Lymphoma, Follicular Clinical Trial
Official title:
A Phase II Study of Bortezomib in Combination With Rituximab, Fludarabine, Mitoxantrone, and Dexamethasone (VR-FND) for Relapsed or Refractory Follicular Lymphoma
The purpose of this study is to evaluate the effectiveness and safety of combining bortezomib (Velcade) with rituximab, fludarabine, mitoxantrone, and dexamethasone in treating patients with follicular cell lymphoma.
This is a phase II study using the combination of bortezomib, rituximab, fludarabine,
mitoxantrone and dexamethasone. The combination will given over a 28 day cycle. In addition
each patient will receive Pneumocystis carinii Pneumonia (PCP) prophylaxis with
Trimethoprim/sulfamethoxazole (TMP/Sulfa) or equivalent agent. On day 4 the physician has
the option of starting granulocyte colony-stimulating factor (GCSF), granulocyte macrophage
colony-stimulating factor (GMCSF), or pegylated GCSF.
All patients who receive at least one dose of the drug will be evaluated for toxicity.
Patients will be treated with the agent for at least 2 cycles to be considered eligible for
evaluation of response. The chemotherapy dosing will continue until there is evidence of
disease progression, a second recurrence of unacceptable toxicity, or a maximum of 8 courses
of therapy.
;
Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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