Nationwide survey of systemic chronic active EBV infection in Japan in accordance with the new WHO classification

Author:

Yonese Ichiro1,Sakashita Chizuko1,Imadome Ken-Ichi2,Kobayashi Tohru3ORCID,Yamamoto Masahide1,Sawada Akihisa4,Ito Yoshinori5,Fukuhara Noriko6ORCID,Hirose Asao7,Takeda Yusuke8,Makita Masanori9,Endo Tomoyuki10,Kimura Shun-ichi11,Ishimura Masataka12ORCID,Miura Osamu1ORCID,Ohga Shouichi12,Kimura Hiroshi13,Fujiwara Shigeyoshi14,Arai Ayako11516ORCID

Affiliation:

1. Department of Hematology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University (TMDU), Bunkyo-ku, Tokyo, Japan;

2. Department of Advanced Medicine for Infections and

3. Department of Management and Strategy, Clinical Research Center, National Center for Child Health and Development (NCCHD), Setagaya-ku, Tokyo, Japan;

4. Department of Hematology/Oncology, Osaka Women’s and Children’s Hospital, Osaka, Japan;

5. Department of Pediatrics, Nagoya University, Nagoya, Japan;

6. Department of Hematology and Rheumatology, Tohoku University, Sendai, Japan;

7. Department of Hematology, Osaka City University, Osaka, Japan;

8. Department of Hematology, Chiba University Hospital, Chiba, Japan;

9. Department of Hematology, Okayama Medical Center, Okayama, Japan;

10. Department of Hematology, Hokkaido University Hospital, Sapporo, Japan;

11. Department of Hematology, Saitama Medical Center, Jichi Medical University, Saitama, Japan;

12. Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan;

13. Department of Virology, Nagoya University Graduate School of Medicine, Nagoya, Japan;

14. Department of Allergy and Clinical Immunology, NCCHD, Setagaya-ku, Tokyo, Japan;

15. Department of Hematological Therapeutics, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University (TMDU), Bunkyo-ku, Tokyo, Japan; and

16. Division of Hematology and Oncology, Department of Internal Medicine, St. Marianna University School of Medicine, Kawasaki, Japan

Abstract

Abstract Systemic chronic active Epstein-Barr virus infection (sCAEBV) was defined as a T- or NK-cell neoplasm in the 2017 World Health Organization (WHO) classification. To clarify the clinical features of sCAEBV under this classification and review the effects of chemotherapy, we performed a nationwide survey in Japan from 2016 through 2018 of patients with sCAEBV newly diagnosed from January 2003 through March 2016. One hundred cases were evaluated. The patients were aged 1 to 78 years (median, 21) and included 53 males and 47 females. Spontaneous regression was not observed in patients with active disease. In the childhood-onset group (age, <9 years), 78% of the patients were male. In contrast, 85% of the patients in the elderly-onset group (age, >45 years) were female. The prognosis of the childhood-onset group was better than those of the adolescent/adult- and elderly-onset groups. The main chemotherapies used were a combination of cyclosporine A, steroids, and etoposide (cooling therapy) in 52 cases and cyclophosphamide, doxorubicin, vincristine, and prednisolone (CHOP) in 45 cases. The rate of complete response (CR), defined as complete resolution of disease activity, was 17% for cooling therapy and 13% for CHOP. Virological CR was not observed. The 3-year overall survival rates in patients treated with chemotherapy only (n = 20), chemotherapy followed by allogeneic hematopoietic stem cell transplantation (allo-HSCT; n = 47), and allo-HSCT only (n = 12) were 0%, 65%, and 82%, respectively. Distinct characteristics were observed between childhood- and elderly-onset sCAEBV, and they appeared to be different disorders. Chemotherapy is currently insufficient to resolve disease activity and eradicate infected cells. The development of an effective treatment is urgently needed.

Publisher

American Society of Hematology

Subject

Hematology

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