T-Cell Acute Lymphoblastic Leukemia/Lymphoblastic Lymphoma
Conditions
Keywords
T-ALL, T-LL, Relapsed, Refractory, anti-CD7 PEBL-CAR T
Brief summary
The main purpose of this study is to evaluate the safety, to establish the recommended dose, and to evaluate the antitumor effect of CD7-CART01 in pediatric patients with relapsed or refractory (R/R) T-cell acute lymphoblastic leukemia (T-ALL) or lymphoblastic lymphoma (T-LL).
Detailed description
This is an in-human, open-lable, single-arm, single-agent, Phase 1/2 study in pediatric patients with R/R T-ALL/T-LL who have failed at least one standard frontline chemotherapy or relapsed after allogeneic hematopoietic stem cell transplantation (HSCT). The study will consist of two phases, Phase 1 and Phase 2. During the Dose Escalation portion of the trial (Phase 1) up to 12 patients will receive CD7-CART01, in up to 2 dose levels until maximum tolerated dose (MTD) is determined. If 2 DLTs are observed in the dose level 1 an additional DL0 will be explored. The dose escalation phase will enroll successive cohorts of 3 up to 6 patients guided by a standard dose-finding 3 + 3 design. Once the recommended phase 2 dose (RP2D) is defined, the phase 2 portion of the study will enroll at the MTD/RD identified in the phase I up to 26 pediatric patients (for both phases) and the study protocol will be amended to include additional, international centers.
Interventions
BIOLOGICALCD7-CART01
A single IV infusion of CD7-CART01 on Day 0
Sponsors
Bambino Gesù Hospital and Research Institute
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
6 Months to 25 Years
Healthy volunteers
No
Inclusion criteria
Procurement eligibility Inclusion Criteria: 1. Diagnosis of CD7 expressing (\> 98% CD7 expression on blast cells) T-ALL or LL and one of the following: 1. Patients in 1st or subsequent relapse, after at least one standard frontline chemotherapy with BM involvement (MRD \>1% in 2 consecutive determinations or evidence of morphological relapse, i.e. \>5% blasts in BM); 2. Relapse after allogeneic HSCT, if at least 100 days post-transplant, if there is no evidence of active GVHD and if the patient is no longer taking immunosuppressive agents for at least 30 days prior to enrollment; 3. CNS disease as defined as \> 5 WBCs/mcL in CSF with morphological/flow-cytometry evidence of blasts or biopsy proven recurrence in the eye or brain; 4. Extramedullary relapse as defined by morphological evidence of blasts in the testis or any other extramedullary sites; 5. Refractory disease, defined as MRD ≥ 1% or \<1% but persistently positive (i.e. a positive MRD value confirmed by PCR at 2 subsequent evaluations performed at least 2 weeks apart), at the end of consolidation blocks in newly diagnosed patients; 2. Age: 6 months - 25 years. 3. Adequate venous access for apheresis or eligible for appropriate catheter placement, and no other contraindications for leukapheresis. 4. Voluntary informed consent is given. For subjects \<18-year-old, or below the age required by each Country regulation, their legal guardian must give informed consent. Pediatric subjects will be included in age-appropriate discussion and verbal assent will be obtained for those greater than or equal to 12 years of age, when appropriate, or to sign age-adapted informed consent, according to the regulatory requirement of each Country. 5. Clinical performance status: Patients \> 16 years of age: Karnofsky greater than or equal to 60%; Patients \< 16 years of age: Lansky scale greater than or equal to 60%.
Exclusion criteria
1. Severe, uncontrolled active intercurrent infections. 2. HIV, or active HCV and/or HBV infection. 3. Blast contamination in peripheral blood \>5%, by flow-cytometry, at the time of leukapheresis collection. 4. Concurrent or recent prior therapies, before apheresis: 1. Systemic steroids (at a dose equivalent to or greater than 2 mg/kg prednisone) in the 2 weeks before apheresis collection. Recent or current use of inhaled/topical/non-absorbable steroids is not exclusionary 2. Systemic chemotherapy in the 2 weeks preceding apheresis collection 3. Nelarabine, daratumomab, clofarabine exposure in the 3 weeks preceding apheresis collection 4. Anti-thymocyte globulin (ATG) or Alemtuzumab (Campath®) in the 8 weeks preceding apheresis collection 5. Immunosuppressive agents in the 2 weeks preceding apheresis collection 6. Radiation therapy must have been completed at least 2 weeks prior to apheresis 7. Other anti-neoplastic investigational agents currently administered or within 30 days prior to apheresis (i.e. start of protocol therapy) 8. Exceptions: * There is no time restriction with regard to prior intrathecal chemotherapy, provided that there is complete recovery from any acute toxic effects of such chemotherapy; * Patients who relapse while receiving standard ALL maintenance chemotherapy will not be required to have a waiting period before entry onto this study provided they meet all other eligibility criteria; * Subjects receiving steroid therapy at physiologic replacement doses only are allowed provided there has been no increase in dose for at least 2 weeks prior to starting apheresis. Treatment eligibility Inclusion criteria: 1. Diagnosis of CD7 expressing (\> 98% CD7 expression on blast cells) T-ALL or LL and one of the following: 1. Patients in 1st or subsequent relapse, after at least one standard frontline chemotherapy with BM involvement (MRD \>1% in 2 consecutive determinations or evidence of morphological relapse, i.e. \>5% blasts in BM) 2. Relapse after allogeneic HSCT, if at least 100 days post-transplant, if there is no evidence of active GVHD and if the patient is no longer taking immunosuppressive agents for at least 30 days prior to enrollment 3. CNS disease as defined as \> 5 WBCs/mcL in CSF with morphological or flow-cytometry evidence of blasts or biopsy proven recurrence in the eye or brain 4. Extramedullary relapse as defined by morphological evidence of blasts in the testis or any other extramedullary sites 5. Refractory disease, defined as MRD ≥1% or \<1% but persistently positive (i.e. a positive MRD value confirmed by PCR at 2 subsequent evaluations performed at least 2 weeks apart), at the end of consolidation blocks in newly diagnosed patients 2. Measurable or evaluable disease at the time of enrollment, which may include any evidence of disease, including MRD detected by flow-cytometry, cytogenetics, or polymerase chain reaction (PCR) analysis. 3. Age: 6 months - 25 years. 4. Before enrollment for treatment, patients must have a potential allogeneic hematopoietic stem cell (HSC) donor (matched related, matched unrelated or haploidentical) available. 5. Voluntary informed consent is given. For subjects \<18-year-old, or below the age required according to each Country regulation, their legal guardian must give informed consent. Pediatric subjects will be included in age-appropriate discussion and verbal assent will be obtained for those greater than or equal to 12 years of age, when appropriate, or to sign age-adapted informed consent, according to the regulatory requirement of the Country. 6. Clinical performance status: Patients \> 16 years of age: Karnofsky greater than or equal to 60%; Patients \< 16 years of age: Lansky scale greater than or equal to 60%.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Safety (Phase I) and definition of the recommended dose (Phase I) | 28 days | To evaluate the safety of the infusion of CD7-CART01, explore the dose-limiting toxicities (DLT) of the cellular product and define the recommended dose of CD7-CART01, defined as the maximum tolerated dose/recommended dose (MTD/RD), to be evaluated for efficacy in the phase II extension |
| Antitumor effect of CD7-CART01 (Phase II) | 28 days | To evaluate the portion of patients achieving either BM, PB and CSF morphological complete remission (CR) or CR with incomplete blood count recovery (CRi) and with minimal residual disease (MRD) negativity at day 28 |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| In vivo persistence of CD7-CART01 (Phase I and II) | 3 years | To assess the in vivo persistence of the infused T cells using immunoassays and transgene detection (flow-cytometry and Real Time qPCR) |
| Relative proportion and phenotype of CD3+CAR+ T cells/CD3+CAR- T cells/NK cells (Phase I and II) | 3 years | To assess the relative proportion and phenotype of CD3+CAR+ T cells/CD3+CAR- T cells/NK cells at day +28 and whenever it will be the case at subsequent time points |
| Number of participants with treatment-related adverse events as assessed by CTCAE v5.0 | 28 days | In the phase II portion of the study, the treatment-related adverse events will be recorded |
| Assessment of cumulative incidence of overall survival | 3 years | To assess the cumulative incidence of overall survival at 1 and 3 years post cell infusion |
| Assessment of cumulative incidence of disease-free survival | 3 years | To assess the cumulative incidence of disease-free survival at 1 and 3 years post cell infusion |
| Assessment of cumulative incidence of relapse | 3 years | To assess the cumulative incidence of both molecular and morphological relapse (defined as an MRD \>10\^-4 and a BM blast percentage \> 5%, respectively) |
| Antitumor effect of CD7-CART01 (Phase I and II) | 28 days | To assess the Overall Response Rate (ORR) at day 28 |
Countries
Italy
Contacts
Primary ContactFranco Locatelli, MD, PhD
Backup ContactFrancesca Del Bufalo, MD, PhD
Outcome results
None listed