Study of Natural Killer Cells in Bone Marrow and Blood Samples From Patients With and Without Hematologic Cancer

Sponsor
Case Comprehensive Cancer Center (Other)
Overall Status
Terminated
CT.gov ID
NCT00918658
Collaborator
National Cancer Institute (NCI) (NIH)
34
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35
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Study Details

Study Description

Brief Summary

RATIONALE: Collecting and storing samples of bone marrow and blood from patients with cancer to study in the laboratory may help doctors find better ways to treat the cancer.

PURPOSE: This research study is looking at natural killer cells in bone marrow and blood samples from patients with hematologic cancer and from patients who do not have cancer.

Condition or Disease Intervention/Treatment Phase
  • Other: biologic sample preservation procedure
  • Other: immunologic technique
  • Other: laboratory biomarker analysis

Detailed Description

OBJECTIVES:
  • To collect normal and malignant cells in bone marrow and peripheral blood samples from patients with acute myeloid leukemia, acute lymphoblastic leukemia, chronic myelogenous leukemia, or multiple myeloma and from patients with no malignancy to use as target cells in cytotoxicity assays.

  • To collect information about HLA type and immunophenotype of malignant cells as determined by clinical flow cytometry.

OUTLINE: Bone marrow aspirates and/or peripheral blood samples are collected and used as target cells in standard cytotoxicity assays, with notch-induced natural killer (N-NK) cells as the effector cells, to determine whether N-NK cells are capable of killing malignant cells and/or non-malignant cells. Receptor-blocking antibodies may be added to determine which NK cell receptors are responsible for malignant cell recognition and killing.

Information about HLA type and immunophenotype of the malignant cells is collected from the patient's medical record.

Study Design

Study Type:
Observational
Actual Enrollment :
34 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
Collection of Bone Marrow and Peripheral Blood for Testing of Notch-induced Natural Killer Cell Activity
Study Start Date :
Apr 1, 2008
Actual Primary Completion Date :
Mar 1, 2011
Actual Study Completion Date :
Mar 1, 2011

Arms and Interventions

Arm Intervention/Treatment
Patients with hematologic cancer

Patients with acute myeloid leukemia, acute lymphoblastic leukemia, chronic myelogenous leukemia, or multiple myeloma

Other: biologic sample preservation procedure
All specimens will be collected using the Pathology Residual Tissue Procurement.

Other: immunologic technique
Information about HLA type and immunophenotype of the malignant cells is collected from the patient's medical record.

Other: laboratory biomarker analysis
Bone marrow aspirates and/or peripheral blood samples are collected and used as target cells in standard cytotoxicity assays, with notch-induced natural killer (N-NK) cells as the effector cells, to determine whether N-NK cells are capable of killing malignant cells and/or non-malignant cells. Receptor-blocking antibodies may be added to determine which NK cell receptors are responsible for malignant cell recognition and killing.

Patients without cancer

Patients who do not have cancer.

Other: biologic sample preservation procedure
All specimens will be collected using the Pathology Residual Tissue Procurement.

Other: immunologic technique
Information about HLA type and immunophenotype of the malignant cells is collected from the patient's medical record.

Other: laboratory biomarker analysis
Bone marrow aspirates and/or peripheral blood samples are collected and used as target cells in standard cytotoxicity assays, with notch-induced natural killer (N-NK) cells as the effector cells, to determine whether N-NK cells are capable of killing malignant cells and/or non-malignant cells. Receptor-blocking antibodies may be added to determine which NK cell receptors are responsible for malignant cell recognition and killing.

Outcome Measures

Primary Outcome Measures

  1. Collection of normal and malignant cells to use as target cells in cytotoxicity assays [We anticipate collecting approximately 30 samples in total, over a 1-2 year period.]

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
DISEASE CHARACTERISTICS:
  • Meets one of the following criteria:

  • No evidence of malignancy

  • Diagnosis of one of the following:

  • Acute myeloid leukemia

  • Acute lymphoblastic leukemia

  • Chronic myelogenous leukemia

  • Multiple myeloma

PATIENT CHARACTERISTICS:
  • Not specified
PRIOR CONCURRENT THERAPY:
  • Not specified

Contacts and Locations

Locations

Site City State Country Postal Code
1 Case Medical Center, University Hospitals Seidman Cancer Center, Case Comprehensive Cancer Center Cleveland Ohio United States 44106-5065

Sponsors and Collaborators

  • Case Comprehensive Cancer Center
  • National Cancer Institute (NCI)

Investigators

  • Principal Investigator: Rose Beck, MD, PhD, Case Medical Center, University Hospitals Seidman Cancer Center, Case Comprehensive Cancer Center

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Case Comprehensive Cancer Center
ClinicalTrials.gov Identifier:
NCT00918658
Other Study ID Numbers:
  • CASE2Z08
  • P30CA043703
  • CASE2Z08
  • CASE-2Z08-CC502
First Posted:
Jun 11, 2009
Last Update Posted:
Oct 9, 2015
Last Verified:
Oct 1, 2015

Study Results

No Results Posted as of Oct 9, 2015