Clinical Trials Directory

Trials / Completed

CompletedNCT00584766

Intensive Combo Chemo With Autologous BM Rescue for Metastatic Breast Cancer

Intensive Combination Chemotherapy With Autologous Bone Marrow Rescue for Metastatic Breast Cancer After Intitial Cytoreduction With Standard Agents: A Phase II Study

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
21 (actual)
Sponsor
University of Oklahoma · Academic / Other
Sex
Female
Age
18 Years – 55 Years
Healthy volunteers
Not accepted

Summary

To determine the therapeutic efficacy of high-dose cyclophosphamide and BCNU with autologous bone marrow transplantation after initial tumor cytoreduction for patients with receptor-negative metastatic breast carcinoma and to determine the optimal timing of CyBCNU-ABMT after initial development of metastatic breast carcinoma

Conditions

Interventions

TypeNameDescription
PROCEDUREHigh-dose chemotherapyCyclophosphamide 500 mg/m2 IV day 1; Doxorubicin 30 mg/m2 IV Day 1; Methotrexate 300 mg/m2 IV Day 8;5-FU 500 mg/m2 IV day 8; leucovorin 20 mg po q 6 h x 6 doses, day 9- cycles repeated q 21 days

Timeline

Start date
1987-10-01
Primary completion
2002-05-01
Completion
2002-05-01
First posted
2008-01-02
Last updated
2015-05-29

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00584766. Inclusion in this directory is not an endorsement.

Intensive Combo Chemo With Autologous BM Rescue for Metastatic Breast Cancer (NCT00584766) · Clinical Trials Directory