Massimo Marroni, MD; Paolo Gresele, MD, PhD; Giuseppe Landonio, MD; Adriano Lazzarin, MD; Massimo Coen, MD; Roberta Vezza, PharmD; Marina Silva Sinnone, MD; Enrico Boschetti, MD; Anna Maria Nosari, MD; Giuliano Stagni, MD; Giuseppe Giorgio Nenci, MD; Sergio Pauluzzi, MD
Marroni M, Gresele P, Landonio G, Lazzarin A, Coen M, Vezza R, et al. Interferon-Alpha Is Effective in the Treatment of HIV-1–Related, Severe, Zidovudine-Resistant Thrombocytopenia: A Prospective, Placebo-controlled, Double-Blind Trial. Ann Intern Med. 1994;121:423-429. doi: 10.7326/0003-4819-121-6-199409150-00005
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Published: Ann Intern Med. 1994;121(6):423-429.
To determine the effect of interferon-α for severe, zidovudine-resistant, HIV-1–related thrombocytopenia.
Prospective, randomized, double-blind, placebo-controlled, multicenter, crossover trial.
Outpatient clinics in Central Northern Italy.
15 sequential patients positive for HIV-1 with platelet counts less than 25 × 109/L who were refractory to 1 month of full-dose (1000 mg/d) zidovudine.
Interferon-α (3 million units) or placebo (1 mL saline) three times a week subcutaneously for 4 weeks, followed by a 4-week washout period. Patients were then switched to the alternative treatment for the next 4 weeks, followed by another 4 weeks of washout, and they were randomly assigned to either sequence of treatment. Patients received zidovudine (200 mg three times daily) throughout the study.
The primary end point was the platelet count (measured weekly). Secondary end points were qualitative assessment of the platelet response; bleeding time; p24 antigen in serum; CD4/CD8 counts; β2-microglobulin in serum; and platelet-associated IgG.
Interferon-α significantly increased platelet counts in the 12 patients who completed the study (baseline level, 15.6 ± 7.1 × 109/L; after 4 weeks of interferon-α therapy, 82.2 ± 52.2 × 109/L). The estimated increase in the platelet count after interferon-α compared with placebo was 60.0 × 109/L (95% CI, 23.2 to 96.8 × 109/L). The increase was already statistically significant after 3 weeks (66.6 ± 49.7 × 109/L) and remained significantly increased 1 week after discontinuing interferon-α therapy (58.2 ± 45.0 × 109/L). Placebo did not modify the platelet count. The bleeding time was significantly shortened by interferon-α. Four of 12 patients who had more serious alterations of some measures reflecting disease severity did not respond to interferon-α. No relevant side effects were observed.
Interferon-α is a safe and effective treatment for zidovudine-resistant, HIV-related thrombocytopenia.
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Hematology/Oncology, HIV, Infectious Disease, Platelet Disorders.
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