Clinical trial

A Phase II Trial Of BEAM/Rituximab/Autologous Hematopoietic Stem Cell Transplantation (AHSCT) For Patients With CD20 Positive Non-Hodgkin's Lymphoma

Name
0063-02-FB
Description
RATIONALE: Monoclonal antibodies, such as rituximab, can locate cancer cells and either kill them or deliver cancer-killing substances to them without harming normal cells. Drugs used in chemotherapy, such as carmustine, cytarabine, etoposide, and melphalan, work in different ways to stop cancer cells from dividing so they stop growing or die. Combining rituximab and combination chemotherapy with autologous stem cell transplantation may allow the doctor to give higher doses of chemotherapy drugs and kill more cancer cells. PURPOSE: Phase II trial to study the effectiveness of combining rituximab with combination chemotherapy followed by autologous hematopoietic stem cell transplantation in treating patients who have B-cell non-Hodgkin's lymphoma.
Trial arms
Trial start
2002-05-08
Estimated PCD
2005-11-01
Trial end
2015-03-12
Status
Completed
Phase
Early phase I
Treatment
rituximab
Arms:
Arm 1
Other names:
Rituxan
carmustine
Arms:
Arm 1
Other names:
Gliadel Wafer, Bicnu
cytarabine
Arms:
Arm 1
Other names:
cytosine arabinoside
etoposide
Arms:
Arm 1
Other names:
Etopophos, Toposar
melphalan
Arms:
Arm 1
Other names:
Evomela
autologous bone marrow transplantation
Arms:
Arm 1
peripheral blood stem cell transplantation
Arms:
Arm 1
Size
68
Primary endpoint
evaluation of the relationship between levels of sCD20 in the blood of patients with non-Hodgkin's lymphoma pre and post rituximab/BEAM/autologous peripheral blood progenitor cell transplantation (PBPCT) as they relate to clinical outcomes.
pre and post transplant
Eligibility criteria
Inclusion Criteria: * Diagnosis of non-Hodgkin's lymphoma o Any B cell * CD20-positive disease * Failed prior primary induction therapy * Meets 1 of the following criteria: * Chemotherapy-refractory disease * Received at least 3 prior chemotherapy regimens * Mantle cell lymphoma * Eligible for transplantation * 19 years old and over * WHO 0-2 * Life expectancy at least 6 months * Absolute neutrophil count ≥ 1,000/mm\^3\* * Platelet count \> 50,000/mm\^3\* * Hemoglobin \> 9.0 g/dL\* o NOTE: \*Unless due to lymphomatous involvement of the bone marrow * Fertile patients must use 2 methods of effective contraception Exclusion Criteria: * No history of T-cell lymphoma * Not pregnant or nursing * No other concurrent serious disease or condition that would preclude study participation
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE2'], 'designInfo': {'allocation': 'NA', 'interventionModel': 'SINGLE_GROUP', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'NONE'}}, 'enrollmentInfo': {'count': 68, 'type': 'ACTUAL'}}
Updated at
2023-10-06

1 organization

1 product

4 drugs

1 indication

Indication
lymphoma
Product
melphalan