Do corticosteroids add any benefit to standard GVHD prophylaxis in allogeneic BMT?

被引:6
作者
Ancín, I
Ferrá, C
Gallardo, D
Peris, J
Berlanga, J
Gonzalez, JR
Virgili, N
Grañena, A
机构
[1] Hosp Duran & Reynals, Inst Catala Oncol, Dept Clin Hematol, Barcelona 08907, Spain
[2] Hosp Duran & Reynals, Canc Prevent & Control Unit, Barcelona, Spain
[3] Hosp Principes Espana, Dept Endocrinol, Barcelona, Spain
关键词
allogeneic bone marrow transplantation; acute graft-versus-host disease prophylaxis; corticosteroids;
D O I
10.1038/sj.bmt.1703085
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
In a retrospective study, we compared 15 patients who received cyclosporine (CsA), methotrexate (MTX) and prednisone (PDN) and 15 patients who received CsA-MTX for GVHD prophylaxis after allogeneic BMT (HLA-identical sibling (n = 22), related one HLA mismatch (n = 1), unrelated matched donors (n = 6), unrelated one HLA mismatch (n = 1)). The primary objectives of this study were to compare the incidence of GVHD and post-transplantation complications. Secondary objectives were to compare relapse rate, transplant-related mortality and overall survival. The incidence of acute GVHD grade III-IV was similar between the two groups (P = 0.66), as was the incidence of chronic GVHD (P = 0.67). Incidence of arterial hypertension was significantly higher in patients who received prophylactic PDN, (P = 0.03) and more insulin treatment was required in this group (P = 0.003). We observed no differences in the incidence of infections or upper digestive tract bleeding. Musculoskeletal complications appeared earlier in the group which received PDN. With a median follow-up of 4.4 years, patients in the CsA-MTX group had better overall survival, 46.7% vs 13.3% (P = 0.026). Relapse was a more frequent cause of death in the CsA-MTX group, whereas procedure-related mortality was more frequent in the CsA-MTX-PDN group (P = 0.013). These results suggest that prophylactic prednisone when combined with cyclosporine and methotrexate adds no benefit in acute or chronic GVHD prevention and may increase the morbidity of allogeneic transplantation. Corticosteroids may be reserved for GVHD treatment.
引用
收藏
页码:39 / 45
页数:7
相关论文
共 47 条
[1]  
ASCHAN J, 1991, BONE MARROW TRANSPL, V7, P113
[2]   IMPAIRMENT OF LEUKEMIA-FREE SURVIVAL BY ADDITION OF INTERLEUKIN-2-RECEPTOR ANTIBODY TO STANDARD GRAFT-VERSUS-HOST PROPHYLAXIS [J].
BLAISE, D ;
OLIVE, D ;
MICHALLET, M ;
MARIT, G ;
LEBLOND, V ;
MARANINCHI, D .
LANCET, 1995, 345 (8958) :1144-1146
[3]  
BORTIN MM, 1981, TRANSPLANT P, V13, P227
[4]  
BUTTURINI A, 1988, BONE MARROW TRANSPL, V3, P245
[5]   Low dose T-cell lymphocyte infusion combined with marrow T-cell depletion as prophylaxis of acute graft vs host disease for HLA identical sibling bone marrow transplantation [J].
Cahn, JY ;
Deconinck, E ;
Tiberghien, P ;
Brion, A ;
Racadot, E ;
Deschaseaux, M ;
Angonin, R ;
Voillat, L ;
Vuillier, J ;
Fontan, J ;
Morel, P ;
Cordonnier, JM ;
Comparot, S ;
Woronoff-Lemsi, MC ;
Hervé, P .
HEMATOLOGY AND CELL THERAPY, 1999, 41 (02) :31-37
[6]   Low-dose cyclosporine of short duration increases the risk of mild and moderate GVHD and reduces the risk of relapse in HLA-identical sibling marrow transplant recipients with leukaemia [J].
Carlens, S ;
Aschan, J ;
Remberger, M ;
Dilber, MS ;
Ringdén, O .
BONE MARROW TRANSPLANTATION, 1999, 24 (06) :629-635
[7]  
Champlin R, 1993, J Hematother, V2, P27, DOI 10.1089/scd.1.1993.2.27
[8]   CYCLOSPORINE, METHOTREXATE, AND PREDNISONE COMPARED WITH CYCLOSPORINE AND PREDNISONE FOR PROPHYLAXIS OF ACUTE GRAFT-VERSUS-HOST DISEASE [J].
CHAO, NJ ;
SCHMIDT, GM ;
NILAND, JC ;
AMYLON, MD ;
DAGIS, AC ;
LONG, GD ;
NADEMANEE, AP ;
NEGRIN, RS ;
ODONNELL, MR ;
PARKER, PM ;
SMITH, EP ;
SNYDER, DS ;
STEIN, AS ;
WONG, RM ;
BLUME, KG ;
FORMAN, SJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1993, 329 (17) :1225-1230
[9]  
COX DR, 1972, J R STAT SOC B, V34, P187
[10]   CYCLOSPORINE AS PROPHYLAXIS FOR GRAFT-VERSUS-HOST DISEASE - A RANDOMIZED STUDY IN PATIENTS UNDERGOING MARROW TRANSPLANTATION FOR ACUTE NONLYMPHOBLASTIC LEUKEMIA [J].
DEEG, HJ ;
STORB, R ;
THOMAS, ED ;
FLOURNOY, N ;
KENNEDY, MS ;
BANAJI, M ;
APPELBAUM, FR ;
BENSINGER, WI ;
BUCKNER, CD ;
CLIFT, RA ;
DONEY, K ;
FEFER, A ;
MCGUFFIN, R ;
SANDERS, JE ;
SINGER, J ;
STEWART, P ;
SULLIVAN, KM ;
WITHERSPOON, RP .
BLOOD, 1985, 65 (06) :1325-1334