Post-transplant Autologous Cytokine-induced Killer (CIK) Cells for Treatment of High Risk Hematologic Malignancies
Primary Purpose
Leukemia, Multiple Myeloma
Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
CIK cells
etoposide
bcnu
cyclophosphamide
gemcitabine
vinorelbine
melphalan
Sponsored by
About this trial
This is an interventional prevention trial for Leukemia
Eligibility Criteria
Inclusion Criteria:
Patients between 18 and 75 years of age, inclusive candidates for standard autologous SCT who are at high risk for relapse:
- Acute myelogenous leukemia (AML), high risk, in CR1 or beyond without a donor (CR1 defined as: normal bone marrow morphology, resolution of any previously abnormal karyotype, neutrophils > 1000/ul, platelets > 100,000/ul, independence from red cell transfusion, no evidence extramedullary leukemia)
- Hodgkin's lymphoma relapsed or refractory, with the presence of >= 1 adverse risk factor (Adverse risk factors are defined as stage IV involvement of the lung or bone marrow, constitutional symptoms, and the presence of more than minimal residual disease before the preparatory regimen)
- Multiple myeloma with high risk features with only single autologous transplant option. High risk features defined as IgA myeloma, B2M > 2.5 mg/ml with normal kidney function, complex karyotypes or isolated chromosome 13 abnormalities, standard-dose therapy > 12 months, or inability to achieve at least 50% reduction of plasma cells in the bone marrow or 50% reduction in the paraprotein concentration after initial induction chemotherapy prior to transplant.
- Patients must have ECOG performance status < 2
- Patients must have adequate renal function with a serum creatinine of < 2 mg/dl or creatinine clearance > 50 ml/min.
- Patients must have adequate liver function with a total bilirubin < 2 mg/dl or transaminases < 3 times the upper limit of normal.
- Patients must have negative antibody serology for human immunodeficiency virus (HIV1 and 2)
- Adult women and minorities will be included. Patients with childbearing potential must use effective contraception.
- Patients must sign informed consent prior to initiation of any study-related treatments.
Exclusion Criteria:
- ECOG performance status > 2
- LVEF < 45%
- Pulmonary diffusion capacity < 50% predicted
- Total bilirubin > 2 mg/dl
- Creatinine > 2 mg/dl
- Pregnancy
- Patients positive for HIV
- Patients with engraftment failure at day 42 post transplant defined as failure to achieve a granulocyte count > 500/ul on 3 successive daily determinations and an unsupported platelet count of >= 50,000/ul by day 42
- Patients with active, uncontrolled infection that is expected to continue beyond day 42-63.
- Patients who fail to collect sufficient quantities of stem cells (> 1.6 x 10^9 cells) during apheresis to support CIK cell expansion cultures.
Sites / Locations
- Stanford University School of Medicine
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Autologous Cytokine-induced Killer Cells
Arm Description
Outcomes
Primary Outcome Measures
To document the toxicities of infusion of autologous CIK cells
Measure freedom from progression (FFP)
Measure event free survival
Measure overall survival
Secondary Outcome Measures
Measure disease response
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT00477035
Brief Title
Post-transplant Autologous Cytokine-induced Killer (CIK) Cells for Treatment of High Risk Hematologic Malignancies
Official Title
A Phase I Study of Post-transplant Autologous Cytokine-induced Killer (CIK) Cells for the Treatment of High-risk Hematologic Malignancies
Study Type
Interventional
2. Study Status
Record Verification Date
January 2017
Overall Recruitment Status
Completed
Study Start Date
May 2006 (undefined)
Primary Completion Date
March 2011 (Actual)
Study Completion Date
March 2011 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Sally Arai
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of the study is to conduct a phase I study of adoptive immunotherapy with autologous, ex-vivo expanded cytokine-induced killer (CIK) cells to reduce the relapse rate in autologous stem cell transplant patients with high-risk hematologic malignancies.
