Third International Congress

Drug Therapy in HIV Infection


3-7 November 1996
Glasgow, UK


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EFFICACY OF DIFFERENT ANTIVIRAL TREATMENTS IN CYTOMEGALOVIRUS (CMV) NEUROLOGICAL COMPLICATIONS: EVALUATION BY QUANTITATIVE POLYMERASE CHAIN REACTION (PCR) ON CEREBROSPINAL FLUID (CSF).

P. Cinque1, E. Pisa2, S. Racca1, S. Bossolasco1, R. Marenzi1, A. Lazzarin1, A. Linde3
1Infectious Diseases Dept., San Raffaele Hospital, Milan, Italy; 2AB Sangtec Medical, Bromma, Sweden; 3Virology Dept., Swedish Institute for Infectious Disease Control, Stockholm, Sweden

Int Cong Drug Therapy HIV 1996 Nov 3-7;3:Abstract No. OP3.3br /> AIDS 1996, Vol. 10 (Suppl. 2);S12


The efficacy of various antiviral treatment regimens in CMV neurological complications was evaluated using a quantitative PCR assay for the detection of CMV DNA in CSF.

30 HIV-infected patients with CMV encephalitis (CMV-E, n=26) or polyradiculomyelitis (CMV-P, n=4), received ganciclovir (GCV, 10 mg/Kg/day), foscarnet (PFA, 180 mg/Kg/day), or a combination of the two drugs. After 3 weeks of treatment, the majority of the patients with CMV-E received half-dose maintenance therapy, while 2 patients with CMV-P continued with full dose GCV.

The table shows the CMV DNA titres in the CSF (genome equivalents / ml ± S.D.) before and after 3 weeks of full dose treatment.

Treatment baseline week 3
GCV (CMV-E, n=16) 435,560 ± 1,047,920 55,680 ± 115,240
PFA (CMV-E, n=7) 642,720 ± 1,513,920 444,840 ± 714,160
GCV+PFA (CMV-E, n=3) 630,960 ± 521,348 42,270 ± 98,542
GCV (CMV-P, n=4) 1,153,040 ± 116,520 66,360 ± 77,030

Clinical neurological conditions improved in 6/26 patients with CMV-E, without apparent correlation with the drugs received, and in all the 4 patients with CMV-P. After 4 weeks of maintenance therapy, CSF CMV DNA titres were elevated up to baseline levels in all the 6 evaluable patients with CMV-E, whereas they were further decreased after 5-16 weeks of full dose GCV in both patients with CMV-P. Autopsy examination confirmed CMV-E in 9/10 patients examined.

In most of patients full dose GCV or/and PFA for 3 weeks is effective in reducing CMV replication in the nervous system. The clinical neurological response, however, is poor in most of the patients with CMV-E.

Presenting author: P. Cinque

1996-11-03
OP3.3


Originally published in AIDS Volume 10, Supplement 2 and hosted with permission of the publisher Lippincott Williams & Wilkins, 250 Waterloo Road, London, SE1 8RD, UK. Tel: +44 (0)20 7981 0700 Fax: +44 (0) 7981 0701

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