Non Hodgkin Lymphoma Clinical Trial

PK-directed Dose Adjustment of IV Busulfan Conditioning Regimen for Autologous Stem Cell Transplant in Lymphoma Patients

Summary

This is a study for the outcome and safety of individualized busulfan dosing with cyclophosphamide and etoposide for patients preparing for a stem cell transplant to treat Non-Hodgkin or Hodgkin's Lymphoma.

View Full Description

Full Description

Evaluation of progression-free survival, transplant related mortality, overall survival, and overall response rate, in subjects with NHL and HL receiving an IV busulfan-based conditioning regimen with PK-guided IV busulfan dosing, followed by autologous HSCT as well as comparison to those receiving carmustine, etoposide, cytarabine, and melphalan (BEAM) conditioning regimen (and its variants) obtained from registry data in the Center for International Blood and Marrow Transplant Research (CIBMTR) Assessment of the safety profile of a BuCyE conditioning regimen with PK-directed dosing of IV busulfan will also be completed.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Subjects with NHL to be included:

Any subject with NHL that had relapsed or progressed following initial therapy with an anthracycline-based chemotherapy regimen and has achieved a subsequent partial remission (PR) or a complete remission (CR) following a salvage chemotherapy regimen.
Any subject with NHL that was initially refractory to an anthracycline-based chemotherapy regimen but who has achieved a PR or CR following a salvage chemotherapy regimen.
Any subject with an initial International Prognostic Index (IPI) score 4-5 who achieved a PR or any CR following an anthracycline-based chemotherapy regimen except subjects with Mantle cell, T cell and Natural Killer (NK) cell pathologies.
Subjects with Mantle cell, T cell and NK cell lymphoma may be enrolled if they have PR or CR after initial therapy.
Any subject that has relapsed or progressed following previous autologous HSCT.

Subjects with HL to be included:

Any subject with HL that had relapsed or progressed following initial therapy with an multi-drug chemotherapy regimen and has achieved a subsequent PR or a CR following a salvage chemotherapy regimen.
Any subject with HL that is initially refractory to a multi-drug chemotherapy regimen but who has achieved a PR or CR following a salvage chemotherapy regimen.
Any subject that has relapsed or progressed following previous autologous HSCT.

Exclusion Criteria:

Any subject with chemoresistant disease by demonstration of less than PR to most recent chemotherapy, and any subject with prior treatment history of autologous HSCT or high-dose chemotherapy with stem cell rescue for any medical reason will be excluded.

Excluded will also be subjects with existing or active central nervous system lymphoma or human immunodeficiency virus related lymphoma, unacceptable organ function, or uncontrolled infections.

Study is for people with:

Non Hodgkin Lymphoma

Phase:

Phase 2

Estimated Enrollment:

207

Study ID:

NCT00948090

Recruitment Status:

Completed

Sponsor:

Otsuka Pharmaceutical Development & Commercialization, Inc.

Check Your Eligibility

Let’s see if you might be eligible for this study.

What is your age and gender ?

Submit

There are 41 Locations for this study

See Locations Near You

University of Alabama in Birmingham
Birmingham Alabama, 35294, United States
Arizona Cancer Center
Tucson Arizona, 85719, United States
Alta Bates Summit Medical Center
Berkeley California, 94704, United States
Scripps Clinic
La Jolla California, 92037, United States
UCSD Medical Center BMT Program
La Jolla California, 92093, United States
Cedars-Sinai Medical Center
Los Angeles California, 90048, United States
Sutter Cancer Center
Sacramento California, 95816, United States
University of California, Davis Medical Center
Sacramento California, 95817, United States
University of California San Francisco Medical Center
San Francisco California, 94143, United States
Rocky Mountain Cancer Centers
Denver Colorado, 80218, United States
Florida Hospital Cancer Institute
Orlando Florida, 32804, United States
Emory University
Atlanta Georgia, 30322, United States
University of Illinois Cancer Center
Chicago Illinois, 60612, United States
The University of Chicago
Chicago Illinois, 60637, United States
Loyola University Chicago
Maywood Illinois, 60153, United States
Bone Marrow and Stem Cell Transplant Program
Indianapolis Indiana, 46202, United States
University of Kansas Medical Center
Westwood Kansas, 66205, United States
LSU Health Sciences Center at Shreveport/Feist Weiller Cancer Center
Shreveport Louisiana, 71103, United States
University of Maryland Medical Center - Marlene & Stewart Greenebaum Cancer Center
Baltimore Maryland, 21201, United States
University of Michigan
Ann Arbor Michigan, 48109, United States
University of Nebraska Medical Center
Omaha Nebraska, 68198, United States
Montefiore-Einstein Cancer Center
Bronx New York, 10467, United States
Weill Cornell Medical College
New York New York, 10065, United States
University of North Carolina at Chapel Hill
Chapel Hill North Carolina, 27514, United States
Duke University Medical Center
Durham North Carolina, 27710, United States
University of Oklahoma Health Sciences Center
Oklahoma City Oklahoma, 73104, United States
Oregon Health & Science University
Portland Oregon, 97239, United States
The Western Pennsylvania Hospital
Pittsburgh Pennsylvania, 15224, United States
Medical University of South Carolina
Charleston South Carolina, 29425, United States
Sarah Cannon Research Institute
Nashville Tennessee, 37203, United States
Baylor University Medical Center
Dallas Texas, 75246, United States
South Texas Veterans Health Care System
San Antonio Texas, 78229, United States
Texas Transplant Physician Group, PLLC
San Antonio Texas, 78229, United States
Huntsman Cancer Institute
Salt Lake City Utah, 84112, United States
Virginia Commonwealth University
Richmond Virginia, 23298, United States
Fred Hutchinson Cancer Research Center
Seattle Washington, 98109, United States
West Virginia University Hospital
Morgantown West Virginia, 26506, United States
Saint John Regional Hospital
Saint John New Brunswick, E2L 4, Canada
Queen Elizabeth II Health Sciences Centre - VG Site
Halifax Nova Scotia, B3H 2, Canada
The Ottawa Hospital
Ottawa Ontario, K1H 8, Canada
Royal Victoria Hospital MUHC
Montreal Quebec, H3A 1, Canada
Saskatoon Cancer Centre
Saskatoon Saskatchewan, S7N 4, Canada

How clear is this clinincal trial information?

Study is for people with:

Non Hodgkin Lymphoma

Phase:

Phase 2

Estimated Enrollment:

207

Study ID:

NCT00948090

Recruitment Status:

Completed

Sponsor:


Otsuka Pharmaceutical Development & Commercialization, Inc.

How clear is this clinincal trial information?

×

Introducing, the Journey Bar

Use this bar to access information about the steps in your cancer journey.

Please confirm you are a US based health care provider:

Yes, I am a health care Provider No, I am not a health care provider