Treatment of Macroglobulinemic Lymphoma With 2CdA, Cyclophosphamide and Rituximab

This study is ongoing, but not recruiting participants.
Sponsor:
Information provided by (Responsible Party):
M.D. Anderson Cancer Center
ClinicalTrials.gov Identifier:
NCT00667329
First received: April 24, 2008
Last updated: April 18, 2013
Last verified: April 2013

April 24, 2008
April 18, 2013
July 1999
July 2014   (final data collection date for primary outcome measure)
Study goal is to see how well the drugs 2CdA, cyclophosphamide, and rituximab (rituxan) shrink a lymphoma called Waldenstrom's macroglobulinemia. [ Time Frame: 10 Years ] [ Designated as safety issue: No ]
The goal of this clinical research study is to see how well the drugs 2CdA, cyclophosphamide, and rituximab (rituxan) shrink a lymphoma called Waldenstrom's macroglobulinemia. [ Time Frame: 10 Years ] [ Designated as safety issue: No ]
Complete list of historical versions of study NCT00667329 on ClinicalTrials.gov Archive Site
  • After these drugs are given for 2 courses, a second goal is to see how long a remission lasts. [ Time Frame: 10 Years ] [ Designated as safety issue: No ]
  • A third goal is to see how often repeat remissions can be achieved when the lymphoma returns later and the same drugs are restarted. [ Time Frame: 10 Years ] [ Designated as safety issue: No ]
Same as current
Not Provided
Not Provided
 
Treatment of Macroglobulinemic Lymphoma With 2CdA, Cyclophosphamide and Rituximab
Primary Treatment of Macroglobulinemic Lymphoma With 2CdA, Cyclophosphamide and Rituximab

Primary Objectives:

  1. To assess frequency and complete response in newly diagnosed patients with Waldenstrom's macroglobulinemia treated with 2CdA, cyclophosphamide and rituximab.
  2. To assess duration of unmaintained remission and frequency of recontrol with resumption of treatment.

Before the study starts, patients will have a complete exam. Blood and urine tests will be done. A bone marrow test, a chest x-ray and a CT scan of the abdomen will be done if not studied recently.

Blood tests will be repeated after 14, 21, and 42 days. Provided the disease has responded, another bone marrow sample will be taken to confirm remission. X-rays may be repeated for the same reason.

The patient or a family member will be taught to inject 2CdA under the skin three times a day for 7 days. The patient will also take cyclophosphamide by mouth twice each day. Rituxan will be given by vein once weekly for 4 weeks after a test infusion on the day prior to the first injection. A second course of the 3 drugs will be given about 6 weeks after the start of the first course. All patients with improving disease will then be followed without further treatment.

This is an investigational study. The FDA has approved each of these drugs for the treatment of low-grade lymphoma. The combined use of these drugs for Waldenstrom's macroglobulinemia is investigational, although each drug has been effective by itself for this disease. About 50 patients will take part in this study. This study will take place only at UTMDACC (outpatient basis).

Interventional
Not Provided
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Lymphoma
  • Drug: 2CdA
    1.5 mg/m^2 subcutaneous injection three times daily x 7 days.
    Other Names:
    • Leustatin
    • Cladribine
  • Drug: Cyclophosphamide
    40 mg/m^2 PO twice daily x 7 days.
    Other Names:
    • Cytoxan
    • Neosar
  • Drug: Rituximab
    375 mg/m^2 IV once weekly x 4 weeks.
    Other Name: Rituxan
Experimental: 2CdA + Cyclophosphamide + Rituximab
2CdA 1.5 mg/m^2 subcutaneous injection three times daily x 7 days. Cyclophosphamide 40 mg/m^2 PO twice daily x 7 days. Rituximab 375 mg/m^2 IV once weekly x 4 weeks.
Interventions:
  • Drug: 2CdA
  • Drug: Cyclophosphamide
  • Drug: Rituximab
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Active, not recruiting
50
Not Provided
July 2014   (final data collection date for primary outcome measure)

Inclusion Criteria:

  1. Newly diagnosed patients with symptomatic macroglobulinemic lymphoma are eligible. Macroglobulinemic lymphoma includes patients with either biopsy proven small lymphocytic lymphoma or chronic lymphocytic leukemia and monoclonal IgM. Also included are symptomatic patients with clonal proliferation producing a pathologic monoclonal IgM that causes cryoglobulinemia, peripheral neuropathy or cold agglutinin hemolytic anemia.
  2. Patients must have adequate liver function (bilirubin <2.5 mg%) and renal function (creatinine <2.0 mg%).

Exclusion Criteria:

None.

Both
Not Provided
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00667329
DM99-070
No
M.D. Anderson Cancer Center
M.D. Anderson Cancer Center
Not Provided
Principal Investigator: Donna M. Weber, MD M.D. Anderson Cancer Center
M.D. Anderson Cancer Center
April 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP