Abstract | PURPOSE: PATIENTS AND METHODS: We treated eight patients with cladribine 0.1 mg/kg/d for 7 days by continuous infusion or 0.14 mg/kg/d over 2 hours for 5 days, every 28 to 35 days, for a median of three courses (range, two to five). There were five men and three women, with a median age of 62 years and a median pretreatment duration of 6 months; four patients were previously untreated. RESULTS: All eight patients were assessable: five achieved a complete response with a median response duration of 14 months (range, 1+ to 55+), and three achieved a partial response with a median duration of 3 months (range, 1 to 3). Of four patients who achieved a complete response and in whom a peripheral-blood immunophenotypic analysis was performed, two had no circulating B-PLL cells and one had no residual disease on Southern blot analysis. Myelosuppression and infection were the major toxicities: three patients developed grade 3 or 4 myelosuppression, four had bacterial infections, and two had herpes zoster infections. CONCLUSION: In this small study of patients with de novo B-PLL, cladribine was an active agent that induced a high overall and complete response rate. These results require confirmation in larger numbers of B-PLL patients.
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Authors | A Saven, T Lee, M Schlutz, A Jacobs, D Ellison, R Longmire, L Piro |
Journal | Journal of clinical oncology : official journal of the American Society of Clinical Oncology
(J Clin Oncol)
Vol. 15
Issue 1
Pg. 37-43
(Jan 1997)
ISSN: 0732-183X [Print] United States |
PMID | 8996122
(Publication Type: Journal Article)
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Chemical References |
- Antineoplastic Agents
- Cladribine
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Topics |
- Adult
- Aged
- Aged, 80 and over
- Antineoplastic Agents
(adverse effects, therapeutic use)
- Cladribine
(adverse effects, therapeutic use)
- Drug Administration Schedule
- Female
- Humans
- Leukemia, Prolymphocytic
(drug therapy, microbiology, pathology)
- Male
- Middle Aged
- Neoplasm Staging
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