Clinical Trials /

Randomized Study of Haploidentical Hct and Subsequent Donor nk Cell Infusion in High-risk AML and MDS

NCT02477787

Description:

This is a single center, open label, random comparison phase 2b study. The primary objective of this study is, by random comparison, to assess the anti-leukemia effect of allogeneic, donor-derived natural killer (NK) cells infused after HLA-haploidentical hematopoietic cell transplantation (HCT) in patients with refractory acute myelogenous leukemia (AML). The secondary objectives of the study are to assess the side effects of donor NK cell infusion, effects of donor NK cell infusion upon HCT outcomes, as well as effects upon post-HCT immune recovery.

Related Conditions:
  • Acute Myeloid Leukemia
  • Myelodysplastic Syndromes
Recruiting Status:

Recruiting

Phase:

Phase 2

Trial Eligibility

Document

Title

  • Brief Title: Randomized Study of Haploidentical Hct and Subsequent Donor nk Cell Infusion in High-risk AML and MDS
  • Official Title: Randomized Comparative Study for Efficacy and Safety Evaluation of HLA-haploidentical Hematopoietic Cell Transplantation With or Without Post-transplant Allogeneic Donor-derived Natural Killer Cell Infusion in High-risk Acute Myelogenous Leukemia and Myelodysplastic Syndrome

Clinical Trial IDs

  • ORG STUDY ID: 2014-1091
  • NCT ID: NCT02477787

Conditions

  • Acute Myelogenous Leukemia

Interventions

DrugSynonymsArms
allogeneic, donor-derived NK cellstreatment

Purpose

This is a single center, open label, random comparison phase 2b study. The primary objective of this study is, by random comparison, to assess the anti-leukemia effect of allogeneic, donor-derived natural killer (NK) cells infused after HLA-haploidentical hematopoietic cell transplantation (HCT) in patients with refractory acute myelogenous leukemia (AML). The secondary objectives of the study are to assess the side effects of donor NK cell infusion, effects of donor NK cell infusion upon HCT outcomes, as well as effects upon post-HCT immune recovery.

Detailed Description

      5.0 Study design

      5.1. Study patient should be enrolled by PI Kyoo-Hyung Lee, MD or Young-Shin Lee, RN.

      5.2. Random assignment 5.2.1. Patients were randomly assigned to study arms the day before
      initiation of conditioning therapy (day -8).

      5.2.2. Stratification Refractory AML Stratification 1: Primary refractory vs.
      relapse-refractory/2 or more relapse Stratification 2: peripheral blood blast <5% vs. ≥5%
      5.2.3. extra leukapheresis will be performed form donors assigned to treatment cohort.

      High-risk AML Stratification: AML in CR1 with high-risk features vs. AML CR2

      High-risk myelodysplastic syndrome (MDS) IPSS intermediate-2 risk vs. IPSS high-risk

      6.0. Patient Eligibility

      6.1. Patients with refractory AML Refractory AML is defined as follows;

        1. Primary refractory: failure to achieve complete remission (CR) after 2 cycles of
           induction chemotherapy; or, in patient ≥65 years of age, progressive AML after treatment
           with hypomethylating agent (increase in peripheral blood blast by 50% or increase in
           bone marrow blast by 25%)

        2. Relapse then refractory: recurrence of AML, which is refractory to standard salvage
           chemo therapy; or, in patient ≥65 years of age, to hypomethylating agent

        3. AML in ≥2 relapses

      6.2. Patients in AML CR1 with high-risk chromosomal features such as complex abnormality (3
      or more abnormalities), -5, 5q-, -7, 7q-, 11q32 abn (non t(9;11)), inv(3), t(3;3), t(6;9),
      t(9;22), or monosomal karyotype of 2 abnormalites or Patients in AML CR2

