and tolerability of gene-modified WT1 TCR therapy as measured by clinical laboratory parameters and adverse events | 12 Months | — |
| WT1 Transcript analysis in AML/MDS cells | 12 Months | WT1 overexpression will be used as a measure of disease monitoring on peripheral blood and BMA samples. RT-qPCR will be used to detect WT1 transcripts. |
| Functionality and phenotype of WT1 TCR-transduced T cells | 12 Months | Function will be evaluated by measuring antigen-specific intracellular cytokine production in response to target cells that express HLA-A\*201 alleles as well as WT1. Surface differentiation and memory phenotype will be determined using multi-parameter flow cytometry. |
| Efficacy of WT1 TCR therapy as measured by haematological improvement, overall remission rate, marrow remission, cytogenetic response, molecular response, stable disease, AML transformation, progression free, event free and overall survival | 12 Months | Haematologic Response (peripheral blood): Haematological response will be assessed by haematology results and capturing data on number of RBC/platelet transfusions given to the subject. Marrow Response: Bone marrow aspirate and/or biopsy morphology results will be recorded and assessed for marrow response in combination with peripheral blood response Cytogenetic response: cytogenetic evaluations will be performed on bone marrow aspirates/biopsies obtained during the trial. Molecular response: molecular profile evaluations will be performed on bone marrow aspirates/biopsies obtained during the trial. Disease response: Investigator will determine response (CR, PR, stable disease (SD), PD/TF) to administration of WT1 transduced T cells based on bone marrow blast count and peripheral blood assessments. Subject disease events, progression and survival will be reviewed, assessed and recorded by the Investigator. |
Countries
Belgium, Germany, United Kingdom
Outcome results
None listed