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Impact of cytomegalovirus gastrointestinal disease on the clinical outcomes in patients with gastrointestinal graft-versus-host disease in the era of preemptive therapy.

Authors :
Cho, Byung-Sik
Yahng, Seung-Ah
Kim, Jung-Ho
Yoon, Jae-Ho
Shin, Seung-Hwan
Lee, Sung-Eun
Choi, Su-Mi
Lee, Dong-Gun
Eom, Ki-Seong
Park, Gyeongsin
Kim, Yoo-Jin
Kim, Hee-Je
Lee, Seok
Min, Chang-Ki
Cho, Seok-Goo
Kim, Dong-Wook
Lee, Jong-Wook
Min, Woo-Sung
Park, Chong-Won
Source :
Annals of Hematology. Apr2013, Vol. 92 Issue 4, p497-504. 8p. 2 Diagrams, 4 Charts.
Publication Year :
2013

Abstract

Cytomegalovirus gastrointestinal (CMV-GI) disease in GI graft-versus-host disease (GI-GVHD) has not been properly evaluated in the era of preemptive therapy for CMV infection. We investigated 103 patients with GI-GVHD who underwent endoscopic biopsies with immunohistochemical staining for CMV. All recipients and/or donors were seropositive for CMV and monitored with a strategy of preemptive therapy based on real-time quantitative polymerase chain reaction. Twenty-six patients (25 %) developed CMV-GI disease, especially in HLA-mismatched transplants ( P = 0.023) and with initial gut involvement of GVHD ( P = 0.009). The CMV-GI diseases were diagnosed at follow-up endoscopies ( n = 10, 39 %), comprising 19 % of 52 patients who underwent follow-up endoscopies, as well as initial endoscopies ( n = 16, 61 %), comprising 16 % of all GI-GVHD patients. In seven cases, either at initial ( n = 5) or follow-up endoscopies ( n = 2), CMV-GI disease was diagnosed in the absence of histopathologic evidence for GI-GVHD. Notably, only 11 patients (42 %) had prior CMV DNAemia before the diagnosis of CMV-GI disease, while 12 (46 %) and three (12 %) had concurrent and no CMV DNAemia, respectively. Sixty-five percent of CMV-GI disease was resolved by additional antiviral therapies, but CMV-GI disease ( P = 0.032) as well as severity of GVHD ( P = 0.001) negatively affected GVHD-specific survival. In conclusion, our data demonstrate that CMV-GI disease was a cause of initial or persistent GI manifestations after the initiation of therapy in a considerable proportion of GI-GVHD. These suggest the necessity of novel strategies to reduce CMV-GI disease as well as an effort to confirm CMV with repeated endoscopies. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09395555
Volume :
92
Issue :
4
Database :
Academic Search Index
Journal :
Annals of Hematology
Publication Type :
Academic Journal
Accession number :
85923220
Full Text :
https://doi.org/10.1007/s00277-012-1632-x