Risk-adapted preemptive therapy for cytomegalovirus disease after allogeneic stem cell transplantation: A single-center experience in Korea

Su Mi Choi, Dong Gun Lee, Jung Hyun Choi, Jin Hong Yoo, Yoo Jin Kim, Hee Park Sun, Sun Nam Park, Chang Ki Min, Seok Lee, Hee Je Kim, Dong Wook Kim, Jong Wook Lee, Woo Sung Min, Wan Shik Shin, Chun Choo Kim

Research output: Contribution to journalArticlepeer-review

24 Scopus citations

Abstract

Cytomegalovirus (CMV) remains a major cause of infection in recipients of hematopoietic stem cell transplants (HSCT) and results in significant mortality and morbidity. We present the results of CMV pp65 antigenemia-guided, risk-adapted preemptive therapy aimed at preventing CMV disease in allogeneic HSCT. Preemptive ganciclovir treatment was started when more than 5 CMV antigen-positive cells were detected in the low-risk group (with grade 0-I acute GVHD and matched related HSCT) and when any antigen-positive cells were seen in the high-risk group (with grade II-IV acute GVHD or matched unrelated HSCT). At least 1 episode of antigenemia was observed in 53 (59.6%) of 89 patients before day 100, and preemptive therapy was performed in 33 patients. CMV disease occurred in 6 patients (5 in the high-risk group and 1 in the low-risk group), and late CMV disease developed in 4 patients. Only 1 patient died of CMV pneumonitis before day 100. Neutropenia was observed in 51.5% of ganciclovir-treated patients, and coinfection/superinfection was observed in 42.4%. A strategy of ganciclovir treatment focusing on patients at higher risk could reduce the toxicity from the antiviral drug and be cost-effective. Extended surveillance for CMV disease using more sensitive diagnostic methods is necessary in high-risk patients.

Original languageEnglish
Pages (from-to)69-74
Number of pages6
JournalInternational Journal of Hematology
Volume81
Issue number1
DOIs
StatePublished - Jan 2005

Keywords

  • CMV antigenemia
  • Cytomegalovirus
  • Ganciclovir
  • Preemptive therapy

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