Objectives: To compare, in a community-based therapeutic setting, the safety, tolerance, and efficacy of combination therapy with recombinant interferon-α2b (rIFNα2b) and zidovudine (ZDV) to ZDV monotherapy. Design: Open-label, two-armed, randomized study. Patients and Methods: Asymptomatic or minimally symptomatic HIV-infected adults without an AIDS-defining illness, a CD4 count of 200 to 500 cells/μl, and ≤6 months of prior ZDV therapy received ZDV 100 mg orally five times daily. Patients randomized to rIFN-α2b received 3 million IU subcutaneously three times weekly for 2 weeks and 5 million IU three times weekly thereafter. The groups were compared with respect to adverse events (AEs), dosing modifications, treatment discontinuation, clinical endpoints and changes in CD4 count. A virology substudy compared the treatments with respect to HIV viral load and development of ZDV resistance. Results: Between October, 1991 and January, 1993, 139 patients were randomized to combination therapy and 117 to ZDV alone. Of AEs reported at any grade, fatigue, myalgias, and sweating occurred significantly more often with combination therapy (p < .001). Study subjects receiving combination therapy showed modest but significantly greater weight loss (p = .0001), a significantly higher frequency of any abnormal laboratory test result (p = .002), neutropenia (p = .002), and leukopenia (p = .02), and also required dosage reduction for hematologic toxicity significantly more often (p < .05) than those in the ZDV monotherapy arm. No statistically significant differences were found between the groups with respect to development of specific AIDS-defining events, overall event rate, time to events, or change in performance status or CD4+ counts, or percentages or development of ZDV resistance. Viral burden, reflected by serum p24 antigen and quantitative peripheral blood mononuclear cell (PBMC) microcultures, was greater at baseline in the combination therapy group. Baseline SI phenotype predicted progression to AIDS (p = .004, χ2), whereas intermediate susceptibility to ZDV predicted development of ZDV resistance (p < .005, χ2). The annual rate of development of phenotypic resistance to ZDV was 16.8% and was not affected by administration of rIFN-α2b. Conclusions: At the doses and schedule used in this study, the combination of ZDV with rIFN- α2b was not therapeutically superior to ZDV alone and was less well tolerated. The addition of rIFN-α2b to ZDV did not prevent or delay the development of ZDV resistance.
|Original language||English (US)|
|Number of pages||10|
|Journal||Journal of Acquired Immune Deficiency Syndromes and Human Retrovirology|
|State||Published - Mar 1 1999|
- Drug resistance
- HIV infection