Detailed Description
Disease relapse remains the major cause of treatment failure in autologous stem cell transplantation for patients with high-risk disease. Relapse after autologous transplant is in part due to the persistence of residual cancer cells. Cellular immunotherapy using activated autologous effector cells to recognize and kill tumor targets in a minimal disease state after transplant is a strategy being explored to reduce relapse and improve survival. We hypothesize that cytokine-induced killer (CIK) cell-based immunotherapy can reduce the relapse rate after high-risk autologous stem cell transplantation by treating post-transplant minimal residual disease.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Leukemia, Multiple Myeloma
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
22 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Autologous Cytokine-induced Killer Cells
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
CIK cells
Other Intervention Name(s)
autologous cytokine-induced killer cells
Intervention Description
2x10e8 cells/kg
Intervention Type
Drug
Intervention Name(s)
etoposide
Other Intervention Name(s)
Eposin, Etopophos, Vepesid, VP-16
Intervention Description
60 mg/kg
Intervention Type
Drug
Intervention Name(s)
bcnu
Other Intervention Name(s)
Carmustine
Intervention Description
15 mg/kg
Intervention Type
Drug
Intervention Name(s)
cyclophosphamide
Other Intervention Name(s)
Endoxan, Cytoxan, Neosar, Procytox, Revimmune, cytophosphane
Intervention Description
100 mg/kg
Intervention Type
Drug
Intervention Name(s)
gemcitabine
Other Intervention Name(s)
Gemzar
Intervention Description
1250 mg/m2
Intervention Type
Drug
Intervention Name(s)
vinorelbine
Other Intervention Name(s)
Navelbine
Intervention Description
30 mg/m2
Intervention Type
Drug
Intervention Name(s)
melphalan
Other Intervention Name(s)
Alkeran, Melphalan hydrochloride
Intervention Description
200 mg/m2
Primary Outcome Measure Information:
Title
To document the toxicities of infusion of autologous CIK cells
Time Frame
Day 42 post autologous stem cell transplant
Title
Measure freedom from progression (FFP)
Time Frame
1 and 2 years post-transplant
Title
Measure event free survival
Time Frame
1 and 2 years post-transplant
Title
Measure overall survival
Time Frame
1 and 2 years post-transplant
Secondary Outcome Measure Information:
Title
Measure disease response
Time Frame
at day 40-60, day 90, day 180, and yearly
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients between 18 and 75 years of age, inclusive candidates for standard autologous SCT who are at high risk for relapse:
Acute myelogenous leukemia (AML), high risk, in CR1 or beyond without a donor (CR1 defined as: normal bone marrow morphology, resolution of any previously abnormal karyotype, neutrophils > 1000/ul, platelets > 100,000/ul, independence from red cell transfusion, no evidence extramedullary leukemia)
Hodgkin's lymphoma relapsed or refractory, with the presence of >= 1 adverse risk factor (Adverse risk factors are defined as stage IV involvement of the lung or bone marrow, constitutional symptoms, and the presence of more than minimal residual disease before the preparatory regimen)
Multiple myeloma with high risk features with only single autologous transplant option. High risk features defined as IgA myeloma, B2M > 2.5 mg/ml with normal kidney function, complex karyotypes or isolated chromosome 13 abnormalities, standard-dose therapy > 12 months, or inability to achieve at least 50% reduction of plasma cells in the bone marrow or 50% reduction in the paraprotein concentration after initial induction chemotherapy prior to transplant.
Patients must have ECOG performance status < 2
Patients must have adequate renal function with a serum creatinine of < 2 mg/dl or creatinine clearance > 50 ml/min.
Patients must have adequate liver function with a total bilirubin < 2 mg/dl or transaminases < 3 times the upper limit of normal.
Patients must have negative antibody serology for human immunodeficiency virus (HIV1 and 2)
Adult women and minorities will be included. Patients with childbearing potential must use effective contraception.
Patients must sign informed consent prior to initiation of any study-related treatments.
Exclusion Criteria:
ECOG performance status > 2
LVEF < 45%
Pulmonary diffusion capacity < 50% predicted
Total bilirubin > 2 mg/dl
Creatinine > 2 mg/dl
Pregnancy
Patients positive for HIV
Patients with engraftment failure at day 42 post transplant defined as failure to achieve a granulocyte count > 500/ul on 3 successive daily determinations and an unsupported platelet count of >= 50,000/ul by day 42
Patients with active, uncontrolled infection that is expected to continue beyond day 42-63.
Patients who fail to collect sufficient quantities of stem cells (> 1.6 x 10^9 cells) during apheresis to support CIK cell expansion cultures.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sally Arai
Organizational Affiliation
Stanford University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Stanford University School of Medicine
City
Stanford
State/Province
California
ZIP/Postal Code
94305
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Post-transplant Autologous Cytokine-induced Killer (CIK) Cells for Treatment of High Risk Hematologic Malignancies
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