DELTA - A RANDOMIZED DOUBLE-BLIND CONTROLLED TRIAL COMPARING COMBINATIONS OF ZIDOVUDINE PLUS DIDANOSINE OR ZALCITABINE WITH ZIDOVUDINE ALONE IN HIV-INFECTED INDIVIDUALS
V. Aber et al., DELTA - A RANDOMIZED DOUBLE-BLIND CONTROLLED TRIAL COMPARING COMBINATIONS OF ZIDOVUDINE PLUS DIDANOSINE OR ZALCITABINE WITH ZIDOVUDINE ALONE IN HIV-INFECTED INDIVIDUALS, Lancet, 348(9023), 1996, pp. 283-291
Background Because the benefits of zidovudine (AZT) in HIV-infected in
dividuals are small and do not last long the Delta trial was designed
to test whether combinations of zidovudine with didanosine (ddI) or za
lcitabine (ddC) were more effective than AZT alone in extending surviv
al and delaying disease progression. Methods The trial was randomised,
double blind, and international. 3207 participants were allocated to
either AZT (600 mg per day) alone (1055), AZT plus ddl (400 mg per day
) (1080), or AZT plus ddC (2.25 mg per day) (1072), Participants eithe
r had symptoms of HIV disease (if AIDS, with a CD4 cell count of > 50
x 10(6)/L) or a CD4 count of less than 350 x 10(6)/L; 2124 had not had
zidovudine before (Delta 1) and 1083 had for at least 3 months (Delta
2). Findings Over a median follow-up of 30 months, 699 participants d
ied, and 936 of the 2765 without AIDS at entry developed AIDS or died,
In participants who had not had AZT before, both combination regimens
had substantial benefits in terms of survival (regardless of disease
stage at entry); a relative reduction in mortality of 42%, compared to
AZT alone (95% CI 25% to 55%), for AZT plus ddl and of 32% (95% CI 22
% to 47%) for AZT plus ddC. In participants who had had AZT before, th
e addition of ddl improved survival (p=0.05; relative reduction 23% [9
5% CI 0% to 41%]) but there was no direct evidence of benefit from the
addition of ddC (p=0.47; relative reduction 9% [95% CI-17% to 29%]).
The overall difference in survival between the treatment groups was si
gnificant (p<0.0001; a relative reduction in mortality, compared to AZ
T alone, of 33% (95% CI 20% to 44%) for AZT plus ddl and 21% (95% CI 6
% to 34%) for AZT plus ddC), Benefit in terms of disease progression w
as seen mainly in participants not previously treated with AZT and ove
rall, There was no unexpected toxicity from the combination treatments
. Interpretation Initiation of treatment with combinations of AZT plus
ddl or ddC prolongs life and delays disease progression compared with
AZT alone. The addition of ddl to participants already treated with A
ZT also improves survival, although the benefit appears less.