Registry data analysis of hematopoietic stem cell transplantation on systemic chronic active Epstein–Barr virus infection patients in Japan

医学 危险系数 造血干细胞移植 内科学 噬血细胞性淋巴组织细胞增多症 比例危险模型 移植 置信区间 年轻人 胃肠病学 病毒载量 免疫学 疾病 病毒
作者
Masahide Yamamoto,Maho Sato,Yasushi Onishi,Yoji Sasahara,Hideki Sano,Masayoshi Masuko,Hirohisa Nakamae,Ken‐ichi Matsuoka,Takahide Ara,Kana Washio,Makoto Onizuka,Kenichiro Watanabe,Yoshiyuki Takahashi,Tsuneaki Hirakawa,Miwako Nishio,Chizuko Sakashita,Tohru Kobayashi,Akihisa Sawada,Tatsuo Ichinohe,Takahiro Fukuda
出处
期刊:American Journal of Hematology [Wiley]
卷期号:97 (6): 780-790 被引量:10
标识
DOI:10.1002/ajh.26544
摘要

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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