Ja. Carton et al., Cytomegalovirus antigenemia surveillance in the treatment of cytomegalovirus disease in AIDS patients, J CHEMOTHER, 11(3), 1999, pp. 195-202
Objective: Surveillance of quantitative cytomegalovirus (CMV) antigenemia a
mong AIDS patients with CMV treated complications in order to determine its
value in assessing the response to treatment and survival.
Methods: A longitudinal follow-up of antigenemia measurement at diagnosis,
after induction therapy with ganciclovir or foscarnet, and every 3 months d
uring maintenance therapy was carried out in 25 patients with CMV retinitis
and in 8 with extraocular CMV disease. Positive antigenemia was defined as
the presence of any amount of immunofluorescent pp65-positive leukocytes /
10(5) cells.
Results: Mean antigenemia values were: 77+/-148 /10(5) leukocytes at retini
tis diagnosis; 45+/-114 after induction therapy; and 7+/-18 and 1.5+/-4 aft
er 6 months and one year of therapy, respectively. Patients achieving undet
ectable antigenemia increased from 44% at baseline to 68% at postinduction
and 80% during follow-up, Seven patients (28%) who remained free of relapse
s presented significant minor baseline antigenemias and became negative aft
er induction therapy. Patients with extraocular disease showed erratic anti
genemia values and absent therapeutic response. CMV blood cultures before a
nd after induction therapy were positive in 39% and 21% of patients, respec
tively. Kaplan-Meier analysis revealed a significantly longer survival for
patients with retinitis when compared to those with extraocular complicatio
ns, and for patients with negative antigenemia after induction in compariso
n with those who failed to achieve it.
Conclusions: Low basal antigenemia and antigenemia clearance after inductio
n therapy are variables directly related to good response to treatment and
survival. Continuous surveillance of antigenemia during treatment could per
mit designing of individual strategies to obtain a better response.