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High risk of relapsed disease in patients with NK/T-cell chronic active Epstein-Barr virus disease outside of Asia.

Authors :
Dávila Saldaña, Blachy J
Dávila Saldaña, Blachy J
John, Tami
Bonifant, Challice
Buchbinder, David
Chandra, Sharat
Chandrakasan, Shanmuganathan
Chang, Weni
Chen, Leon
Elfassy, Hannah L
Geerlinks, Ashley V
Giller, Roger H
Goyal, Rakesh
Hagin, David
Islam, Shahidul
Mallhi, Kanwaldeep
Miller, Holly K
Owen, William
Pacheco, Martha
Patel, Niraj C
Querfeld, Christiane
Quigg, Troy
Richard, Nameeta
Schiff, Deborah
Shereck, Evan
Stenger, Elizabeth
Jordan, Michael B
Heslop, Helen E
Bollard, Catherine M
Cohen, Jeffrey I
Dávila Saldaña, Blachy J
Dávila Saldaña, Blachy J
John, Tami
Bonifant, Challice
Buchbinder, David
Chandra, Sharat
Chandrakasan, Shanmuganathan
Chang, Weni
Chen, Leon
Elfassy, Hannah L
Geerlinks, Ashley V
Giller, Roger H
Goyal, Rakesh
Hagin, David
Islam, Shahidul
Mallhi, Kanwaldeep
Miller, Holly K
Owen, William
Pacheco, Martha
Patel, Niraj C
Querfeld, Christiane
Quigg, Troy
Richard, Nameeta
Schiff, Deborah
Shereck, Evan
Stenger, Elizabeth
Jordan, Michael B
Heslop, Helen E
Bollard, Catherine M
Cohen, Jeffrey I
Source :
Blood advances; vol 6, iss 2, 452-459; 2473-9529
Publication Year :
2022

Abstract

Chronic active Epstein-Barr virus (EBV) disease (CAEBV) is characterized by high levels of EBV predominantly in T and/or natural killer cells with lymphoproliferation, organ failure due to infiltration of tissues with virus-infected cells, hemophagocytic lymphohistiocytosis, and/or lymphoma. The disease is more common in Asia than in the United States and Europe. Although allogeneic hematopoietic stem cell transplantation (HSCT) is considered the only curative therapy for CAEBV, its efficacy and the best treatment modality to reduce disease severity prior to HSCT is unknown. Here, we retrospectively assessed an international cohort of 57 patients outside of Asia. Treatment of the disease varied widely, although most patients ultimately proceeded to HSCT. Though patients undergoing HSCT had better survival than those who did not (55% vs 25%, P < .01), there was still a high rate of death in both groups. Mortality was largely not affected by age, ethnicity, cell-type involvement, or disease complications, but development of lymphoma showed a trend with increased mortality (56% vs 35%, P = .1). The overwhelming majority (75%) of patients who died after HSCT succumbed to relapsed disease. CAEBV remains challenging to treat when advanced disease is present. Outcomes would likely improve with better disease control strategies, earlier referral for HSCT, and close follow-up after HSCT including aggressive management of rising EBV DNA levels in the blood.

Details

Database :
OAIster
Journal :
Blood advances; vol 6, iss 2, 452-459; 2473-9529
Notes :
application/pdf, Blood advances vol 6, iss 2, 452-459 2473-9529
Publication Type :
Electronic Resource
Accession number :
edsoai.on1377980297
Document Type :
Electronic Resource