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CD34 Selection of the Peripheral Blood Stem Cell Graft for Autologous Transplant
This study is ongoing, but not recruiting participants.
First Received: September 14, 2005   Last Updated: July 10, 2007   History of Changes
Sponsored by: Stanford University
Information provided by: Stanford University
ClinicalTrials.gov Identifier: NCT00186680
  Purpose

Evaluate the feasibility and safety of autologous transplantation of CD34+Thy-1+ hematopoietic stem cells afer high dose marrow ablative chemotherapy in patients with breast cancer.


Condition Intervention Phase
Breast Cancer
Procedure: high dose chemo then auto hematopoietic cell transplant
Phase I
Phase II

Genetics Home Reference related topics: breast cancer
MedlinePlus related topics: Breast Cancer Cancer
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment
Official Title: Selection of CD34+THY-1 Positive Cells From Peripheral Blood Cells Procured for Autologous Hematopoietic Support Following High Dose Treatment With BCNU, Cyclophosphamide & Cisplatin for Stage IV Breast Cancer & Limited Prior Treatment

Further study details as provided by Stanford University:

Primary Outcome Measures:
  • Feasibility and safety

Secondary Outcome Measures:
  • efficiency of mobilization
  • tumor contamination

Study Start Date: September 1996
  Eligibility

Ages Eligible for Study:   19 Years to 70 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • stage IV breast cancer
  • primary breast cancer does not express CD34+
  • adequate organ function
  • no evidence of active infection

Exclusion Criteria:

  • chemotherapy within 4 weeks
  • CNS disease
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00186680

Locations
United States, California
Stanford University Cancer Center
Stanford, California, United States, 94305
Sponsors and Collaborators
Stanford University
Investigators
Principal Investigator: Ginna Laport, MD Stanford University
  More Information

No publications provided

Study ID Numbers: BMT86
Study First Received: September 14, 2005
Last Updated: July 10, 2007
ClinicalTrials.gov Identifier: NCT00186680     History of Changes
Health Authority: United States: Institutional Review Board

Keywords provided by Stanford University:
Stage IV Breast Cancer

Study placed in the following topic categories:
Cisplatin
Skin Diseases
Breast Neoplasms
Cyclophosphamide
Breast Diseases

Additional relevant MeSH terms:
Neoplasms
Neoplasms by Site
Skin Diseases
Breast Neoplasms
Breast Diseases

ClinicalTrials.gov processed this record on May 07, 2009