PILOT-STUDY OF ZIDOVUDINE-LAMIVUDINE COMBINATION THERAPY IN VERTICALLY HIV-INFECTED ANTIRETROVIRAL-NAIVE CHILDREN

Objective: To examine tolerance and efficacy of a zidovudine plus lami vudine combination in HIV-infected children without previous exposure to antiretroviral drugs. Methods: Thirteen vertically infected childre n (aged 4 months to 10 years) were treated with zidovudine (approximat ely 100 mg/m(2) three times daily) and lamivudine (4 mg/kg twice daily ). CD4 T-cell count, plasma HIV RNA concentration, complete blood coun t and blood chemistry profile were monitored before treatment and at m onths 1, 3 and 6. Results: In general, treatment was well tolerated. O ne child developed slight neutropenia in the presence of antineutrophi l antibodies. CD4 cell count increased from 851 +/- 621 x 10(6)/l at b aseline to 1073 +/- 945 x 10(6)/l at month 3 (P < 0.05) and to 1133 +/ - 728 x 10(6)/l at month 6 (P = 0.01). CD4+ cell count increased in 10 patients after 3 months and in 11 patients treated for 6 months. One child showed a continuous decrease of CD4 cells despite treatment. Bef ore treatment the plasma HIV RNA concentration was elevated in nine ch ildren (> 4.0 log(10) copies/ml) and decreased in all of them: by mont h 1, the mean reduction was -1.16 log(10) copies/ml; by month 3, -1.38 log(10) copies/ml; and by month 6, -1.53 log(10) copies/ml compared w ith baseline. However, one child showed steadily increasing viral load from 2.7 log(10) copies/ml to a maximum of 4.52 log(10) copies/ml, su rprisingly in association with increasing numbers of CD4 cells. This c hild was switched to a new combination regimen after 6 months of treat ment. Plasma HIV RNA levels below limit of detection were reached in s ix patients: after 1 month of treatment in one patient, after 3 months in five patients, and after 6 months in six patients. There was a mea n reduction of viral load from 4.56 log(10) +/- 4.63 log(10) copies/ml (n = 13) to 3.8 log(10) +/- 3.9 log(10) copies/ml (P < 0.05; n = 9) a fter 1 month, to 3.64 log(10) +/- 3.88 log(10) copies/ml (P < 0.01; n = 13) after 3 months, and to 3.64 log(10) +/- 3.95 log(10) copies/ml a fter 6 months of treatment (P < 0.001; n = 13). Conclusions: This pilo t study demonstrates the feasibility of zidovudine-lamivudine combinat ion in children not previously exposed to antiretroviral drugs. This p romising combination should therefore be evaluated in larger trials. ( C) 1998 Rapid Science Ltd.