      6.3 Patients with MDS, in intermediate-2 or high risk categories by IPSS classification

      6.4. Patients should be 19 years of age or older

      6.5. Patients should have Karnofsky performance scale ≥70

      6.6. Patients and cell donors must understand fully and sign informed consent forms

      Exclusion

      6.7. Pregnant or lactating women

      6.8. Patient with abnormal liver function (total bilirubin ≥ 5.0 mg/dl, AST ≥ 5 times upper
      normal limits)

      6.9. Patients with abnormal renal function (creatinine ≥ 3.0 mg/dl)

      6.10. Patients with clinically-evident cardiac or pulmonary dysfunction

      6.11. Patients with infection that is progressive despite appropriate anti-microbial
      treatment

      6.12 Patients with hypersensitivity to gentamicin

      6.13. Patients who had received allogeneic cell therapy

      7.0.Treatment Plan

      7.1. For the study group of patients, donor NK cells will be generated from the hematopoietic
      cells. Donor NK cell will be produced in the GCP laboratory at Asan Institute of Life Science
      by a team of Stem Cell Research Center, Korea Research Institute of Bioscience and
      Biotechnology.

      7.2. Patients will have a triple-lumen Hickman central-venous catheter (CVC) placed. Chest
      X-ray should be taken after CVC placement to confirm the location and the absence of hematoma
      formation or pneumothorax.

      7.3. Lumbar puncture will be done and preservative free methotrexate 10 mg/m2 (not to exceed
      15 mg total) will be given intrathecally.

      7.4. Menstruating women will be given norethindrone (Norlutate) 10 mg po daily.

      7.5. The preparative regimen (Bu-Flu-ATG; also see Appendix V): 7.5.1. Busulfex (Bu) 3.2
      mg/kg/day iv daily on days -7 and -6. Patients who are older than 64 years of age or who have
      significant co-morbidities may receive Bu on day -7 only.

      7.5.2. Fludarabine (Flu) 30 mg/m2/day in D5W 100 ml iv over 30 minutes starting at 4 pm daily
      on days -7, -6, -5, -4, -3, and -2.

      7.5.3. Methylprednisolone 2 mg/kg in D5W 100 ml iv over 30 minutes on days -4, -3, -2, and
      -1.

      7.5.4. Anti-thymocyte globulin (Thymoglobulin, Genzyme Transplant, Cambridge, MA, USA) 2.5
      mg/kg/day in N/S 500-800 ml (less than 4 mg/ml) iv over 4 hours starting at 8 am daily on
      days -3, -2, and -1.

      7.6. Hematopoietic stem cell collection from the donors. 7.6.1. The HLA-haploidentical family
      donor will receive granulocyte colony-stimulating factor (G-CSF, Grasin) 10 ug/kg by
      subcutaneous (sc) injection for 5 days (from day -3 to day 1). Daily CBC will be done. On
      days 0, 1, and 2, peripheral blood mononuclear cells will be collected by leukapheresis
      (Amicus, Fenwal). A female donor or one with poor peripheral vein may have a Quinton or
      Groshong catheter placed. A sample will be taken for cell count of total cells, mononuclear
      cells, CD34+ cells, CD3+ cells, CD4+ cells, and CD8+ cells. Cells collected on days 0 and 1,
      will be transplanted to the patients on the same day without further manipulation. At least
      2x106/kg of CD34+ cells should be collected on day 0. If not, additional collection may be
      scheduled under the discretion of attending physician. G-CSF is the most commonly
      administered agent to donors for cell-collection and there has been no documented long-term
      side effect document during last 25 years' use. However, the cell donors in the study will be
      monitored for possible side effect of G-CSF.

      7.6.2. Cell collected on collected on day 2 will be transported to the GCP laboratory for the
      generation of NK cells (study arm). For details of donor NK cell generation, please see
      appendix V.

      7.7. Peripheral blood hematopoietic cell infusion for transplantation (days 0 or 0-1 or 0-2).

      7.7.1. For ABO matched or minor mismatched transplantation, premedication with Avil 45.5 mg
      iv push and acetaminophen 600 mg po will be given. Stem cells will be infused via CVC over 1
      hour.

