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Lookup NU author(s): Dr Penelope Taylor, Professor Stephen Proctor
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Chlorambucil has been used for many years for the treatment of low-grade B-cell lymphoproliferative disorders, including chronic lymphocytic leukaemia and low-grade non-Hodgkin's lymphoma. There is evidence in the literature that increasing the dose of chlorambucil produces better results than 'standard' doses in terms of response rates and overall survival. There is also evidence that this approach may be at least as effective as the use of fludarabine, as well as being very much less expensive. We describe a high-dose chlorambucil (HDC) regimen, which involves a sustained but intermittent dose of chlorambucil, i.e. 30 mg/d for 4 d per week for 4 weeks, followed by a further four courses at fortnightly intervals for 8 weeks (a total of eight 4-d courses) given as a single drug over an initial 12-week period. The outcome of treatment in previously treated and untreated patients was excellent, with a median time to treatment failure of 33 months for the patient cohort overall and for previously treated and chemotherapy-naive patients of 13 and 104 months respectively. In patients previously treated with fludarabine, 78% had a response. Autoimmune haemolytic anaemia was reversed in one patient. Toxicity, both haematological and other, was minimal. We propose that escalated-dose chlorambucil regimens should be compared with fludarabine in randomized controlled trials, rather than 'standard' lower dose protocols.
Author(s): Summerfield GP, Taylor PRA, Mounter PJ, Proctor SJ
Publication type: Article
Publication status: Published
Journal: British Journal of Haematology
Year: 2002
Volume: 116
Issue: 4
Pages: 781-786
Print publication date: 01/03/2002
ISSN (print): 0007-1048
ISSN (electronic): 1365-2141
URL: http://dx.doi.org/10.1046/j.0007-1048.2002.03362.x
DOI: 10.1046/j.0007-1048.2002.03362.x
PubMed id: 11886381
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