NCT00923442

Brief Summary

This study will collect tumor samples from people with cancers of the blood, bone marrow, or lymph glands for laboratory study of the biology of these conditions. Such studies contribute to a better understanding of cancer biology and to the development of new treatments. Planned studies include:

  • Examination of individual cancer cells and to search for differences compared to other types of cancer and normal cells
  • Examination of the chromosomes and genes in cancer cells and to search for differences compared to other types of cancer and normal cells
  • Development of sensitive methods to detect small amounts of cancer that remain after treatment
  • Search for new cancer proteins that might serve as targets for treatment
  • Investigation of methods to develop cancer vaccines. Patients from \>= 1 to 75 years of age with acute lymphocytic leukemia, acute myelogenous leukemia, myelodysplastic syndrome, chronic myelogenous leukemia, juvenile myelomonocytic leukemia, non-Hodgkin's lymphoma, Hodgkin's disease, and other hematologic malignancies may be eligible for this study. Blood or bone marrow samples will be collected when sampling is required for the patient's medical care. Cells from some individuals will be grown in test tubes, establishing cell lines or in animals, establishing xenograft models. (A xenograft is transplantation of cells of one species to another species.)

Trial Health

73
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
550

participants targeted

Target at P75+ for all trials

Geographic Reach
1 country

1 active site

Status
enrolling by invitation

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 24, 2004

Completed
5.3 years until next milestone

First Submitted

Initial submission to the registry

June 17, 2009

Completed
1 day until next milestone

First Posted

Study publicly available on registry

June 18, 2009

Completed
Last Updated

April 27, 2026

Status Verified

April 17, 2026

First QC Date

June 17, 2009

Last Update Submit

April 24, 2026

Conditions

Keywords

Acute Lymphoblastic LeukemiaAcute Lymphocytic LeukemiaPediatric Blood DisordersHodgkins and non-Hodgkins lymphomaMDSNatural History

Outcome Measures

Primary Outcomes (1)

  • Tissue acquisition for lab investigations

    The examination of biologic assays relevant to the investigation of hematologic malignancies

    1 Month

Study Arms (1)

1

patients (from \>/= 1 to 75 years old) diagnosed with any hematologic malignancy or pre-malignant condition

Eligibility Criteria

Age1 Year - 120 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Tumor tissue of patients whose ages range from birth to 75 years old diagnosed with any hematologic malignancy or pre-malignant blood disorder

You may qualify if:

  • Confirmed pathological diagnosis of any hematologic malignancy or pre-malignant blood disorder, including but not restricted to the following:
  • Acute Lymphocytic Leukemia (ALL)
  • Acute Myelogenous Leukemia (AML)
  • Myelodysplastic Syndrome (MDS)
  • Chronic Myelogenous Leukemia (CML)
  • Juvenile Myelomonocytic Leukemia (JMML, J-CML)
  • Non-Hodgkin's Lymphoma (NHL)
  • Hodgkin's Disease
  • Tumor tissue that has been previously collected and is available for study or that can be collected with minimal additional risk to the subject during sampling required for routine patient care.
  • Age: \>= 1 years.
  • Prior therapy: no restrictions
  • Subject, parent/guardian, legally authorized representative (LAR), or durable power of attorney must be able to give informed consent and sign the informed consent document.

You may not qualify if:

  • None

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

National Institutes of Health Clinical Center

Bethesda, Maryland, 20892, United States

Location

Related Links

MeSH Terms

Conditions

Precursor Cell Lymphoblastic Leukemia-LymphomaMyelodysplastic SyndromesLymphoma, Non-HodgkinLeukemia, Myeloid, AcuteHodgkin Disease

Condition Hierarchy (Ancestors)

Leukemia, LymphoidLeukemiaNeoplasms by Histologic TypeNeoplasmsHematologic DiseasesHemic and Lymphatic DiseasesLymphoproliferative DisordersLymphatic DiseasesImmunoproliferative DisordersImmune System DiseasesBone Marrow DiseasesLymphomaLeukemia, Myeloid

Study Officials

  • John W Glod, M.D.

    National Cancer Institute (NCI)

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
NIH
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 17, 2009

First Posted

June 18, 2009

Study Start

February 24, 2004

Last Updated

April 27, 2026

Record last verified: 2026-04-17

Data Sharing

IPD Sharing
Will share

All IPD recorded in the medical record will be shared with intramural investigators upon request.

Shared Documents
STUDY PROTOCOL, SAP, ICF
Time Frame
Clinical data available during the study and indefinitely.
Access Criteria
Clinical data will be made available via subscription to BTRIS and with the permission of the study PI.

Locations