      7.7.2 For major ABO mismatched transplantation, premedication with Avil 45.5 mg iv push,
      acetaminophen 600 mg po, 10% mannitol 100 g iv over 4 hours beginning 30 minutes before stem
      cell infusion, and hydrocortisone 250 mg iv immediately before and 30 minutes of stem cell
      infusion will be given. Stem cells will be infused via CVC over 1 hour.

      Donor NK cell infusion (see appendix V) 7.8. The patients in the study arm will receive donor
      NK cell infusion around days 13 and 20. A permissible range of infusion time will be +/- 3
      days.

      7.9. For DNKI to be given on day 13 (DNKI-1), the cell dose is 1-2 x108/kg or about the half
      of amount generated. For DNKI to be given on day 20 (DNKI-2), the cell dose is up to
      5x108/kg. 7.10. Avil 1 ampoule will be given intravenously 30 minutes prior to each NK cell
      infusions.

      8.0 Supportive cares. 8.1. Dilantin 15 mg/kg (ABW) in NS 200 ml iv over 1 hour for loading on
      day -8, then 200 mg po bid through day -6 or -5.

      8.2. Clotrimazole powder to groin, axilla, and perianal area bid from day -8 until absolute
      neutrophil count (ANC) > 3,000/ul.

      8.3. Sodium bicarbonate/saline mouthwash qid until mucositis is resolved. 8.4.. Micafungin 50
      mg iv qd from Day 1 to ANC > 3,000/ul. 8.5. Ciprofloxacin 500 mg po bid (for selective bowel
      decontamination) until ANC > 3,000/ul. With the first fever spike, ciprofloxacin is
      discontinued and broad spectrum antibiotics are begun.

      8.6. Acyclovir 250 mg/m2 iv twice a day will be given from day 1, and will be changed into
      acyclovir 400 mg po bid until the discontinuation of cyclosporine administration.

      8.7. G-CSF 450ug iv daily from day 5 to ANC >3,000/ul. 8.8. The patients are hydrated with
      0.9 % NS at 100 ml/hr while the patients are receiving busulfan.

      8.9. Azithromycin 125 mg iv or po daily starting when ANC >500/ul until 1 year if there is no
      evidence of GVHD. In patients with GVHD, azithromycin will be continued until resolution of
      GVHD and discontinuation of immunosuppressive therapy.

      8.10. Bactrim 2 t po once a day three times a week when ANC >3,000/ul. 8.11. Intravenous
      immunoglobulin 500 mg/kg (ABW) iv over 6 hours every 2 weeks starting day 7 until day 90 then
      monthly until day 180.

      9. GVHD prophylaxis 9.1. Cyclosporine 1.5 mg/kg in N/S 100 ml iv over 2-4 hours q12 hrs
      beginning day -1. Adjust cyclosporine dose to provide appropriate blood level (100-300 ng/ml
      in whole blood) and according to the change of renal function.

      9.2. Cyclosporine dosing will be changed to oral dosing when oral feeding became feasible.
      Provided that there is no GVHD, cyclosporine dose will be tapered by 10%-20% every 2-4 weeks
      starting between days 30 and 60 of HCT.

      9.3. Cytomegalovirus (CMV) and Epstein-Barr virus (EBV) monitoring: Blood CMV antigenemia
      assay and quantitative EBV PCR will be done at least weekly starting day -7 until day 100. If
      CMV antigenemia is positive, preemptive treatment with ganciclovir will be considered as
      follows; 5 mg/kg iv (every 12 hours for 7 days then) once daily until 1-2 weeks after the
      negative conversion of CMV antigenemia. When EBV DNA is detected by PCR, infusion of
      rituximab 375 mg/m2 will be considered weekly until the DNA is no longer detectable.

      9.4. CNS prophylaxis: Preservative-free methotrexate will be administered intrathecally after
      the patient recovered platelet count to over 50,000/mcl. Methotrexate 10 mg/m2 (not to exceed
      15 mg total) will be given intrathecally once every 2 weeks for three times (total four doses
      including one given before preparatory regimen).

