Administration of Autologous CAR-T Cells Targeting the CD19 Antigen and Containing the Inducible caspase9 Safety Switch in Patients With Relapsed/Refractory Acute Lymphoblastic Leukemia

Description

The body has different ways of fighting infection and disease. No single way is effective at fighting cancer. This research study combines two different ways of fighting disease: antibodies and T cells. Antibodies are proteins that protect the body from disease caused by bacteria or toxic substances. Antibodies work by binding those bacteria or substances, which stops them from growing and causing bad effects. T cells, also called T lymphocytes, are special infection-fighting blood cells that can kill other cells, including tumor cells or cells that are infected. Both antibodies and T cells have been used to treat patients with cancers. They both have shown promise, but neither alone has been sufficient to cure most patients. This study combines both T cells and antibodies to try to create a more effective treatment. This investigational treatment is called autologous T lymphocyte chimeric antigen receptor cells targeted against the CD19 antigen (ATLCAR.CD19) administration. In previo

Trial Eligibility

All clinical and laboratory data required for determining eligibility must be available in the subject's medical/research record which will serve as the source document. Subjects may be transfused with blood products to obtain a hemoglobin level \> 7.0 g/dL and platelet count \> 20,000 per μl. Note: During the period after cell procurement and during iC9-CAR19 T-cell production, subjects are allowed to receive standard of care intervening therapy for ALL to manage their disease if the treating physician feels it is in the subject's best interest Common Inclusion Criteria for all subjects * Written informed consent for procurement signed by subject or legal guardian of a pediatric subject and HIPAA authorization * Age 3 to 17 years of age for pediatric subjects (weight must be ≥10 kg), ≥ 18 to 70 years of age for adults at the time of consent. * Karnofsky score \> 60%, if ≥16 years old, or Lansky performance score of greater than 60% if \<16 years old . Demonstrate adequate renal and hepatic function as defined below; all screening labs to be obtained within 72 hours prior: System Laboratory Value Renal\* Serum Creatinine (sCr) ≤ 1.5 × ULN) Hepatic: Total bilirubin (tBili) ≤ 1.5 × ULN, unless attributed to Gilbert's Syndrome Aspartate aminotransferase (AST) ≤ 3.0 × ULN Alanine aminotransferase (ALT) ≤ 3.0 × ULN * Females of childbearing potential must have a negative serum pregnancy test within 72 hours prior to procurement. Note: Females are considered of childbearing potential unless they are premenarchal, surgically sterile (have undergone a hysterectomy, bilateral tubal ligation, or bilateral oophorectomy) or they are naturally postmenopausal for at least 12 consecutive months. * Females and males of childbearing potential must be willing to abstain from heterosexual activity or to use two forms of effective methods of contraception from the time of informed consent until 3 months after treatment discontinuation. The two contraception methods can be comprised of two barrier methods, or a barrier method plus a hormonal method. Female participants will inform their male partners that they must use the methods of birth control required by the protocol. * Male subjects with female partners must have had a prior vasectomy or agree to use an adequate method of contraception (i.e., double barrier method: condom plus spermicidal agent) starting with the first dose of study therapy through 3 months after the last dose of study therapy. As determined by the enrolling physician or protocol designee, ability of the subject to understand and comply with study procedures. Inclusion Criteria for Cell Procurement * Relapsed or refractory precursor B cell ALL: * 2nd or greater bone marrow or central nervous system (CNS) relapse, * Any bone marrow or CNS relapse \>100 days after allogeneic stem cell transplant, Primary refractory ALL defined as no complete response after 2 cycles of a standard of care chemotherapy regimen, or * For adult subjects: first bone marrow or CNS relapse with duration of first CR \<1 year, or CR1 duration ≥1 year and refractory to ≥1 cycle of therapy for treatment of relapse * Subjects with isolated non-CNS extramedullary disease will be eligible as long as the time-of-remission criteria above for bone marrow and CNS relapses or primary refractory ALL are met and the biopsy for extramedullary disease confirms CD19 expression * For pediatric subjects: first bone marrow, CNS or isolated non-CNS extramedullary relapse refractory to more than 1 cycle of standard therapy for relapsed ALL * While active CNS3 leukemia will be excluded, subjects with concurrent CNS3 disease and bone marrow relapse who have responded to CNS-directed therapy prior to enrollment will be allowed to participate. Intrathecal