Pulsed intravenous high-dose dexamethasone in adults with chronic idiopathic thrombocytopenic purpura

Citation
R. Stasi et al., Pulsed intravenous high-dose dexamethasone in adults with chronic idiopathic thrombocytopenic purpura, BL CELL M D, 26(6), 2000, pp. 582-586
Citations number
12
Language
INGLESE
art.tipo
Article
Categorie Soggetti
Cardiovascular & Hematology Research
Journal title
BLOOD CELLS MOLECULES AND DISEASES
ISSN journal
1079-9796 → ACNP
Volume
26
Issue
6
Year of publication
2000
Pages
582 - 586
Database
ISI
SICI code
1079-9796(200012)26:6<582:PIHDIA>2.0.ZU;2-I
Abstract
The role of pulsed high-dose dexamethasone (DXM) in the treatment of patien ts with chronic idiopathic thrombocytopenic purpura (ITP) is still uncertai n. Following an early report in which it was described as an effective and well-tolerated treatment with a sustained platelet response in 100% of case s, a number of subsequent studies have failed to confirm such favorable res ults. As all these studies were conducted on small numbers of patients, we investigated further the effectiveness and side effects of this therapeutic modality in a larger cohort. Thirty-two patients with chronic ITP were sch eduled to receive six monthly courses of intravenous DXM at the dose of 40 mg/day for 4 consecutive days. All patients had ITP that had been resistant to between two and five different therapeutic regimens, including 9 patien ts who had already failed splenectomy. AIL patients had to be seen 2 weeks after each cycle to asses their response as well as secondary effects. Thre e patients failed to respond and clinically required other therapy. Thirtee n patients (41%) had a partial (platelet count between 50 and 100 x 10(9)/l iter) or complete (platelet count >100 x 10(9)/liter) response to treatment , responses being mostly transient. Responses were observed early during th e course of treatment, usually right after the first cycle of DXM. There we re no late responses. Side effects were mild and did not require discontinu ation of treatment. No clinical or laboratory parameter was found to predic t treatment outcome. We conclude that high-dose DXM has a limited effect in patients with chronic ITP. Novel approaches and controlled multicenter tri als may help identify new therapeutic strategies for this disease. (C) 2000 Academic Press.