A Phase I/II Study of Post-transplant Autologous Cytokine-induced Killer (CIK) Cells for the Treatment of High-risk Hematologic Malignancies

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.

Stanford is not currently accepting new patients for this trial. You may want to check clinicaltrials.gov to see if other locations are recruiting.

Investigator(s):

Intervention(s):

  • drug : busulfan
  • drug : etoposide
  • drug : bcnu
  • drug : CIK cells
  • drug : gemcitabine
  • drug : vinorelbine
  • drug : melphalan
  • drug : cyclophosphamide

Phase: Phase 1/Phase 2

Eligibility

Ages Eligible For Study:

18 Years - 75 Years

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.

External Links

Explore related trials

Contact information

Primary Contact:

Sherry Moore 6507257951

Stanford University School of Medicine 300 Pasteur Drive Stanford, CA 94305

Stanford Medicine Resources:

Footer Links: