TY - JOUR
T1 - Registry data analysis of hematopoietic stem cell transplantation on systemic chronic active Epstein–Barr virus infection patients in Japan
AU - Yamamoto, Masahide
AU - Sato, Maho
AU - Onishi, Yasushi
AU - Sasahara, Yoji
AU - Sano, Hideki
AU - Masuko, Masayoshi
AU - Nakamae, Hirohisa
AU - Matsuoka, Ken ichi
AU - Ara, Takahide
AU - Washio, Kana
AU - Onizuka, Makoto
AU - Watanabe, Kenichiro
AU - Takahashi, Yoshiyuki
AU - Hirakawa, Tsuneaki
AU - Nishio, Miwako
AU - Sakashita, Chizuko
AU - Kobayashi, Tohru
AU - Sawada, Akihisa
AU - Ichinohe, Tatsuo
AU - Fukuda, Takahiro
AU - Hashii, Yoshiko
AU - Atsuta, Yoshiko
AU - Arai, Ayako
N1 - Funding Information:
The authors thank Dr Shintaro Iwamoto of the National Center for Child Health and Development, Japan for supervising the statistical analyses. The authors thank Ayako Komoto, an assistant supported by funding from the Japanese Agency for Medical Research and Development (AMED), for her excellent editorial support during manuscript preparation. This study was supported by grants from the Practical Research Project for Rare/Intractable Diseases (18ek0109334h0001, 19ek0109334h0002, 20ek0109334h0003, and 21ek0109334h0004) of the AMED.
Funding Information:
The authors thank Dr Shintaro Iwamoto of the National Center for Child Health and Development, Japan for supervising the statistical analyses. The authors thank Ayako Komoto, an assistant supported by funding from the Japanese Agency for Medical Research and Development (AMED), for her excellent editorial support during manuscript preparation. This study was supported by grants from the Practical Research Project for Rare/Intractable Diseases (18ek0109334h0001, 19ek0109334h0002, 20ek0109334h0003, and 21ek0109334h0004) of the AMED.
Publisher Copyright:
© 2022 Wiley Periodicals LLC.
PY - 2022/6/1
Y1 - 2022/6/1
N2 - The effects of allogeneic hematopoietic stem cell transplantation (allo-HSCT) on systemic chronic active Epstein–Barr virus infection (sCAEBV) are yet to be analyzed in a large number of patients. Using the Japanese registry database, Transplant Registry Unification Management Program, we investigated the outcomes of 102 sCAEBV patients who underwent allo-HSCT. The median age at HSCT was 21 years, and the three-year overall survival (3-year OS) rate was 72.5%. Of the 90 patients whose viral load after allo-HSCT was evaluated, 56 (62.2%) achieved a virological complete response, defined by the complete resolution of disease activity with a significant decrease in EBV-DNA in peripheral blood. The multivariate Cox proportional hazard model indicated that advanced age, in adolescents and young adults (AYA) (age, 15–39) and adults (age, ≥40 years) was a risk factor of poor OS. The hazard ratios (HRs) of the AYA and adult groups were 10.87 (95% confidence interval [CI]: 1.98–59.56, p =.006) and 15.93 (95% CI: 2.45–103.8, p =.004), respectively. Disease activity (HR 5.74), elevated soluble IL-2 receptor (sIL-2R) (≥ median, 691 U/mL) at HSCT (HR 6.93), and conditioning without radiotherapy (HR 3.53) were also independently associated with poor survival. Notably, 79% of radiotherapy doses were less than 6 Gy. Regardless of the presence of hemophagocytic lymphohistiocytosis, the group with a high sIL-2R level (≥2000 U/mL) showed a poorer prognosis. Although allo-HSCT is the only curative therapy for sCAEBV, treatment strategies need to be improved for high-risk patients, especially those with high levels of sIL-2R.
AB - The effects of allogeneic hematopoietic stem cell transplantation (allo-HSCT) on systemic chronic active Epstein–Barr virus infection (sCAEBV) are yet to be analyzed in a large number of patients. Using the Japanese registry database, Transplant Registry Unification Management Program, we investigated the outcomes of 102 sCAEBV patients who underwent allo-HSCT. The median age at HSCT was 21 years, and the three-year overall survival (3-year OS) rate was 72.5%. Of the 90 patients whose viral load after allo-HSCT was evaluated, 56 (62.2%) achieved a virological complete response, defined by the complete resolution of disease activity with a significant decrease in EBV-DNA in peripheral blood. The multivariate Cox proportional hazard model indicated that advanced age, in adolescents and young adults (AYA) (age, 15–39) and adults (age, ≥40 years) was a risk factor of poor OS. The hazard ratios (HRs) of the AYA and adult groups were 10.87 (95% confidence interval [CI]: 1.98–59.56, p =.006) and 15.93 (95% CI: 2.45–103.8, p =.004), respectively. Disease activity (HR 5.74), elevated soluble IL-2 receptor (sIL-2R) (≥ median, 691 U/mL) at HSCT (HR 6.93), and conditioning without radiotherapy (HR 3.53) were also independently associated with poor survival. Notably, 79% of radiotherapy doses were less than 6 Gy. Regardless of the presence of hemophagocytic lymphohistiocytosis, the group with a high sIL-2R level (≥2000 U/mL) showed a poorer prognosis. Although allo-HSCT is the only curative therapy for sCAEBV, treatment strategies need to be improved for high-risk patients, especially those with high levels of sIL-2R.
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U2 - 10.1002/ajh.26544
DO - 10.1002/ajh.26544
M3 - Article
C2 - 35312194
AN - SCOPUS:85127517391
SN - 0361-8609
VL - 97
SP - 780
EP - 790
JO - American Journal of Hematology
JF - American Journal of Hematology
IS - 6
ER -