Bone marrow transplantation for paroxysmal nocturnal haemoglobinuria

被引:26
作者
Bemba, M
Guardiola, P
Garderet, L
Devergie, A
Ribaud, P
Esperou, H
Noguera, MH
Gluckman, E
Socié, G
机构
[1] Hop St Louis, Serv Greffe Moelle, F-75475 Paris 10, France
[2] Hop St Louis, Cent Hematol Lab, F-75475 Paris, France
关键词
paroxysmal nocturnal haemoglobinuria; bone marrow transplantation; long-term follow-up;
D O I
10.1046/j.1365-2141.1999.01374.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Paroxysmal nocturnal haemoglobinuria (PNH) is an acquired clonal disorder of the haemopoietic stem cells for which the only curative treatment is bone marrow transplantation. There are few reports on the use of allogeneic transplantation for PNH, and nearly all of them include only a few patients. Between September 1978 and December 1997, 16 patients underwent marrow transplantation for PNH at the Hospital Saint Louis. The 5-year survival rate for the 16 patients was 58 +/- 13%, Two factors, an absolute neutrophil count >1.0 x 10(9)/l and haemoglobin level >9 g/dl at transplant, were found to be statistically associated with a better outcome.
引用
收藏
页码:366 / 368
页数:3
相关论文
共 9 条
[1]  
ANTIN JH, 1985, BLOOD, V66, P1247
[2]   Syngeneic bone marrow transplantation without conditioning in a patient with paroxysmal nocturnal hemoglobinuria: In vivo evidence that the mutant stem cells have a survival advantage [J].
Endo, M ;
Beatty, PG ;
Vreeke, TM ;
Wittwer, CT ;
Singh, SP ;
Parker, CJ .
BLOOD, 1996, 88 (02) :742-750
[3]   Resolution of Budd-Chiari syndrome following bone marrow transplantation for paroxysmal nocturnal haemoglobinuria [J].
Graham, ML ;
Rosse, WF ;
Halperin, EC ;
Miller, CR ;
Ware, RE .
BRITISH JOURNAL OF HAEMATOLOGY, 1996, 92 (03) :707-710
[4]   APLASTIC-ANEMIA AND PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA - SEARCH FOR A PATHOGENETIC LINK [J].
GRISCELLIBENNACEUR, A ;
GLUCKMAN, E ;
SCROBOHACI, ML ;
JONVEAUX, P ;
VU, T ;
BAZARBACHI, A ;
CAROSELLA, ED ;
SIGAUX, F ;
SOCIE, G .
BLOOD, 1995, 85 (05) :1354-1363
[5]   MARROW TRANSPLANTATION FOR PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA [J].
KAWAHARA, K ;
WITHERSPOON, RP ;
STORB, R .
AMERICAN JOURNAL OF HEMATOLOGY, 1992, 39 (04) :283-288
[6]   Somatic mutations in paroxysmal nocturnal hemoglobinuria: A blessing in disguise? [J].
Luzzatto, L ;
Bessler, M ;
Rotoli, B .
CELL, 1997, 88 (01) :1-4
[7]   Bone marrow transplants for paroxysmal nocturnal haemoglobinuria [J].
Saso, R ;
Marsh, J ;
Cevreska, L ;
Szer, J ;
Gale, RP ;
Rowlings, PA ;
Passweg, JR ;
Nugent, ML ;
Luzzatto, L ;
Horowitz, MM ;
Gordon-Smith, EC .
BRITISH JOURNAL OF HAEMATOLOGY, 1999, 104 (02) :392-396
[8]   Paroxysmal nocturnal haemoglobinuria: Long-term follow-up and prognostic factors [J].
Socie, G ;
Mary, JY ;
deGramont, A ;
Rio, B ;
Leporrier, M ;
Rose, C ;
Heudier, P ;
Rochant, H ;
Cahn, JY ;
Gluckman, E .
LANCET, 1996, 348 (9027) :573-577
[9]   Recent advances in paroxysmal nocturnal hemoglobinuria. From the biology to the clinic [J].
Socie, G .
HEMATOLOGY AND CELL THERAPY, 1997, 39 (04) :175-187