Prognostic value of soluble interleukin 2 receptor levels in Langerhans cell histiocytosis

被引:33
作者
Rosso, DA
Roy, A
Zelazko, M
Braier, JL
机构
[1] Hosp Pediat SAMIC Prof Dr Juan P Garrahan, Dept Hematol Oncol, Buenos Aires, DF, Argentina
[2] Hosp Pediat SAMIC Prof Dr Juan P Garrahan, Dept Immunol, Buenos Aires, DF, Argentina
关键词
Langerhans cell histiocytosis; soluble interleukin 2 receptor; prognosis; childhood; infant;
D O I
10.1046/j.1365-2141.2002.03400.x
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
We investigated the prognostic significance of soluble interleukin 2 receptor (sIL-2r) levels in the pre- and post-treatment serum of paediatric patients with Langerhans cell histiocytosis (LCH). Serum levels of sIL-2r from 32 LCH patients and 14 healthy controls were determined using enzyme-linked immunosorbent assay. The LCH patients were classified, evaluated and treated according to the Histiocyte Society's protocols. The following clinical stages were considered: single-system disease (A) divided into single-site (A1; n=4), multiple-site (A2; n=9), and multisystem disease (B) without organ dysfunction (B1; n=5) and with organ dysfunction (B2; n=14). Pretreatment concentrations of sIL-2r were markedly increased at diagnosis in LCH patients compared with controls [in pg/ml, median (range) 9200 (1124-40000) versus 610 (343-800)], P <0.0001. Levels differed significantly between stages A [3250 (1124-11000)] and B [22750 (3400-40000)], P<0.05, and between substages A2 and B2, P <0.05. There was a significant correlation between clinical stages and sIL-2r serum levels, r=0.7996 (P <0.0001). Patients with greater than or equal to17500 pg/ml of sIL-2r had a 30-month survival of 0.417 (SEM: 0.142) compared with those with levels <17500 pg/ml, who presented a 30-month survival of 0.848 (SEM: 0.100) (log-rank, P <0.0001). In multivariate analysis, sIL-2r levels greater than or equal to17500 pg/ml were found to have greater predictive strength than other well-known prognostic factors.
引用
收藏
页码:54 / 58
页数:5
相关论文
共 12 条
[1]
BARBEY S, 1987, Pediatric Pathology, V7, P569
[2]
Langerhans cell histiocytosis: Retrospective evaluation of 123 patients at a single institution [J].
Braier, J ;
Chantada, G ;
Rosso, D ;
Bernaldez, P ;
Amaral, D ;
Latella, A ;
Balancini, B ;
Masautis, A ;
Goldberg, J .
PEDIATRIC HEMATOLOGY AND ONCOLOGY, 1999, 16 (05) :377-385
[3]
Current therapy for Langerhans cell histiocytosis [J].
Broadbent, V ;
Gadner, H .
HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA, 1998, 12 (02) :327-+
[4]
Egeler RM, 1999, BLOOD, V94, P4195
[5]
Soluble cytokine receptors: Their roles in immunoregulation, disease, and therapy [J].
FernandezBotran, R ;
Chilton, PM ;
Ma, YH .
ADVANCES IN IMMUNOLOGY, VOL 63, 1996, 63 :269-336
[6]
Karnitz LM, 1996, ADV IMMUNOL, V61, P147, DOI 10.1016/S0065-2776(08)60867-6
[7]
KOMP DM, 1989, BLOOD, V73, P2128
[8]
The epidemiology of Langerhans cell histiocytosis [J].
Nicholson, HS ;
Egeler, RM ;
Nesbit, ME .
HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA, 1998, 12 (02) :379-+
[9]
Nosology and pathology of Langerhans cell histiocytosis [J].
Schmitz, L ;
Favara, BE .
HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA, 1998, 12 (02) :221-+
[10]
Schultz C, 1998, MED PEDIATR ONCOL, V31, P61, DOI 10.1002/(SICI)1096-911X(199808)31:2<61::AID-MPO3>3.0.CO