Rituximab and Combination Chemotherapy in Treating Patients With Newly Diagnosed, HIV-Associated Burkitt's Lymphoma

NCT00392834 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 34

Last updated 2018-06-06

Study results available
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Summary

RATIONALE: Monoclonal antibodies, such as rituximab, can block cancer growth in different ways. Some block the ability of cancer cells to grow and spread. Others find cancer cells and help kill them or carry cancer-killing substances to them. Drugs used in chemotherapy work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Giving rituximab together with combination chemotherapy may kill more cancer cells.

PURPOSE: This phase II trial is studying how well giving rituximab together with combination chemotherapy works in treating patients with newly diagnosed, HIV-associated Burkitt's lymphoma.

Conditions

Interventions

BIOLOGICAL

filgrastim

given subcutaneously

BIOLOGICAL

pegfilgrastim

given subcutaneously

BIOLOGICAL

rituximab

given IV

DRUG

cyclophosphamide

given IV

DRUG

cytarabine

given intrathecally

DRUG

doxorubicin hydrochloride

given IV

DRUG

etoposide

given IV

DRUG

ifosfamide

given IV

DRUG

leucovorin calcium

given IV

DRUG

liposomal cytarabine

given intrathecally

DRUG

methotrexate

given intrathecally

DRUG

therapeutic hydrocortisone

given intrathecally

DRUG

vincristine sulfate

given IV

Sponsors & Collaborators

  • National Cancer Institute (NCI)

    collaborator NIH
  • The Emmes Company, LLC

    collaborator INDUSTRY
  • AIDS Malignancy Consortium

    lead NETWORK

Principal Investigators

  • Ariela Noy, MD · Memorial Sloan Kettering Cancer Center

  • David M. Aboulafia, MD · Floyd & Delores Jones Cancer Institute at Virginia Mason Medical Center

  • Lawrence D. Kaplan, MD · University of California, San Francisco

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
120 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-09-30
Primary Completion
2011-07-31
Completion
2013-07-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00392834 on ClinicalTrials.gov