Patients with leukemia or lymphoma refractory to therapy MedDRA version: 19.0 Level: PT Classification code 10061275 Term: Mantle cell lymphoma System Organ Class: 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps) MedDRA version: 19.0 Level: LLT Classification code 10008957 Term: Chronic lymphatic leukemia System Organ Class: 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps) MedDRA version: 19.0 Level: LLT Classification code 10029473
Conditions
Interventions
Product Name: ARI-0001
Pharmaceutical Form: Solution for infusion
INN or Proposed INN: Adult differentiated autologous T-cells from peripheral blood, expanded and transduced with a lentivirus to expre
Sponsors
IDIBAPS
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Diagnosis of leukemia or CD19 + lymphoma, with a life expectancy less than 2 years that meet the following conditions: Adult acute lymphoid leukemia in second or third response, not candidate for transplantation due to age, associated diseases or lack of donor, or in relapse post allogeneic transplant. Pediatric acute lymphoid leukemia in second or third response, refractory or non-transplant candidate due to donor absence, or in relapse post allogeneic transplant, or with minimal residual residual disease (0.1% or greater) after two or more lines of treatment. Symptomatic follicular lymphoma, which has received at least 2 treatment regimens (one of them including rituximab) and a progression-free interval of less than 2 years. Patients not candidates for transplantation or post-transplant relapse may be included. Symptomatic chronic lymphocytic leukemia, which has received at least 2 treatment regimens (one of them including rituximab) and a progression-free survival of less than 2 years. Patients with a 17p deletion or TP53 mutation may be included after the first line of treatment. Mantle cell lymphoma in the first relapse (or higher) when it is not a candidate for transplantation, or second post-transplant relapse (or higher). Diffuse large cell lymphoma in first relapse (or higher) when it is not a candidate for transplantation, or second post-transplant relapse (or higher). 2. Age greater than 2 years and less than 80. 3. ECOG functional status from 0 to 2 (Annex II). 4. Life expectancy of at least 3 months. 5. Appropriate venous access to perform an apheresis procedure. Absence of contraindications for it. 6. Signature of informed consent (patient or legal guardian). Are the trial subjects under 18? yes Number of subjects for this age range: 10 F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range 10 F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range 10
Exclusion criteria
Exclusion criteria: 1. Treatment with any experimental or non-marketed substance within four weeks prior to recruitment, or actively participating in another therapeutic clinical trial. 2. Diagnosis of another past or present neoplasm. Patients may be included in complete remission for more than 3 years, or with a history of non-melanoma skin cancer or completely resected in-situ carcinoma. 3. Central nervous system involvement (CNS-3) at inclusion. Inclusion will be permitted with patients with a lower grade (CNS-2) or with CNS-3 who have responded to intrathecal chemotherapy. 4. Early relapse after allogeneic transplantation (less than 3 months for apheresis of mononuclear cells, less than 6 months for infusion of ARI-0001) or patients on active immunosuppressive therapy for graft-versus-host disease (corticosteroids or other systemic immunosuppressants ). 5. Active infection requiring systemic medical treatment such as chronic kidney infection, chronic lung infection or tuberculosis. 6. HIV infection. 7. Concurrent and uncontrolled medical illnesses including cardiac, renal, hepatic, gastrointestinal, endocrine, pulmonary, neurological or psychiatric diseases which in the opinion of the researcher represent a risk to the patient. 8. Positive serology for hepatitis B, defined as a positive test for HBsAg. In addition, if the patient is HBsAg negative but has anti-HBc antibodies it will be necessary to perform a DNA test of the hepatitis B virus, and if the result is positive the patient will be excluded. 9. Positive serology for hepatitis C, defined as a positive test for anti-HCV antibodies confirmed by RIBA. 10. Severe organ failure, defined as a cardiac ejection fraction 3 times the upper limit of normal (unless it is due to CLL or Gilbert syndrome). 11. Pregnant or lactating women. Women of childbearing potential should have a negative pregnancy test in the screening phase. 12. Women of childbearing age, including those whose last menstrual cycle was in the year prior to screening, who are unable or unwilling to use highly effective contraceptive methods * from the start of the study to the end of the study. 13. Men who are unable or unwilling to use highly effective contraceptive methods * from the start of the study to the completion of the study. 14. The need to take glucocorticoids in a chronic manner at doses higher than 10 mg / day of prednisone (or equivalent) or other chronic immunosuppressants. * Hormonal contraceptives, intrauterine device, intrauterine systems of hormonal release, sexual abstinence, vasectomy of the couple or bilateral tubal occlusion.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Main Objective: To assess the infusion of ARI-0001 cells (Adult differentiated autologous T-cells from peripheral blood, expanded and transduced with a lentivirus to express a chimeric antigen receptor with anti-CD19 specificity [A3B1] conjugated with the co-stimulatory regions 4-1BB and CD3z ) safety on patients with leukemia or lymphoma CD19+ resistant or refractory to treatment and with a prognosis of less than 2 years.;Secondary Objective: • Evaluate the infusion of ARI-0001 effectiveness • Evaluate the duration of the infusion of ARI-0001 • Evaluate the overall survival after the infusion of ARI-0001 • Evaluate the duration of ARI-0001 cells in peripheral blood, bone marrow and CSF after administration • Evaluate the effect of ARI-0001 treatment on patients quality of life • Assess adverse events occurring at 3 months and at the first year.;Primary end point(s): To assess the infusion of ARI-0001 cells safety on the basis of the following parameters: - Procedure-related mortality (PRM) at the first and third year, defined as any death not caused directly by leukemia / lymphoma. For the estimation of PRM, relapse or progression of the disease will be considered as a competitive event. - Assessment of toxicity at 3 months and first year, defined as number of adverse events grade III-IV using CTC (common toxicity criteria) version 3.0. Particular attention will be paid to cytokine release syndrome, neurological toxicity and the occurrence of second malignancies.;Timepoint(s) of evaluation of this end point: Month 3, year 1 and year 3 | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary end point(s): - Response rate (overall and complete) at 3 months and first year, defined differently for each disease. o On chronic lymphoid and acute lymphocytic leukemia, the usual criteria NCCN and IWCLL will be used. o On non-Hodgkin's lymphoma, the Lugano criteria will be used. o On patients with leukemia will be quantified the persistence of minimal residual disease, in bone marrow and peripheral blood, using multiparametric cytometry and new generation sequencing techniques. - Progression-free survival at 2 years after the procedure, defined as the time lag between infusion of ARI-0001 and the progression of disease or death. Patients alive and in complete remission will be censored at the last follow-up. - Overall survival (OS) at 2 years, defined as the time lag between the infusion of ARI-0001 and the death of the patient from any cause. Living patients will be censored at the the last follow-up. - In vivo survival of ARI-0001 cells in peripheral blood, bone marrow and cerebrospinal fluid, determined, monthly during the first 6 months and thereafter quarterly until the 2 years after infusion, by flow cytometry and quantitative transgene PCR. - Quality of life of included patients, evaluated by a questionnaire completed by patients or their legal guardians at 3 and 6 months and a year after. - Toxicity assessment at 3 months and a year after, defined as number of adverse events of any type occurring throughout the study using the common toxicity criteria (version 3.0);Timepoint(s) of evaluation of this end point: month 3, month 6, 1 year, 2 years and 3 years | — |
Countries
Spain
Contacts
Public ContactJudit Pich Martinez
Hospital Clínic
Outcome results
None listed