Fludarabine, cyclophosphamide, and dexamethasone (FluCyD) combination is effective in pretreated low-grade non-Hodgkin's lymphoma.

Abstract

PURPOSE:

Fludarabine phosphate is effective as a single agent in low-grade non-Hodgkin's lymphoma (NHL). Combined with other antineoplastic agents it enhances the antitumor effect. Our aim was to define the therapeutic efficacy and toxicity of a combination of fludarabine, cyclophosphamide and dexamethasone (FluCyD) in patients with advanced low-grade lymphoma.

PATIENTS AND METHODS:

Twenty-five adults with pretreated advanced-stage low-grade NHL were treated with three-day courses of fludarabine 25 mg/m2/day, cyclophosphamide 350 mg/m2/day, and dexamethasone 20 mg/day, every four weeks for a maximum of six courses.

RESULTS:

Of the 25 patients, 18 (72%) responded, 8 (32%) achieving CR and 10 (40%) PR. Seven were failures. The median follow-up was 21 months (5-26). Eight CR patients remain in CR after 5-21 months. Of 10 PR patients, 3 are in continuous PR without further treatment after 12, 17 and 18 months. Myelosuppression was the most prevalent toxic effect. Although severe granulocytopenia (granulocyte count nadir < 500/microliter) and thrombocytopenia (platelet count nadir < 50,000/microliter) occurred in only 10% and 16% of courses, respectively, slow granulocyte or platelet count recovery caused delay of 40% of the courses. Nine patients (36%) required discontinuation of therapy because of persistent granulocytopenia and/or thrombocytopenia: three after one course, three after 2-4 courses, and three after five courses. Thirteen infectious episodes in 11 patients complicated 11% of courses. Two of 10 patients monitored for the circulating EBV load showed increased viral load. One of these developed aggressive lymphoma. CD4+ lymphocytes declined from a pre-therapy median value of 425/microliter to 141/microliter post-treatment (P = 0.001). Non-hematologic toxicities were rare and mild.

CONCLUSIONS:

The combination of fludarabine with cyclophosphamide and dexamethasone is effective in pretreated advanced-stage low-grade NHL. It may broaden the range of therapeutic options in the salvage treatment of these patients. The main toxicity of this combination is prolonged myelosuppression that may cause treatment delay or withdrawal. The benefit of adding granulocyte colony-stimulating factor, particularly in patients with poor marrow reserve, needs to be investigated.

• Authors: M Lazzarino, E Orlandi, M Montillo, A Tedeschi, G Pagnucco, C Astori, A Corso, E Brusamolino, L Simoncini, E Morra, C Bernasconi
• Journal: Annals of oncology : official journal of the European Society for Medical Oncology (Ann Oncol) Vol. 10 Issue 1 Pg. 59-64 (Jan 1999) ISSN: 0923-7534 [Print] England
• PMID: 10076723 (Publication Type: Clinical Trial, Clinical Trial, Phase II, Journal Article)

Chemical References

• Antineoplastic Agents, Alkylating
• Antineoplastic Agents, Hormonal
• Dexamethasone
• Cyclophosphamide
• Vidarabine
• fludarabine

Topics

• Adult
• Aged
• Antineoplastic Agents, Alkylating (administration & dosage)
• Antineoplastic Agents, Hormonal (administration & dosage)
• Antineoplastic Combined Chemotherapy Protocols (adverse effects, therapeutic use)
• Biopsy
• CD4 Lymphocyte Count (drug effects)
• Cyclophosphamide (administration & dosage)
• Dexamethasone (administration & dosage)
• Disease-Free Survival
• Female
• Humans
• Lymph Nodes (pathology)
• Lymphoma, Non-Hodgkin (drug therapy, mortality, pathology)
• Male
• Middle Aged
• Prognosis
• Remission Induction
• Survival Rate
• Treatment Outcome
• Vidarabine (administration & dosage, analogs & derivatives)