Non Hodgkin Lymphoma Clinical Trial

Phase II Trial of CHOP-R Followed by Zevalin and Rituxan in Follicular Lymphoma

Summary

The purpose of this study is to determine the complete response rate when CHOP-R chemotherapy in followed by Zevalin in previous untreated patients with follicular lymphoma

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Full Description

Patients with follicular lymphoma who require therapy and have been previously untreated are eligible for this non-randomized, phase II study evaluating up front therapy with CHOP-R x 3 cycles followed by zevalin and 4 additional weeks of rituxan.The complete response will be determined by combining IWC criteria and PET scanning.Secondary objectives include PET-CT conversion rate, frequency and severity of adverse events, duration of complete remission and time to next lymphoma therapy.

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Eligibility Criteria

Inclusion Criteria:

Conformed diagnosis of follicular lymphoma, grades 1,2 or 3
No prior chemotherapy
No prior monoclonal antibody therapy
Bulky or symptomatic disease, stage II-IV
Performance status 0-2

Exclusion Criteria:

Impaired bone marrow reserve
Presence of CNS lymphoma
Serious nonmalignant disease or active infection

Study is for people with:

Non Hodgkin Lymphoma

Phase:

Phase 2

Estimated Enrollment:

60

Study ID:

NCT00177554

Recruitment Status:

Completed

Sponsor:

University of Pittsburgh

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There is 1 Location for this study

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UPMC Cancer Centers
Pittsburgh Pennsylvania, 15232, United States

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Study is for people with:

Non Hodgkin Lymphoma

Phase:

Phase 2

Estimated Enrollment:

60

Study ID:

NCT00177554

Recruitment Status:

Completed

Sponsor:


University of Pittsburgh

How clear is this clinincal trial information?

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