Pathogenesis of Hematologic Malignancies

Sponsor
OHSU Knight Cancer Institute (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT01728402
Collaborator
National Institutes of Health (NIH) (NIH), National Cancer Institute (NCI) (NIH)
5,000
1

Study Details

Study Description

Brief Summary

The cause of blood and bone marrow cancers is poorly understood; however, most research focuses on how cancer cells grow and develop. Because the causes of these cancers are unknown, current treatments may be unnecessarily harsh and often do not provide a cure. Identifying the causes of blood cancers would allow for the development of treatments that are more likely to provide a cure. To find the causes of blood and bone marrow cancers, we will look for specific cancer cell abnormalities that are responsible for cancer cell growth. We will then look to see if drugs that can reverse these abnormalities can kill cancer cells.

Condition or Disease Intervention/Treatment Phase
  • Procedure: blood draw, bone marrow procedure, or tissue biopsy

Study Design

Study Type:
Observational
Anticipated Enrollment :
5000 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Pathogenesis of Acute Leukemia, Lymphoproliferative Disorders, and Myeloproliferative Disorders
Study Start Date :
Sep 1, 2008

Arms and Interventions

Arm Intervention/Treatment
Blood Draw

Procedure: blood draw, bone marrow procedure, or tissue biopsy

Outcome Measures

Primary Outcome Measures

  1. Identify and determine the frequency of mutations causing aberrant signaling pathway function in patients with acute leukemias (AL), lymphoproliferative disorders (LPD), myelodysplastic syndromes (MDS), and myeloproliferative neoplasms (MPN) [After laboratory analyses are complete. Lab samples are collected at the time of a scheduled blood draw, bone marrow procedure, tissue biopsy, or other visit for usual medical care]

    Integrated functional genomics studies (whole genome sequencing, RNAi, proteomics, drug sensitivity, expression profiling) will be used to identify aberrant signaling pathways that contribute to the formation of hematologic malignancies.

Eligibility Criteria

Criteria

Ages Eligible for Study:
1 Year and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Suspected or confirmed diagnosis of AL, LPD, MDS, or MPD

  • Male or female of all ages

  • Willing and able to sign informed consent

  • Willing guardian consent for participants under 18 years of age

Exclusion Criteria:
  • No suspected or confirmed diagnosis of acute leukemias (AL), lymphoproliferative disorders (LPD), myelodysplastic syndromes (MDS), or myeloproliferative diseases (MPD)

Contacts and Locations

Locations

Site City State Country Postal Code
1 OHSU Knight Cancer Institute Portland Oregon United States 97239

Sponsors and Collaborators

  • OHSU Knight Cancer Institute
  • National Institutes of Health (NIH)
  • National Cancer Institute (NCI)

Investigators

  • Principal Investigator: Marc Loriaux, MD, OHSU Knight Cancer Institute

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Marc Loriaux, Associate Professor, OHSU Knight Cancer Institute
ClinicalTrials.gov Identifier:
NCT01728402
Other Study ID Numbers:
  • IRB00004422
  • 5R21CA159265
First Posted:
Nov 19, 2012
Last Update Posted:
Feb 18, 2022
Last Verified:
Feb 1, 2022

Study Results

No Results Posted as of Feb 18, 2022