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

Author:

Dávila Saldaña Blachy J.12ORCID,John Tami3ORCID,Bonifant Challice4ORCID,Buchbinder David56,Chandra Sharat7ORCID,Chandrakasan Shanmuganathan8ORCID,Chang Weni9ORCID,Chen Leon1ORCID,Elfassy Hannah L.10ORCID,Geerlinks Ashley V.7,Giller Roger H.11ORCID,Goyal Rakesh12ORCID,Hagin David13ORCID,Islam Shahidul14,Mallhi Kanwaldeep15ORCID,Miller Holly K.16,Owen William17ORCID,Pacheco Martha18,Patel Niraj C.19,Querfeld Christiane20ORCID,Quigg Troy21ORCID,Richard Nameeta22,Schiff Deborah2324ORCID,Shereck Evan25ORCID,Stenger Elizabeth8ORCID,Jordan Michael B.7,Heslop Helen E.26ORCID,Bollard Catherine M.12ORCID,Cohen Jeffrey I.27

Affiliation:

1. Department of Pediatrics, George Washington University, Washington, DC;

2. Cell Enhancement and Technologies for Immunotherapy, Children’s National Hospital, Washington, DC;

3. Department of Pediatrics, Center for Cell and Gene Therapy, Texas Children’s Hospital/Baylor College of Medicine, Houston, TX;

4. Department of Pediatrics, University of Michigan, Ann Arbor, MI;

5. Department of Hematology, Children's Hospital of Orange County, Orange, CA;

6. Department of Pediatrics, University of California at Irvine, Orange, CA;

7. Division of Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH;

8. Aflac Cancer & Blood Disorders Center, Children’s Healthcare of Atlanta/Emory University, Atlanta, GA;

9. Department of Pediatrics, Hasbro Children’s Hospital, The Warren Alpert Medical School of Brown University, Providence, RI;

10. Sacrée-Coeur of Montréal Hospital, University of Montréal, Montréal, QC, Canada;

11. Pediatric Bone Marrow Transplant & Cellular Therapeutics Program, Children’s Hospital Colorado/University of Colorado School of Medicine, Aurora, CO;

12. Division of Hematology, Oncology, and Blood and Marrow Transplant, Children’s Mercy Kansas City, Kansas City, MO;

13. Allergy and Clinical Immunology Unit, Department of Medicine, Tel Aviv Sourasky Medical Center and Sackler Faculty of Medicine, University of Tel Aviv, Tel Aviv, Israel;

14. Department of Haematology, Waikato Hospital, Hamilton, New Zealand;

15. Fred Hutchinson Cancer Research Center, University of Washington, Seattle, WA;

16. Phoenix Children’s Hospital, Phoenix, AZ;

17. Children's Cancer and Blood Disorders Center, Children's Hospital of the King's Daughters, Norfolk, VA;

18. Pediatric Hematology/Oncology, Children's Health/University of Texas Southwestern, Dallas, TX;

19. Levine Children’s Hospital, Atrium Health, Charlotte, NC;

20. Division of Dermatology and Toni Stephenson Lymphoma Center, City of Hope and Beckman Research Institute, Duarte, CA;

21. Pediatric Blood and Marrow Transplantation Program, Methodist Children’s Hospital, San Antonio, TX;

22. Children’s Cancer and Blood Disorders Program, Randall Children’s Hospital at Legacy Emanuel, Portland, OR;

23. Department of Pediatrics, University of California San Diego, La Jolla, CA;

24. Division of Hematology-Oncology, Rady Children’s Hospital, San Diego, CA;

25. Division of Pediatric Hematology/Oncology, Oregon Health and Science University, Portland, OR;

26. Center for Cell and Gene Therapy, Baylor College of Medicine, Houston Methodist Hospital and Texas Children’s Hospital, Houston, TX; and

27. Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD

Abstract

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.

Publisher

American Society of Hematology

Subject

Hematology

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