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Cell Samples From Patients With Leukemia

Xenotransplantation of Primary Leukemia Samples Into Zebrafish

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01395628
Enrollment
10
Registered
2011-07-15
Start date
2011-07-31
Completion date
Unknown
Last updated
2016-05-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Leukemia

Keywords

chronic phase chronic myelogenous leukemia, childhood acute promyelocytic leukemia (M3), childhood acute myeloid leukemia/other myeloid malignancies, adult acute myeloid leukemia with t(8;21)(q22;q22), adult acute myeloid leukemia with del(5q), adult acute promyelocytic leukemia (M3)

Brief summary

RATIONALE: Studying samples of blood and tissue from patients with cancer in the laboratory may help doctors learn more about cancer and the development of drug resistance in patients. It may also help doctors find better ways to treat cancer. PURPOSE: This research trial is studying samples from patients with leukemia.

Detailed description

OBJECTIVES: * Demonstrate the capability of primary human leukemia samples to survive and proliferate in the zebrafish embryo. * Confirm the anti-proliferative or toxic effects of known chemotherapeutics on the transplanted cells in vivo. * Evaluate the effect of novel anticancer drugs and/or their combinations on individual samples. OUTLINE: This is a multicenter study. Cryopreserved specimens are injected into the yolk sac of zebrafish embryos under anesthesia. After 1 hour of recovery at 28° C, embryos are maintained at 38° C and screened for fluorescence at the injection site. Within 48 hours post-injection, some embryos are treated with various chemotherapeutic drugs or dimethyl sulfoxide and incubated in protease solution. Proliferation of leukemia cells are monitored by live-cell microscopy. Cells with or without drug treatment are then extracted at 24 and 72 hours post-injection. Leukemia cells are counted and tested with imatinib mesylate, all-trans retinoic acid (tretinoin), cytosine arabinose, and known bioactive chemical compounds from promising drug families, such as tyrosine kinase inhibitors, antiapoptotic agents, channel modulators, and prostaglandin agonists.

Interventions

OTHERcell proliferation assay
OTHERlaboratory biomarker analysis

Sponsors

National Cancer Institute (NCI)
CollaboratorNIH
Children's Oncology Group
Lead SponsorNETWORK

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
No minimum to 30 Years
Healthy volunteers
No

Inclusion criteria

DISEASE CHARACTERISTICS: * Samples of blood and tissue cells from patients diagnosed with myeloid disease including the following subtypes: * Chronic phase chronic myeloid leukemia (CML), to complement initial studies in the K562 CML cell line * Acute promyelocytic leukemia (APL), to complement initial studies in the NB4 APL cell line * Acute myeloid leukemia (AML) expressing the t(8;21)(q22;q22) translocation, which occurs in approximately 12% of pediatric AML and is associated with good prognosis * AML expressing 5q- or monosomy 7, associated with a poor prognosis * AML expressing the fms-like tyrosine kinase 3 internal tandem duplication (FLT3-ITD), associated with a poor prognosis PATIENT CHARACTERISTICS: * Not specified PRIOR CONCURRENT THERAPY: * Not specified

Design outcomes

Primary

MeasureTime frame
Primary human leukemia samples capable to survive and proliferate in the zebrafish embryo
In vivo confirmation of anti-proliferative or toxic effects of known chemotherapeutic agents on the transplanted cells
Effects of novel anticancer drugs and/or their combinations on individual samples

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026