chemotherapy will be allowed to continue between lymphodepleting chemotherapy and cell infusion. * Subjects with CNS2 disease and concurrent bone marrow relapse will be eligible. Intrathecal chemotherapy will be allowed to continue between lymphodepleting chemotherapy and cell infusion * Subjects who have previously achieved remission with no detectible measurable residual disease (MRD) by multi-parameter flow cytometry, and who have re- developed CD19+ MRD measured by multi-parameter flow cytometry will be eligible, provided that the duration of first MRD-negative CR was \<1 year, MRD- negative CR1 duration ≥1 year and refractory to ≥1 cycle of therapy for treatment of MRD recurrence, or MRD reappearance occurs during second or subsequent CR. * Subjects who have persistent CD19+ MRD measured by multi-parameter flow cytometry after 3 cycles of initial chemotherapy, and have persistence of CD19+ MRD after one or more cycles of blinatumomab. * Subjects with Ph+ ALL will be eligible if they have failed ≥ 2 ABL tyrosine kinase inhibitors, relapsed after allogeneic stem cell transplant or have CD19+ MRD. Subjects with the T315I ABL kinase point mutation will be eligible if they have failed ponatinib-containing therapy, regardless of the number of prior ABL tyrosine kinase inhibitors. * CD19 positivity of lymphoblasts confirmed by flow cytometry or IHC per institutional standards. * Life expectancy ≥ 12 weeks. * Demonstrate adequate renal and hepatic function as defined below; all screening labs to be obtained within 72 hours prior to procurement. \*For pediatric patients, adequate renal function is defined as below: Age Maximum Serum Creatinine (mg/dL) Both (Male, Female) 3 to \<6 years ≤0.8 6 to \<10 years ≤1 10 to \<13 years ≤1.2 13 to \<16 years (Male) ≤1.5 / Female ≤1.4 16 to \<18 years (Male) ≤1.7 / Female ≤1.4 * Subjects currently receiving "maintenance" doses of chemotherapy are eligible and the need for intrathecal prophylaxis prior to procurement is left to the discretion of the investigator. Maintenance doses of systemic chemotherapy are defined as methotrexate ≤30 mg/m2/week, mercaptopurine ≤100 mg/m2/day and vincristine ≤ 2 mg/28 days. Maintenance therapy in patients with Ph+ leukemia may also contain tyrosine kinase inhibitors (TKIs) targeting BCR-ABL, at the discretion of the investigator. Corticosteroid- containing maintenance therapy is permitted only if corticosteroids are administered \>14 days prior to procurement. Exclusion Criteria for Cell Procurement Subjects meeting any of the following criteria cannot be enrolled in this study: * Subjects with relapsed fulminant CD19+ ALL that is rapidly progressing with circulating lymphoblasts that are rising in proportion to \>50% of circulating white blood cells. * Intrathecal chemotherapy will be allowed to continue between cell procurement and lymphodepleting chemotherapy. * Pregnant or breastfeeding (Note: breast milk cannot be stored for future use if the milk is collected while the mother is being treated on study). * Has a known additional malignancy that is active and/or progressive requiring treatment; exceptions include basal cell or squamous cell skin cancer, in situ cervical or bladder cancer, or other cancer for which the subject has been disease-free for at least five years. * Subjects must not have tumor in a location where enlargement could cause airway obstruction. * Subjects may not have an oxygen requirement as defined by pulse oximetry of \<90% on room air. * Subjects must not have left ventricular ejection fraction of \<40% (shortening fraction \<27% for pediatric subjects) as measured by echocardiogram or MUGA. * Patients with the following systemic viral infections will be excluded: active HIV, HBV, HCV. Only subjects meeting the criteria as so described will be infused. Note: To meet eligibility subjects are required to be negative for HIV antibody or HIV viral load, negative for Hepatitis B surface antigen, or negative for HCV antibody or HCV viral load. * Patients who are on treatment for other active uncontrolled infections (not referenced above) with resolution of signs/symptoms are not excluded. Non-influenza, non-RSV, isolated upper respiratory infections are not excluded. Other active uncontrolled infections will be excluded. * Prior to procurement current use of systemic corticosteroids at doses ≥10 mg/day prednisone or its equivalent; those receiving \<10 mg/day may be enrolled at discretion of investigator. (Note: Corticosteroid use with doses at the discretion of the treating physician are allowed after procurement up to the beginning of lymphodepletion. Corticosteroid use is contraindicated following iC9-CAR19 infusion unless medically necessary e.g., to treat CRS). * Physiologic replacement with hydrocortisone is allowed at doses 6-12 mg/m2/day, or equivalent. * Received anti-CD19 antibody-based therapy or cytotoxic chemotherapy not described as maintenance therapy (within 2 weeks of procurement per