CIK-Cells in Relapsing Patients With Acute Leukemia or Myelodysplastic Syndromes After SCT.

NCT ID: NCT02752243

Last Updated: 2022-04-01

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 32 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2016-03-31
• Study Completion Date: 2024-03-31

Brief Summary

Multi-site, non-randomized Phase I/II study involving children and adults.

Detailed Description

This is a phase I/II multicenter-study to investigate the feasibility safety and efficacy of interleukin (IL)-15 activated CIK cells in patients with acute leukemia or myelodysplastic syndrome (MDS) showing evidence of relapse after allogeneic stem cell transplantation (SCT).

CIK cell infusions will be given with an interval of 4-6 weeks according to a dose escalation schedule in patients with impending relapse after allogeneic SCT. In presence of acute graft versus host disease (aGvHD) ≥ grade II, the next scheduled infusion will not be administered.

Conditions

Myelodysplastic Syndromes; Acute Leukemia

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

CIK-Cells

IL-15 activated CIK cells individually generated from PB mononuclear cells of the original stem cell donors.

Group Type: EXPERIMENTAL

CIK-Cells

Intervention Type: DRUG

IL-15 activated CIK cells individually generated from PB mononuclear cells of the original stem cell donors.

Interventions

CIK-Cells

IL-15 activated CIK cells individually generated from PB mononuclear cells of the original stem cell donors.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

Acute leukemia and MDS patients with molecular or cytogenetic relapse in peripheral blood (PB) or bone marrow (BM) samples obtained during monitoring for relapse after allogeneic SCT.

MRD detected by Ig/TCR gene rearrangement testing or any detected disease specific DNA or RNA sequence or disease specific cell surface Proteins or mixed recipient chimerism (MC) ≥ 1% and < 40%, or levels ≥ 10-4 of BCR-ABL/ABL ratio or any other disease specific cytogenetic abnormality will trigger CIK cell interventions.

• Respecting MC, MC = 1% of autologous/recipient signals in PB samples must be confirmed by another PB or BM sample within one week. Patients with MC = 1% of autologous/recipient signals in CD33+ and/or CD34+ subpopulations in PB samples must be confirmed by BM analyses within one week. Acute leukemia and MDS patients with MC = 1% of autologous/recipient signals including signals in CD33+ and/or CD34+ subpopulations in BM samples must not be confirmed.
• Acute leukemia and MDS patients with frank relapse ≥ 120 days after allogeneic SCT who achieved complete remission (CR) or blast clearance (i.e. <5% blasts) in the bone marrow after re-induction chemotherapy.
• All patients must be in complete remission or have achieved blast clearance (i.e. <5% blasts) in the bone marrow before 1st CIK cell treatment (bone marrow assessment at a maximum of 7 days in advance of 1st treatment is obligatory).
• Patients without immunosuppressive agents and steroids for at least 7 days.
• Patients without chemo- or immune therapy during CIK cell treatment, except patients with thyrosine-kinase inhibitors (TKI) for treatment of BCR-ABL positive leukemia. Last DLI treatment must be 4 weeks before 1st CIK cell treatment.
• Patients with < grade II aGvHD.
• Patients with Karnowsky or Lansky performance status ≥ 50%.
• Patients and/or his/her legal representative having reviewed the patient information/informed consent form and have had their questions answered and have given written informed consent.

Exclusion Criteria

• Acute leukemia and MDS patients with hematologic relapse < day 120 after allogeneic stem cell transplantation.
• Patients with 5% and more malignant cells in a representative bone marrow analysis performed at a maximum of 7 days before 1st CIK cell treatment (obligatory).
• Patients with immunosuppressive agents or steroids.
• Patients with chemo- or immune therapy, except patients with thyrosine-kinase inhibitors (TKI) for BCR-ABL positive leukemias.
• Patients with ≥ grade II GvHD.
• Patients with rapid T cell regeneration and any signs of GvHD
• Patients with Karnowsky or Lansky performance status < 50%.
• Patients and/or his/her legal representative having reviewed the patient information/informed consent form and have had their questions answered and have not given written informed consent.
• HIV-positive patients.
• HBV/HCV positive patients.
• Patients with prior solid organ transplantation.
• Patients treated with any other investigational product within the last 28 days or five half-lives (whichever is longer).
• Hypersensitivity to any component of the study drug
• Female patients of child-bearing potential not agreeing to use a highly effective method of birth control resulting in a low failure rate (i.e. < 1%) when used consistently and correctly.
• Male patients with female partners of childbearing potential not agreeing to use a highly effective method birth control resulting in a low failure rate (i.e. < 1%) when used consistently and correctly.
• Pregnancy/Breastfeeding.
• Patients with severe infections or signs/symptoms of infection within 2 weeks prior to study start.

• Minimum Eligible Age: 0 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Peter Bader

OTHER

Sponsor Role: lead

Responsible Party

Peter Bader

Prof. Dr. med.

Responsibility Role: SPONSOR_INVESTIGATOR

Locations

University Hospital Heidelberg, Ruprecht Karls University, Hospital for children and adolescents, Pediatrics III, Department of Oncology, Haematology, Immunology and Pneumology

Heidelberg, Baden-Wurttemberg, Germany

Division for Stem Cell Transplantation and Immunology, Department for Children and Adolescents, University Hospital Frankfurt

Frankfurt am Main, Hesse, Germany

Internal Medicine II, Department of Hematology, Oncology, Rheumatology and Infectious Diseases, Goethe-University Frankfurt/Main

Frankfurt am Main, Hesse, Germany

University Medicine Duesseldorf, Department of Paediatric Oncology, Haematology and Immunology, Bone Marrow Transplantation Unit

Düsseldorf, North Rhine-Westphalia, Germany

Internal Medicine III, Department of Hematology and Oncology, Johannes Gutenberg University

Mainz, Rhineland-Palatinate, Germany

Countries

Germany

Other Identifiers

2013-005446-11

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

FFM-CIK-Cell Study 01

Identifier Type: -

Identifier Source: org_study_id