Clinical Trials Directory

Trials / Completed

CompletedNCT00023764

Bortezomib in Treating Patients With Lymphoproliferative Disorders

Phase II Study of PS-341 in Low Grade Lymphoproliferative Disorders

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
103 (actual)
Sponsor
National Cancer Institute (NCI) · NIH
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Phase II trial to study the effectiveness of bortezomib in treating patients who have low-grade lymphoproliferative disorders. Bortezomib may stop the growth of cancer cells by blocking the enzymes necessary for cancer cell growth.

Detailed description

PRIMARY OBJECTIVES: I. Determine the frequency and duration of complete and partial response rates in patients with grade I, II, or III follicular lymphoma or mantle cell lymphoma treated with bortezomib. SECONDARY OBJECTIVES: I. Determine the response of minimal residual disease by polymerase chain reaction (PCR) detectable or clonotypic PCR minimal residual disease in bone marrow of patients treated with this regimen. II. Determine the time to progression and overall survival of patients treated with this regimen. III. Determine the toxic effects of this regimen in these patients. OUTLINE: Patients are stratified according to disease type (follicular lymphoma vs mantle cell lymphoma). Patients receive an infusion of bortezomib over 3-5 seconds once weekly for 4 weeks. Treatment repeats every 6 weeks in the absence of disease progression or unacceptable toxicity. Patients who achieve at least a partial response lasting at least 6 months may receive retreatment. Patients are followed every 3 months for 1 year and then every 4 months for 2 years.

Conditions

Interventions

TypeNameDescription
DRUGbortezomibGiven IV

Timeline

Start date
2001-06-01
Primary completion
2009-03-01
Completion
2009-03-01
First posted
2003-01-27
Last updated
2015-12-08
Results posted
2014-04-01

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00023764. Inclusion in this directory is not an endorsement.