Risk factors and clinical features of cytomegalovirus disease in children receiving anticancer chemotherapy

Mi Seon Han, Hoan Jong Lee, Hyunju Lee, Young June Choe, Ji Won Lee, Hyoung Jin Kang, Kyung Duk Park, Hee Young Shin, Hyun Joo Jung, Eun Hwa Choi

Research output: Contribution to journalArticlepeer-review

11 Scopus citations

Abstract

This study was conducted to identify risk factors for cytomegalovirus (CMV) infection and demonstrate the spectrum of CMV disease in children receiving anticancer chemotherapy without hematopoietic stem cell transplantation (HSCT). A total of 289 children who received chemotherapy and were tested for CMV infection were included in the study. CMV antigenemia and DNAemia were determined by identifying the pp65 antigen in leukocytes and performing real-time PCR. CMV disease was diagnosed by tissue biopsy, culture, or ophthalmic examination. Of the 289 children, CMV infection was demonstrated in 46 patients (15.9%). Young age at cancer diagnosis was the risk factor for CMV infection by multivariate analysis (7mo vs. 7 y, P<0.001). Among 46 children with CMV infection, 10 (21.7%) were diagnosed with CMV disease; hepatitis (n=4), retinitis (n=3), hepatitis and pneumonia (n=2), and hepatitis and retinitis (n=1). The age of the patients with CMV disease was significantly younger than those without (3 vs. 16 mo, P=0.023). Retinoblastoma and neuroblastoma were the 2 most common underlying malignancies. There were 2 fatal cases associated with CMV disease, including 1 who died of CMV pneumonia. The findings of this study demonstrated significant morbidity of CMV infection and disease in young children during the course of chemotherapy without HSCT.

Original languageEnglish
Pages (from-to)e113-e119
JournalJournal of Pediatric Hematology/Oncology
Volume38
Issue number3
DOIs
StatePublished - 13 Apr 2016
Externally publishedYes

Keywords

  • Chemotherapy
  • Children
  • Cytomegalovirus disease
  • Neutropenia

Fingerprint

Dive into the research topics of 'Risk factors and clinical features of cytomegalovirus disease in children receiving anticancer chemotherapy'. Together they form a unique fingerprint.

Cite this