A Pilot Study of Standard-Dose Rituximab, Ifosfamide, Carboplatin and Etoposide (RICE) Plus Bortezomib (Velcade) in a Dose-Escalating Fashion for Patients With Relapsed or Primary Refractory Aggressive B-Cell Non-Hodgkin’s Lymphoma Who Are Candidates for Autologous Stem Cell Transplant

This study has been terminated.
( Investigator left institution. 7 patients accrued and there is insufficient data to analyze. )

First Received on August 9, 2007.  
Last Updated on April 11, 2012  
History of Changes
This Clinical Trial Sponsored By: University of California, San Francisco
Information provided by (Responsible Party): University of California, San Francisco
ClinicalTrials.gov Identifier: NCT00515138
 

Purpose for Clinical Trial

This study seeks to determine the maximum tolerated dose of bortezomib in combination with rituximab, ifosfamide, carboplatin, and etoposide for patients with relapsed or primary refractory aggressive B-Cell Non-Hodgkin’s lymphoma (diffuse large B-cell, mantle cell, follicular grade III, transformed lymphoma). Subjects will be enrolled in cohorts of 3 at each bortezomib dose level, starting at 1 mg/m(2), and escalating to 1.3, 1.5, and 1.7 mg/m(2). Bortezomib will be given on days 1 (prior to rituximab) and 4, rituximab 375 mg/m(2)/day on days 2, 3, and 4 of a 21-day cycle. They will also receive filgrastim on days 6-13 or pegfilgrastim on day 6.

Condition Study Intervention Clinical Trial Phase
Lymphoma, B-Cell Drug: Rituximab, Ifosfamide, Carboplatin, Etoposide, Bortezomib Phase 0

Study Type: Study Interventional
Study Design: Endpoint Classification: Safety Study
Study Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: A Pilot Study of Standard-Dose Rituximab, Ifosfamide, Carboplatin and Etoposide (RICE) Plus Bortezomib (Velcade) in a Dose-Escalating Fashion for Patients With Relapsed or Primary Refractory Aggressive B-Cell Non-Hodgkin’s Lymphoma Who Are Candidates for Autologous Stem Cell Transplant

Resource links provided by NLM:

MedlinePlus related topics:
Lymphoma
Drug Information available for:
Ifosfamide
Etoposide
Carboplatin
Etoposide phosphate
Rituximab
Bortezomib

U.S. FDA Resources

Further study details as provided by University of California, San Francisco:

Primary Outcome Measures For Clinical Trial:

  • -Determine the maximum tolerated dose of bortezomib in combination with rituximab, ifosfamide, carboplatin, and etoposide for patients with relapsed or primary refractory aggressive B-cell NHL [ Time Frame: 3 years ] [ Designated as safety issue: Yes ]

Enrollment: 7
Study Start Date: May 2007
Study Completion Date: November 2011
Primary Completion Date: November 2011 (Final data collection date for primary outcome measure)
Study Intervention Details:

    Drug: Rituximab, Ifosfamide, Carboplatin, Etoposide, Bortezomib

    Bortezomib starting at 1 mg/m(2), and escalating to 1.3, 1.5, 1.7. Bortezomib will be given on Days 1 (prior to rituximab) and 4, rituximab at 375 mg/m(2) on day 1, carboplatin AUC 5 and ifosfamide with mesna, each 5 mg/m(2), on day 3 and etoposide 100 mg/m(2)/day on days 2, 3, and 4 of a 21-day cycle. They will also receive filgrastim on days 6-13 or pegfilgrastim on day 6

  Eligibility

Ages Eligible for Study:   18 Years to 70 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Aggressive B-Cell Lymphoma, CD-20 positive, in first relapse or refractory to first-line chemotherapy

    • Diffuse large B-cell Lymphoma, Mantle cell lymphoma, Follicular lymphoma (Grade III), Transformed Follicular Lymphoma
    • Rituximab is allowed
    • Prior radiation is allowed
  • 18-70 years of age
  • ECOG performance status of 0-2
  • HIV seronegative
  • Measurable disease on CT scan by international working group response criteria
  • No CNS involvement
  • Subject is considered to be a candidate for autologous stem cell transplant in the opinion of the treating physician
  • Female subject is either post-menopausal or surgically sterilized or willing to use an acceptable method of birth control
  • Male subject agrees to use an acceptable method of contraception for the duration of the study

Exclusion Criteria:

  • Platelet count of <75 x 10(9)/L
  • Absolute neutrophil count of <1.0 x 10(9)/L
  • Calculated or measured creatinine clearance of <60 mL/minute within 14 days before enrollment
  • Myocardial infarction within 6 months prior to enrollment or has New York Hospital Association Class III or IV heart failure, uncontrolled angina, severe uncontrolled ventricular arrhythmias, or electrocardiographic evidence of acute ischemia or active conduction system abnormalities. Prior to study entry, any ECG abnormality at Screening has to be documented by the investigator as not medically relevant.
  • Subject has hypersensitivity to bortezomib, boron or mannitol.
  • Female subject is pregnant or breast-feeding.
  • Subject has been treated with more than one prior chemotherapy regimen.
  • Subject has received other investigational drugs with 14 days before enrollment.
  • Serious medical or psychiatric illness likely to interfere with participation in this clinical study.
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00515138

Locations
United States, California
University of California San Francisco
San Francisco, California, United States, 94143
Sponsors and Collaborators
University of California, San Francisco
Investigators
Principal Investigator: Lawrence D. Kaplan, M.D. University of California, San Francisco
Principal Investigator: Caroline Behler, M.D. University of California, San Francisco
  More Information

Additional Information:

UCSF Cancer Center&nbsp

No publications provided

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