      10.0. Treatment Evaluation

      10.1. Donor work up will include HLA-A, -B, -C, and -DRB1 typing based on PCR-sequencing
      methods, ABO/Rh typing, CBC with reticulocyte count, chemistry, BUN/phosphorus, electrolytes,
      coagulation battery, urinalysis with microscopy, EKG, chest PA and lateral, HBsAg, HBsAb, HCV
      Ab, HIV Ab, VDRL, CMV(IgG), HSV(IgG), EBV serology, Toxoplasma titer (IgG), VZV (IgG)
      (Appendix II).

      10.2. Patient work up will include; HLA-A, -B, -C, and -DRB1 typing based on PCR-sequencing
      methods, ABO/Rh typing, CBC with reticulocyte count, chemistry, BUN/phosphorus, electrolytes,
      coagulation battery, urinalysis with microscopy, MUGA scan or echocardiogram, dental consult
      and Panorex films, ENT consult and PNS films, PFT with DLCO, Chest X-ray, EKG, diagnostic
      lumbar puncture with fluid battery (cell count, glucose, protein, LD, fungal and bacterial
      cultures, cytospin), bone marrow aspirate and biopsy with cytogenetics and appropriate
      molecular tests (such as bcr-abl, pml-rara, aml1-eto), HBsAg, HBsAb, HBcAb (IgG), HCV Ab, HIV
      Ab, VDRL, CMV (IgG, IgM), HSV (IgG, IgM), EBV serology, Toxoplasma titer (IgG), VZV (IgG),
      serum pregnancy test (beta-hCG) in females, and isoagglutinin titers if ABO mismatched HCT.

      10.3. The status of mixed chimerism will be evaluated by PCR analysis of short tandem repeats
      (STRs) by multiplex primers. The chimerism status will be analyzed from whole blood DNA after
      1, 3, and 6 months after HCT.

      10.4. Blood cytomegalovirus (CMV) antigenemia and quantitative EBV PCR assays will be done at
      least weekly until day 100 of HCT.

      10.5. Immune recovery of the patients after stem cell transplantation will be monitored by
      lymphocyte subset count (Appendix VII) and measurement of Ig G, Ig M, Ig A levels and Ig G
      subset (G1, G2, G3) on 1, 3, 6, and 12 months after HCT.

      10.6. The patients will be followed with physical examination and appropriate blood test
      including CBC at least every 3 months for 3 years after transplantation and then yearly
      thereafter.

      10.7. Bone marrow examination with cytogenetics will be done 3 to 4 weeks after HCT and,
      subsequently, as deemed necessary.

      10.8. 5 ml of bone marrow and 15 ml of heparinized blood obtained on day -8 will be sent to
      Asan-KRIBB laboratory for immune phenotyping and functional analysis. In addition, 15 ml of
      heparinized blood obtained 1, 3, 6, and 12 months after HCT will be sent to Asan-KRIBB
      laboratory for immune phenotyping and functional analysis (see Appendices VII and VIII).

      10.9.Plasma cytokine (interferon-&#947;, TNF-α, IL-6, IL-15, soluble IL-2 receptor) levels will be
      measured at 1, 3, 6, and 12 months after HCT.

      10.10. On the day of DNKI (days 13 and 20), 5 ml of heparinized peripheral blood will be sent
      to Asan-KRIBB laboratory for ATG titer determination.

      10.11. 96 assessable patients will be enrolled (48 in DNKI arm; 48 in control arm). After
      enrollment of 40 patients, interim analysis will be performed.

      10.12. The enrollment period is 60 months from the approval from Korean Ministry of Food and
      Drug Safety.

      10.13. Continuous variables will be compared using T-test or Mann-Whitney test. Categorical
      variables will be compared using chi-square test. Lastly, time-event variables will be
      compared using log-rank test with optional multivariate analysis if necessary.

      10.14. Patients will be removed from the study immediately, if the patient withdraws the
      consent to participate in the study.

