T-cell receptor excision circles: a novel prognostic parameter for the outcome of transplantation in multiple myeloma patients

被引:23
作者
Svaldi, M
Lanthaler, AJ
Dugas, M
Lohse, P
Pescosta, N
Straka, C
Mitterer, M
机构
[1] Reg Hosp Bozen, Dept Hematol, I-39100 Bolzano, Italy
[2] Reg Hosp Bozen, Bone Marrow Transplantat Ctr, I-39100 Bolzano, Italy
[3] Univ Munich, Dept Clin Chem Grosshadern, Munich, Germany
[4] Univ Munich, Dept Med Informat Biometr & Epidemiol, Munich, Germany
[5] Univ Munich, Med Klin Innenstadt, D-8000 Munich, Germany
关键词
multiple myeloma; autologous transplantation; survival; infections; T-cell receptor excision circles (TRECs);
D O I
10.1046/j.1365-2141.2003.04482.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This study investigated whether T-cell receptor excision circles (TRECs) are a prognostic marker for the outcome of myeloma patients undergoing a tandem autologous peripheral blood stem cell transplantation (PBSCT). Twenty-five patients were enrolled. Samples were obtained at study enrolment, after conventional therapy, between first and second transplantation and 3, 6, 12 and 24 months after the second PBSCT. TRECs were quantified using real-time polymerase chain reaction. A high variation in TREC levels was found at diagnosis (median TREC level 136/10(5) peripheral blood mononuclear cells (PBMCs); range 1-1729), suggesting individual differences in thymic output of naive T cells. Patients with more than 136 TRECs/10(5) P BMCs at diagnosis had a statistically significant better overall survival (P = 0.05) and event-free survival (P = 0.045), whereas low TREC levels correlated with a higher incidence of infectious complications. Median TREC values were lowest after the first PBSCT (52/10(5) PBMCs) and reached the baseline 12 months after the second transplantation. Patients with high TREC levels after the second PBSCT had a significantly higher probability of being in complete or partial remission 30 months after the second PBSCT. TREC levels were not correlated with beta(2)-microglobulin and C-reactive protein levels at diagnosis. These data suggest that TRECs could be a relevant prognostic factor for patients who receive high-dose chemotherapy and autologous PBSCT.
引用
收藏
页码:795 / 801
页数:7
相关论文
共 34 条
[1]   Detection of T cell receptor circles (TRECs) as biomarkers for de novo T cell synthesis using a quantitative polymerase chain reaction-enzyme linked immunosorbent assay (PCR-ELISA) [J].
Al-Harthi, L ;
Marchetti, G ;
Steffens, CM ;
Poulin, JF ;
Sékaly, RP ;
Landay, A .
JOURNAL OF IMMUNOLOGICAL METHODS, 2000, 237 (1-2) :187-197
[2]   A prospective, randomized trial of autologous bone marrow transplantation and chemotherapy in multiple myeloma [J].
Attal, M ;
Harousseau, JL ;
Stoppa, AM ;
Sotto, JJ ;
Fuzibet, JG ;
Rossi, JF ;
Casassus, P ;
Maisonneuve, H ;
Facon, T ;
Ifrah, N ;
Payen, C ;
Bataille, R .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (02) :91-97
[3]   Superiority of tandem autologous transplantation over standard therapy for previously untreated multiple myeloma [J].
Barlogie, B ;
Jagannath, S ;
Vesole, DH ;
Naucke, S ;
Cheson, B ;
Mattox, S ;
Bracy, D ;
Salmon, S ;
Jacobson, J ;
Crowley, J ;
Tricot, G .
BLOOD, 1997, 89 (03) :789-793
[4]  
BARLOGIE B, 1999, 7 INT MULT MYEL WORK, P49
[5]  
BATAILLE R, 1992, BLOOD, V80, P733
[6]   Immunologic effects of prophylactic donor lymphocyte infusion after allogeneic marrow transplantation for multiple myeloma [J].
Bellucci, R ;
Alyea, EP ;
Weller, E ;
Chillemi, A ;
Hochberg, E ;
Wu, CJ ;
Canning, C ;
Schlossman, R ;
Soiffer, RJ ;
Anderson, KC ;
Ritz, J .
BLOOD, 2002, 99 (12) :4610-4617
[7]  
Blade Joan, 1998, British Journal of Haematology, V102, P1115, DOI 10.1046/j.1365-2141.1998.00930.x
[8]   Lymphoid reconstitution after autologous PBSC transplantation with FACS-sorted CD34+ hematopoietic progenitors [J].
Bomberger, C ;
Singh-Jairam, M ;
Rodey, G ;
Guerriero, A ;
Yeager, AM ;
Fleming, WH ;
Holland, HK ;
Waller, EK .
BLOOD, 1998, 91 (07) :2588-2600
[9]   The prognostic significance of T cell receptor beta gene rearrangements and idiotype-reactive T cells in multiple myeloma [J].
Brown, RD ;
Yuen, E ;
Nelson, M ;
Gibson, J ;
Joshua, D .
LEUKEMIA, 1997, 11 (08) :1312-1317
[10]   Nonmyeloablative regimen preserves "niches" allowing for peripheral expansion of donor T-cells [J].
Chao, NJ ;
Liu, CX ;
Rooney, B ;
Chen, BJ ;
Long, GD ;
Vredenburgh, JJ ;
Morris, A ;
Gasparetto, C ;
Rizzieri, DA .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2002, 8 (05) :249-256