High Dose CHOP in Lymphoma
Primary Purpose
Non-Hodgkin's Lymphoma
Status
Completed
Phase
Phase 2
Locations
Israel
Study Type
Interventional
Intervention
high-dose cyclophosphamide
Sponsored by
About this trial
This is an interventional treatment trial for Non-Hodgkin's Lymphoma focused on measuring large cell lymphoma, CHOP, cyclophosphamide, high-dose
Eligibility Criteria
Inclusion Criteria: large-cell non-Hodgkin's lymphoma IPI low-intermediate, high-intermediate and high or bulky mediastinum age 18-65 Exclusion Criteria: previous treatment for lymphoma serious concurrent systemic disease
Sites / Locations
- Department of Oncology, Rambam Medical Center
Outcomes
Primary Outcome Measures
Failure-free survival
Secondary Outcome Measures
overall survival
response rate
toxicity
Full Information
NCT ID
NCT00192764
First Posted
September 13, 2005
Last Updated
September 21, 2010
Sponsor
Rambam Health Care Campus
1. Study Identification
Unique Protocol Identification Number
NCT00192764
Brief Title
High Dose CHOP in Lymphoma
Official Title
Phase II Study of Short High-dose CHOP Chemotherapy for Aggressive Non-Hodgkin's Lymphoma
Study Type
Interventional
2. Study Status
Record Verification Date
September 2010
Overall Recruitment Status
Completed
Study Start Date
December 1996 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
September 2010 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Rambam Health Care Campus
4. Oversight
5. Study Description
Brief Summary
The study hypothesis is that intensification of CHOP by dose escalation of the most active drugs in the combination will improve treatment outcome. Patients with diffuse large-cell lymphoma are treated by high cyclophosphamide containing CHOP. The planned dose is 3000 mg/m2 which is 4 times the atandard one. Only 4 cycles are given.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Non-Hodgkin's Lymphoma
Keywords
large cell lymphoma, CHOP, cyclophosphamide, high-dose
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
45 (false)
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
high-dose cyclophosphamide
Primary Outcome Measure Information:
Title
Failure-free survival
Secondary Outcome Measure Information:
Title
overall survival
Title
response rate
Title
toxicity
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
large-cell non-Hodgkin's lymphoma
IPI low-intermediate, high-intermediate and high or bulky mediastinum
age 18-65
Exclusion Criteria:
previous treatment for lymphoma
serious concurrent systemic disease
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ron Epelbaum, MD
Organizational Affiliation
nonaffiliated
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Oncology, Rambam Medical Center
City
Haifa
Country
Israel
12. IPD Sharing Statement
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High Dose CHOP in Lymphoma
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