section). Inclusion Criteria for Lymphodepletion: * Relapsed or refractory precursor B cell ALL, confirmed by presence of blasts in the blood or bone marrow (≥5%) or in any extramedullary site. Subjects who have previously achieved remission with no detectible measurable residual disease (MRD) by multi- parameter flow cytometry, and who have re-developed CD19+ MRD measured by multi- parameter flow cytometry are eligible, provided that the duration of first MRD-negative CR was \<1 year, MRD-negative CR1 duration ≥1 year and refractory to ≥1 cycle of therapy for treatment of MRD recurrence/relapse, or MRD-recurrence in second or subsequent morphologic CR. Additionally, subjects who have persistent CD19+ MRD measured by multi-parameter flow cytometry after 3 cycles of initial chemotherapy, and have persistence of CD19+ MRD after one or more cycles of blinatumomab are eligible to participate. Because CNS leukemia is not curable with conventional therapies, subjects who met inclusion criterion for CNS leukemia at the time of procurement will be eligible for lymphodepletion even if intrathecal or systemic chemotherapy has rendered their cerebrospinal fluid free of lymphoblasts prior to lymphodepletion. * Life expectancy ≥ 12 weeks. * Subjects who have received prior therapy with murine antibodies must have documentation of absence of human anti-mouse antibodies (HAMA) prior to lymphodepletion on this study. Demonstrate adequate renal and hepatic function as defined below; all screening labs to be obtained within 72 hours prior to lymphodepletion. * For pediatric patients, adequate renal function is defined as below: Age Maximum Serum Creatinine (mg/dL) Both Male/Female 3 to \<6 years ≤0.8 6 to \<10 years ≤1 10 to \<13 years ≤1.2 13 to \<16 years (Male) ≤1.5/ (Female) ≤1.4 16 to \<18 years (Male) ≤1.7/(Female) ≤1.4 * As determined by the enrolling physician or protocol designee, ability of the subject to understand and comply with study procedures. * For subjects who receive chemotherapy between cell procurement and lymphodepletion, washout periods as described in exclusion criteria sections 4.4.5 to 4.4.11 between chemotherapy and the beginning of lymphodepletion will be required. * Subjects must have autologous transduced activated T cells that meet the Certificate of Analysis (CofA) acceptance criteria. Exclusion Criteria for Lymphodepletion Subjects meeting any of the following criteria cannot be enrolled in this study: * Pregnant or breastfeeding (Note: breast milk cannot be stored for future use if the milk is collected while the mother is being treated on study). * Has a known additional malignancy that is active and/or progressive requiring treatment; exceptions include basal cell or squamous cell skin cancer, in situ cervical or bladder cancer, or other cancer for which the subject has been disease-free for at least five years. * Subjects must not have tumor in a location where enlargement could cause airway obstruction. * Subjects may not have an oxygen requirement as defined by pulse oximetry of \<90% on room air. * Treatment with any investigational drug within 14 days (i.e., two weeks) prior to lymphodepletion or has received any tumor vaccines within the previous five weeks prior to lymphodepletion. * Subject has received pegylated-asparaginase ≤3 weeks prior to lymphodepletion. * Radiotherapy to a non-CNS site completed \<1 week prior to lymphodepletion, or CNS directed radiation completed \<7 weeks prior to lymphodepletion. * Subject is receiving following drugs \<1 week prior to lymphodepletion: salvage chemotherapy (e.g. clofarabine, cytosine arabinoside \> 100 mg/m2, anthracyclines, cyclophosphamide, methotrexate ≥ 25 mg/m2).. * Any systemic drug used for GVHD must be stopped \>3 weeks prior to lymphodepletion (e.g. calcineurin inhibitors, methotrexate or other chemotherapy drugs, mycophenolyate, rapamycin, thalidomide, or immunosuppressive antibodies such as anti-CD20 (rituximab), anti-TNF, anti-IL6 or anti-IL6R, systemic steroids). * The following drugs must be stopped prior to the beginning of lymphodepleting chemotherapy: tyrosine kinase inhibitors, hydroxyurea, vincristine, 6-mercaptopurine, 6- thioguanine, methotrexate \<25 mg/m2, cytosine arabinoside \<100 mg/m2/day, and asparaginase (non-pegylated). These drugs should not be administered concomitantly or following lymphodepleting chemotherapy . * CNS prophylaxis or treatment of CNS leukemia with intrathecal methotrexate, cytarabine and/or hydrocortisone treatment must be stopped prior to lymphodepleting chemotherapy. * Patients with the following systemic viral infections will be excluded: active HIV, HTLV, HBV, HCV. Note: To meet eligibility subjects are required to be negative for HIV antibody or HIV viral load, negative for Hepatitis B surface antigen, or negative for HCV antibody or HCV viral load. * Patients who are on treatment for other active uncontrolled infections (not referenced above) with resolution of signs/symptoms are not excluded. Non-influenza, non-RSV, isolated upper respiratory infections are not excluded. Other active uncontrolled infections will be excluded. * Use of systemic corticosteroids at doses ≥10 mg/day prednisone or its equivalent; those receiving \<10 mg/day may be enrolled at discretion of investigator. (Note: Corticosteroid use with doses at the discretion of the treating physician are allowed after procurement up to the beginning of lymphodepletion.). Physiologic replacement with hydrocortisone is allowed at 6-12 mg/m2/day, or equivalent. Inclusion Criteria- iC9-CAR19 Cell Infusion * Subjects must fulfill all of the following inclusion criteria to participate in this study: * As determined by the enrolling physician or protocol designee, ability of the subject to understand and comply with study procedures. Exclusion Criteria- iC9-CAR19 Cell Infusion * Subjects meeting any of the following criteria cannot be enrolled in this study: * Corticosteroid use is contraindicated following iC9-CAR19 infusion unless medically necessary (e.g., to treat CRS). * Severe systemic uncontrolled disease or toxicities that develop after lymphodepletion may prompt exclusion from cell infusion at the discretion of the investigator. * Received any donor lymphocyte infusions (DLI) ≤6 weeks prior to iC9-CAR19 T cell product administration. * Received any T cell lytic or toxic antibody (e.g. alemtuzumab) ≤8 weeks prior to iC9- CAR19 T cell product administration (residual lytic levels may destroy the infused iC9- CAR19 T cells and/or prevent their in vivo expansion). Inclusion Criteria Prior to Lymphodepletion for the Second Infusion * Life expectancy ≥ 12 weeks. * Documentation of absence of human anti-mouse antibodies (HAMA). Demonstrate adequate renal and hepatic function as defined below; all screening labs to be obtained within 72 hours prior to lymphodepletion. Subject meets at least one of the following criteria: * B-cell recovery (defined as absolute CD19+ cell count of \>50/μL in the blood or bone marrow CD19+ B cells ≥0.5% of marrow aspirate cells by flow cytometry) within 6 months of initial infusion. Subjects who meet this criteria within 6 months of initial infusion may be started on lymphodepletion at a date later than 6 months from initial infusion. * MRD positive (defined as ≥0.01% as assessed by multi-parameter flow cytometry) with CD19+ expression at any time after initial infusion. * At least 4 weeks have passed since the initial iC9-CAR19 T cell infusion. * Subjects have resolved/recovered symptoms from CRS and/or ICANS that developed after prior iC9-CAR19 T cell infusion. * Subjects must have autologous transduced activated T cells that meet the Certificate of Analysis (CofA) acceptance criteria. The subject must have sufficient available cells or have sufficient stored peripheral blood to manufacture additional iC9-CAR19 T cells. Exclusion Criteria for Lymphodepletion for the Second Infusion Subjects meeting any of the following criteria cannot receive a second infusion as part of this study: * Pregnant or breastfeeding (Note: breast milk cannot be stored for future use if the milk is collected while the mother is being treated on study). * Has a known additional malignancy that is active and/or progressive requiring treatment; exceptions include basal cell or squamous cell skin cancer, in situ cervical or bladder cancer, or other cancer for which the subject has been disease-free for at least five years. * Subjects must not have tumor in a location where enlargement could cause airway obstruction. * Subjects may not have an oxygen requirement as defined by pulse oximetry of \<90% on room air. * Patients who are on treatment an active uncontrolled infections with resolution of signs/symptoms are not excluded. Non-influenza, non-RSV, isolated upper respiratory infections are not excluded. Other active uncontrolled infections will be excluded. * Use of systemic corticosteroids at doses ≥10 mg/day prednisone or its equivalent; those receiving \<10 mg/day may be enrolled at discretion of investigator. (Note: Corticosteroid use with doses at the discretion of the treating physician are allowed after procurement up to the beginning of lymphodepletion.). Physiologic replacement with hydrocortisone is allowed at 6-12 mg/m2/day, or equivalent. Inclusion Criteria- Second iC9-CAR19 Cell Infusion Subjects must fulfill all of the following inclusion criteria to receive a second iC9- CAR19 cell infusion on this study: Exclusion Criteria- Second iC9-CAR19 Cell Infusion Subjects meeting any of the following criteria cannot receive a second iC9-CAR19 cell infusion on this study: * Corticosteroid use is contraindicated following iC9-CAR19 infusion unless medically necessary (e.g., to treat CRS). * Severe systemic uncontrolled disease or toxicities that develop after lymphodepletion may prompt exclusion from cell infusion at the discretion of the investigator

Study Info

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