| Literature DB >> 30788725 |
Ryu Yanagaisawa1,2,3, Kazuyuki Matsuda4, Shouichi Ohga5, Hirokazu Kanegane6, Akira Morimoto7, Yasuhiro Okamoto8, Akira Ohara9, Keitaro Fukushima10, Manabu Sotomatsu11, Keiko Nomura12, Akiko M Saito3, Keizo Horibe3, Eiichi Ishii13, Yozo Nakazawa14.
Abstract
Epstein-Barr virus (EBV)-associated hemophagocytic lymphohistiocytosis (HLH) is highly prevalent in Japan. To date, no standard treatment for EBV-HLH has been established owing to the diversity in treatment response and the difficulty in assessing prognostic factors. The present prospective study recruited 27 children with EBV-HLH who were also part of the HLH-2004 study. EBV load in the peripheral blood was monitored at diagnosis and 2, 4, and 8 weeks after treatment initiation. Additionally, T-cell receptor (TCR) clonality and other laboratory data were evaluated. TCR clonality was positive in 14 patients at diagnosis. Seven of 27 patients experienced recurrences after treatment. No correlation was noted among any clinical data at diagnosis of patients with and without recurrence. However, the recurrence rate was significantly higher in patients aged < 2 years and/or those with a high plasma EBV load of > 103 copies/mL 2 weeks after treatment than that in patients without these factors. These findings suggest that a younger age or a high EBV load in plasma at the early phase of treatment is a factor predicting a recurrence and helps guide the intensity of subsequent treatment phases for children with EBV-HLH.Entities:
Keywords: EBV DNA; HLH-2004 protocol; Hemophagocytic lymphohistiocytosis
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Year: 2019 PMID: 30788725 DOI: 10.1007/s12185-019-02612-2
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.490