Treatment choice of immunotherapy or further chemotherapy for Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis

被引:25
|
作者
Shiraishi, Akira [2 ]
Ohga, Shouichi [1 ,2 ]
Doi, Takehiko [2 ]
Ishimura, Masataka [2 ]
Takimoto, Tomohito [2 ]
Takada, Hidetoshi [2 ]
Miyamoto, Toshihiro [3 ]
Abe, Yasunobu [4 ]
Hara, Toshiro [2 ]
机构
[1] Kyushu Univ, Grad Sch Med Sci, Dept Perinatal & Pediat Med, Higashi Ku, Fukuoka 8128582, Japan
[2] Kyushu Univ, Dept Pediat, Grad Sch Med Sci, Fukuoka 8128582, Japan
[3] Kyushu Univ, Grad Sch Med Sci, Dept Med & Biosyst Sci, Fukuoka 8128582, Japan
[4] Kyushu Univ, Grad Sch Med Sci, Dept Med & Bioregulatory Sci, Fukuoka 8128582, Japan
关键词
Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis; etoposide; familial hemophagocytic lymphohistiocytosis; hematopoietic stem cell transplantation; immunochemotherapy; STEM-CELL TRANSPLANTATION; ACTIVE EBV INFECTION; T-CELLS; LYMPHOPROLIFERATIVE DISEASE; ADULT PATIENTS; CLINICAL-SIGNIFICANCE; INTERFERON-GAMMA; JAPAN; IMMUNOCHEMOTHERAPY; MONONUCLEOSIS;
D O I
10.1002/pbc.24039
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background EpsteinBarr virus-associated hemophagocytic lymphohistiocytosis (EBV-HLH) leads to an aggressive and often fatal course without appropriate treatment. Etoposide therapy is crucial for the better prognosis, although it remains unknown what patients need cytotoxic agents. Since we have complied with step-up strategy in a tertiary center, treatment outcomes were studied to search predictors for disease course. Methods The study enrolled 22 EBV-HLH patients treated between 1999 and 2010 in Kyushu University. Immunotherapy, chemotherapy and stem cell transplantation (SCT) proceeded in stages unless patients attained a consecutive >21 days-afebrile remission. Clinical and laboratory data and outcomes were retrospectively analyzed. Results Median age of 9 males and 13 females was 5 years (range: 9 months41 years). Sixteen patients (73%) presented at age <15 years. Two patients remitted spontaneously, 12 attained remissions after immunotherapy, 5 after chemotherapy, and 1 after successful SCT. The remaining two patients died after chemotherapy and SCT, respectively. Median EBV load was 1 x 105?copies/ml of peripheral blood (range: 2005 x 107). T-cells were exclusively targeted (94%; 15/16 examined) often with EBV/T-cell receptor clonality. EBV status indicated 19 primary infections and 3 reactivations. Either death occurred in EBV-reactivated patients who underwent chemotherapy +/- SCT. Age at primary infection in pediatric patients increased in the last 5 years. Patients having prolonged fever (P?=?0.017) or high soluble CD25 levels (P?=?0.017) at diagnosis were at higher risk for requiring chemotherapy assessed by multivariate analyses. Conclusions No cytotoxic agents were needed for >60% of EBV-HLH patients. Early immunotherapy may modulate T-cell activation and reduce the chance of unnecessary chemotherapy. Pediatr Blood Cancer 2012;59:265270. (c) 2011 Wiley Periodicals, Inc.
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收藏
页码:265 / 270
页数:6
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