Christine Katlama, MD; Marc-Antoine Valantin, MD; Sophie Matheron, MD; Anne Coutellier, MD; Vincent Calvez, MD; Diane Descamps, MD; Christophe Longuet, MD; Manuela Bonmarchand, MD; Roland Tubiana, MD; Marcio De Sa, MD; Remi Lancar, MSc; Henri Agut, MD; Francoise Brun-Vezinet, MD; Dominique Costagliola, PhD
Katlama C, Valantin M, Matheron S, Coutellier A, Calvez V, Descamps D, et al. Efficacy and Tolerability of Stavudine plus Lamivudine in Treatment-Naive and Treatment-Experienced Patients with HIV-1 Infection. Ann Intern Med. 1998;129:525-531. doi: 10.7326/0003-4819-129-7-199810010-00003
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Published: Ann Intern Med. 1998;129(7):525-531.
A combination of two nucleoside analogues is currently the core of any antiretroviral regimen for HIV-1 infection. Stavudine plus lamivudine has shown an additive effect in vitro, as well as an absence of overlapping toxicity and cross-resistance.
To evaluate the antiviral efficacy of stavudine plus lamivudine in treatment-naive patients and in patients previously treated with other nucleoside reverse transcriptase inhibitors.
Prospective, open-label pilot study.
Three urban clinical centers in Paris.
83 patients with CD4+ cell counts between 50 and 400 cells/mm3 (42 treatment-naive and 41 treatment-experienced patients).
Stavudine, 40 mg twice daily (30 mg twice daily in patients with a body weight ≤ 60 kg), and lamivudine, 150 mg twice daily.
Primary end points for efficacy included changes in plasma viral load and CD4+ cell count at 24 weeks compared with baseline.
Therapy with stavudine plus lamivudine resulted in a median decrease of 1.66 log10 (101.66) (range, −3.04 to −0.79 log10) in plasma HIV-1 RNA; the median increase in CD4+ cell count was 108 cells/mm3 (range, −58 to 406 cells/mm3) at week 24 in treatment-naive patients. In treatment-experienced patients, the median reduction in plasma HIV-1 RNA was 0.55 log10 (range, −2.86 to 0.52 log10), and the median increase in CD4+ cell count was 46 cells/mm3 (range, −188 to 311 cells/mm3). The percentages of patients with less than 3000 HIV-1 RNA copies/mL and less than 400 copies/mL at 24 weeks were, respectively, 57% (95% CI, 41% to 72%) and 26% (CI, 12% to 40%) among treatment-naive patients and 22% (CI, 10% to 38%) and 5% (CI, 1% to 17%) among treatment-experienced patients. Of 82 patients, 14 (17%) experienced grade 3 or 4 toxicity and 2 discontinued therapy because of intolerance toward treatment.
Stavudine plus lamivudine seems to have a potent antiviral effect in treatment-naive and treatment-experienced patients. No major drug-limiting toxicity was found. This two-nucleoside combination should be considered in multidrug therapy for HIV.
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Infectious Disease, HIV.
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