Safety of Fludarabine, Mitoxantrone, and Dexamethasone Plus Rituximab in the Treatment of Stage IV Indolent Lymphoma

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Article
OncologyONCOLOGY Vol 14 No 3
Volume 14
Issue 3

A total of 77 patients have been entered into an ongoing, randomized protocol integrating rituximab (Rituxan) with chemotherapy for patients with newly diagnosed stage IV indolent lymphoma. Patients are receiving FND (fludarabine

A total of 77 patients have been entered into an ongoing, randomized protocol integrating rituximab (Rituxan) with chemotherapy for patients with newly diagnosed stage IV indolent lymphoma. Patients are receiving FND (fludarabine, Novantrone, and dexamethasone) concurrently with rituximab in one arm and FND followed by rituximab in the other arm. All patients have received prophylaxis for Pneumocystis infection. A subset of patients—those with follicular lymphoma but no detectable bcl-2 gene rearrangement—are considered prognostically adverse (Lopez-Guillermo et al: Blood 93:308-3087, 1999) and are being managed with an alternating triple therapy (ATT) 10-drug regimen (Ann Oncol 5(suppl 2):S73, 1994).

Preliminary safety data are as follows:

There have been no grade 4 infections or nonhematologic toxicities. The six grade 3 infections included two catheter-related bacteremias, two other bacterial infections, and two fevers of unknown origin that responded to antibacterial therapy. There have been no unusual opportunistic infections; there has been one episode of localized herpes zoster.

CONCLUSION: It appears that the combination of FND and rituximab, administered either concurrently or sequentially, is a safe regimen.

Click here for Dr. Bruce Cheson’s commentary on this abstract.

Articles in this issue

Comparative Economic Analysis of the Treatment of Relapsed Low-Grade B-Cell Non-Hodgkin’s Lymphoma (NHL) in France Using CHOP, Fludarabine, or Rituximab
FHIT Gene, Smoking, and Cervical Cancer
Final Report on the Safety and Efficacy of Retreatment With Rituximab for Patients With Non-Hodgkins Lymphoma
Prospective, Randomized, Controlled Study of Zevalin Radioimmunotherapy Compared to Rituximab Immunotherapy for B-Cell, Non-Hodgkins Lymphoma: Interim Results
IOM Medical Error Estimates Questioned, But Legislation Considered
Less Toxic Therapies for Hodgkin’s Disease May Reduce Secondary Cancers
Preserving Fertility in Young Women With Ovarian Cancer Does Not Decrease Survival
Iodine-131 Tositumomab for Patients With Transformed, Low-Grade Non-Hodgkin’s Lymphoma: Overall Clinical Trial Experience
Survival Rates Significantly Worse For African-Americans With Endometrial Cancer
Rituximab Has Significant Activity in Patients With Chronic Lymphocytic Leukemia
Responders to Rituximab Show Continued Tumor Regression Over Time and a Progression-Free Survival That Correlates With Response Classification
PhRMA Criticizes FDA’s Proposed Rule on Antibiotic Approvals
Phase II Study of Rituximab in Combination With CHOP in Patients With Previously Untreated Intermediate- or High-Grade Non-Hodgkin’s Lymphoma
New Antibiotic Effective in Treating Gram-Positive Bacteremia
Reduced-Dose Zevalin Radioimmunotherapy for Relapsed or Refractory B-Cell Non-Hodgkin’s Lymphoma Patients With Preexisting Thrombocytopenia: Report of Interim Results of a Phase II Trial
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