Abstract:The efficacy and safety of preemptive therapy using ganciclovir (GCV) 5 mg/kg once daily for CMV infection after unrelated cord blood transplantation (CBT) were studied. The initial preemptive therapy with GCV 5 mg/kg once daily led to resolution of CMV antigenemia in 25 of 34 patients (74%). In the remaining 9 patients (26%), antigenemia resolved after dose-escalation of GCV or change to foscarnet therapy. Recurrence of antigenemia was seen in 18 patients (53%). A total of 12 patients received the second pree… Show more
“…Among CMV-seropositive recipients who do not receive antiviral prophylaxis, the rate of CMV infection after CBT is 40% to 80%, with one study reporting 100%. 94–98 When patients receive prophylaxis with high-dose valacyclovir after CBT, it does not seem that CBT entails a significantly greater risk of CMV infection and disease than does peripheral blood stem cell or bone marrow transplantation. 89 …”
“…Among CMV-seropositive recipients who do not receive antiviral prophylaxis, the rate of CMV infection after CBT is 40% to 80%, with one study reporting 100%. 94–98 When patients receive prophylaxis with high-dose valacyclovir after CBT, it does not seem that CBT entails a significantly greater risk of CMV infection and disease than does peripheral blood stem cell or bone marrow transplantation. 89 …”
“…One study described successful preemptive treatment with ganciclovir, 98 whereas another combined high-dose valacyclovir prophylaxis with continued monitoring and preemptive therapy. 89 …”
Section: Special Populationsmentioning
confidence: 99%
“…Among CMV-seropositive recipients who do not receive antiviral prophylaxis, the rate of CMV infection after CBT is 40% to 80%, with one study reporting 100%. [94][95][96][97][98] When patients receive prophylaxis with high-dose valacyclovir after CBT, it does not seem that CBT entails a significantly greater risk of CMV infection and disease than does peripheral blood stem cell or bone marrow transplantation. 89 Alemtuzumab is an anti-CD52 monoclonal antibody that results in CD41 and CD81 lymphopenia that can last for up to 9 months after administration.…”
“…Recent studies of adults undergoing HSCT have shown that halving GCV dosage is a promising strategy for preemptive treatment of CMV infection . However, no corresponding studies have been performed in pediatric patients as yet.…”
Half-dose GCV therapy at CMV antigenemia levels <10/200,000 cells is an effective and safe means of preemptively treating pediatric CMV infection after HSCT.
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