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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00582725
Other study ID # HO02401
Secondary ID NCI-2011-00578
Status Completed
Phase Phase 2
First received
Last updated
Start date March 2002
Est. completion date November 2010

Study information

Verified date May 2014
Source University of Wisconsin, Madison
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Patients will receive 6 to 8 cycles of R-CHOP (Rituximab, Cyclophosphamide, doxorubicin, vincristine, and prednisone), with GM-CSF.


Description:

The objective of this study is to estimate complete response rates for patients treated with this regimen, to assess overall response rates, event-free survival and overall survival; and to assess toxicities associated with R-CHOP + GM-CSF. Patients will receive 6 to 8 cycles of R-CHOP (Rituximab, Cyclophosphamide, doxorubicin, vincristine, and prednisone), with GM-CSF.


Recruitment information / eligibility

Status Completed
Enrollment 38
Est. completion date November 2010
Est. primary completion date December 2005
Accepts healthy volunteers No
Gender All
Age group 60 Years and older
Eligibility Inclusion Criteria:

- Histologically confirmed, CD20+ B cell diffuse large cell lymphoma, with measurable or evaluable disease

- Having no prior chemotherapy, immunotherapy or radiotherapy except for one cycle of CHOP or R-CHOP.

Exclusion Criteria:

- Pregnant

- Hepatitis B Surface Antigen positive

- Have known CNS disease or HIV infection

- Have NY Classification III or IV disease.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
R-CHOP+GM-CSF
addition of GM-CSF

Locations

Country Name City State
United States University Of Wisconsin Madison Wisconsin

Sponsors (1)

Lead Sponsor Collaborator
University of Wisconsin, Madison

Country where clinical trial is conducted

United States, 

References & Publications (1)

Kahl BS, Bailey HH, Smith EP, Turman N, Smith J, Werndli J, Williams EC, Longo WL, Kim KM, McGovern J, Jumonville A. Phase II study of weekly low-dose paclitaxel for relapsed and refractory non-Hodgkin's lymphoma: a Wisconsin Oncology Network Study. Cance — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Response Rate to Therapy Dec 2005 approx
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