      11.0. Definition of Endpoints and Response

      11.1.The occurrence and severity of side effects of NK cell infusion observed in the study
      will be monitored and graded according to the Common Toxicity Criteria v3.0(2006; National
      Cancer Institute). GVHD will be diagnosed and graded by published criteria listed in Appendix
      III. TRM will be defined as any death occurring after the transplantation without leukemia
      progression.

      11.2.CR is defined as blast less than 5% in the marrow with recovery of neutrophil count over
      1,000/ul and no extramedullary disease. CRmarrow is defined as blast less than 5% in the
      marrow, no blast in the peripheral blood, neutrophil count over 500/ul, platelet count over
      20,000/ul, and no extramedullary disease.

      11.3.Leukemia recurrence is defined as over 5% leukemia blasts in a bone marrow sample after
      a previously documented CR. In patients with persistent leukemia after HCT, the day of
      leukemia progression was defined as the day on which leukemia blasts reappeared in peripheral
      blood with bone marrow examination showing over 5% persistent blasts.

      11.4. Event-free survival will be measured from the day of HCT to leukemia recurrence,
      transplantation-related mortality, or the last follow-up. Overall survival will be measured
      from the HCT to death from any cause or the last follow-up.
    

Trial Arms

NameTypeDescriptionInterventions
treatmentExperimentalpatients will receive donor-derived NK cell infusion after haploidentical HCT
    controlNo Interventionpatients will undergo haploidentical HCT but not receive donor-derived NK cells after HCT

      Eligibility Criteria

              Inclusion Criteria:
      
                -  Patients with refractory AML Refractory AML is defined as follows;
      
                     1. Primary refractory: failure to achieve complete remission (CR) after 2 cycles of
                        induction chemotherapy; or, in patient ≥65 years of age, progressive AML after
                        treatment with hypomethylating agent (increase in peripheral blood blast by 50%
                        or increase in bone marrow blast by 25%)
      
                     2. Relapse then refractory: recurrence of AML, which is refractory to standard
                        salvage chemo therapy; or, in patient ≥65 years of age, to hypomethylating agent
      
                     3. AML in ≥2 relapses
      
                -  Patients should be 19 years of age or older
      
                -  Patients should have Karnofsky performance scale ≥70
      
                -  Patients and cell donors must understand fully and sign informed consent forms
      
              Exclusion Criteria:
      
                -  Pregnant or lactating women
      
                -  Patient with abnormal liver function (total bilirubin ≥ 5.0 mg/dl, AST ≥ 5 times upper
                   normal limits)
      
                -  Patients with abnormal renal function (creatinine ≥ 3.0 mg/dl)
      
                -  Patients with clinically-evident cardiac or pulmonary dysfunction
      
                -  Patients with infection that is progressive despite appropriate anti-microbial
                   treatment
      
                -  Patients with hypersensitivity to gentamicin
      
                -  Patients who had received allogeneic cell therapy previously.
            
      Maximum Eligible Age:80 Years
      Minimum Eligible Age:19 Years
      Eligible Gender:All
      Healthy Volunteers:Accepts Healthy Volunteers

      Primary Outcome Measures

      Measure:number of patients who experience progression/recurrence of AML after HCT
      Time Frame:up to 60 months
      Safety Issue:
      Description:

      Secondary Outcome Measures

      Measure:number of patients who achieve engraftment after HCT
      Time Frame:up to 6 months
      Safety Issue:
      Description:
      Measure:number of patients who develop acute GVHD
      Time Frame:up to 4 months
      Safety Issue:
      Description:
      Measure:number of patients who develop chronic GVHD
      Time Frame:up to 60 months
      Safety Issue:
      Description:
      Measure:number of patients who experience donor NK cell infusion-associated toxicity
      Time Frame:up to 1 month
      Safety Issue:
      Description:
      Measure:number of patients who die after HCT without progression of AML
      Time Frame:up to 60 months
      Safety Issue:
      Description:

      Details

      Phase:Phase 2
      Primary Purpose:Interventional
      Overall Status:Recruiting
      Lead Sponsor:Asan Medical Center

      Trial Keywords

      • HLA-haploidentical hematopoietic cell transplantation
      • natural killer cells

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