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Clinical Trials/NCT01809600
NCT01809600
Completed
Not Applicable

Rituximab-Containing Immunochemotherapy for Burkitt's Lymphoma (BL) and High-Grade B-Cell Lymphoma, Unclassifiable, With Features Intermediate Between Diffuse Large B-Cell Lymphoma and BL

Gachon University Gil Medical Center1 site in 1 country43 target enrollmentFebruary 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Burkitt's Lymphoma
Sponsor
Gachon University Gil Medical Center
Enrollment
43
Locations
1
Primary Endpoint
Event-free survival
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

This retrospective study is aimed at evaluating the safety and efficacy of rituximab-containing immunochemotherapy in adult patients with Burkitt's lymphoma (BL) or high-grade B-cell lymphoma, unclassifiable, with features intermediate between diffuse large B-cell lymphoma and BL.

Detailed Description

Inclusion criteria 1. pathologically confirmed BL or BL-U by World Health Organization 2008 criteria 2. age \>20 yrs 3. received rituximab+chemotherapy as first-line treatment 4. with measurable or evaluable lesion 5. with complete set of clinical and laboratory data for the analysis

Registry
clinicaltrials.gov
Start Date
February 2013
End Date
March 2014
Last Updated
9 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Junshik Hong

Assistant Professor, Department of Internal Medicine

Gachon University Gil Medical Center

Eligibility Criteria

Inclusion Criteria

  • pathologically confirmed Burkitt's lymphoma (BL) or High grade B-cell lymphoma, unclassifiable, with features intermediate between diffuse large B-cell lymphoma and BL (BL-U) by WHO 2008 criteria
  • age \>20 yrs
  • received rituximab+chemotherapy as first-line treatment
  • with measurable or evaluable lesion

Exclusion Criteria

  • patients with BL or BL-U previously treated with rituximab

Outcomes

Primary Outcomes

Event-free survival

Time Frame: one year

Event-free survival is measured from the time from treatment initiation to any treatment failure including disease progression, or discontinuation of treatment for any reason (eg, disease progression, toxicity, patient preference, initiation of new treatment without documented progression, or death)

Secondary Outcomes

  • complete response rate(1-year)
  • overall survival(1-year)
  • Grade 4 hematologic toxicities(one year)

Study Sites (1)

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