Hematopoietic stem cell transplantation in patients with severe congenital neutropenia: An analysis of 18 Japanese cases

被引:21
作者
Oshima, Koichi [1 ]
Hanada, Ryoji [1 ]
Kobayashi, Ryoji [2 ]
Kato, Koji [3 ]
Nagatoshi, Yoshihisa [4 ]
Tabuchi, Ken [5 ]
Kato, Shunichi [6 ]
机构
[1] Saitama Childrens Med Ctr, Div Hematol & Oncol, Iwatsuki Ku, Saitama 3398551, Japan
[2] Sapporo Hokuyu Hosp, Dept Pediat, Sapporo, Hokkaido, Japan
[3] Japanese Red Cross Nagoya First Hosp, Div Hematol & Oncol, Childrens Med Ctr, Nagoya, Aichi, Japan
[4] Kyushu Natl Canc Ctr, Paediat Sect, Fukuoka, Japan
[5] Kanagawa Children Med Ctr, Div Hematooncol & Regenerat Med, Yokohama, Kanagawa, Japan
[6] Tokai Univ, Sch Med, Dept Cell Transplantat & Regenerat Med, Isehara, Kanagawa 25911, Japan
关键词
severe congenital neutropenia; Kostmann syndrome; stem cell transplantation; VERSUS-HOST-DISEASE; BONE-MARROW-TRANSPLANTATION; COLONY-STIMULATING-FACTOR; PERIPHERAL-BLOOD; UNRELATED DONORS; CSF3R MUTATIONS; FOLLOW-UP; PROPHYLAXIS; CHILDREN; LEUKEMIA;
D O I
10.1111/j.1399-3046.2010.01319.x
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
We studied the outcome of allogeneic HSCT in patients with SCN. Between 1989 and 2005, 18 patients with SCN in Japan received HSCT for reasons other than malignant transformation, i.e., because of the lack of or a partial response to treatment with r-HuG-CSF. The median age of the patients at the first HSCT was three and a half yr (range 0.2-16.7 yr). Nine patients received stem cells from an HLA-identical sibling donor and nine from an alternative donor. Twelve and six patients received myeloablative and non-myeloablative conditioning regimens, respectively. Engraftment occurred at the first HSCT in 12 patients, four patients received a second HSCT for graft failure, and two patients died. The cause of death was renal failure and graft failure at the first and second HSCT, respectively. The cumulative incidence of grade II-IV acute GVHD and TRM at the first transplantation was 11% and 5.6%, respectively. Of our patients, 16 are alive and in complete remission, with a median follow-up of six and a half yr. Our results suggest that HSCT is beneficial for patients with SCN refractory to r-HuG-CSF treatment.
引用
收藏
页码:657 / 663
页数:7
相关论文
共 37 条
[1]   Nonmyeloablative stem cell transplantation for congenital immunodeficiencies [J].
Amrolia, P ;
Gaspar, HB ;
Hassan, A ;
Webb, D ;
Jones, A ;
Sturt, N ;
Mieli-Vergani, G ;
Pagliuca, A ;
Mufti, G ;
Hadzic, N ;
Davies, G ;
Veys, P .
BLOOD, 2000, 96 (04) :1239-1246
[2]   Pre-emptive treatment of acute GVHD: a randomized multicenter trial of rabbit anti-thymocyte globulin, given on day+7 after alternative donor transplants [J].
Bacigalupo, A. ;
Lamparelli, T. ;
Milone, G. ;
Sormani, M. P. ;
Ciceri, F. ;
Peccatori, J. ;
Locasciulli, A. ;
Majolino, I. ;
Di Bartolomeo, P. ;
Mazza, F. ;
Sacchi, N. ;
Pollicheni, S. ;
Pinto, V. ;
Van Lint, M. T. .
BONE MARROW TRANSPLANTATION, 2010, 45 (02) :385-391
[3]   Antithymocyte globulin for graft-versus-host disease prophylaxis in transplants from unrelated donors: 2 randomized studies from Gruppo Italiano Trapianti Midollo Osseo (GITMO) [J].
Bacigalupo, A ;
Lamparelli, T ;
Bruzzi, P ;
Guidi, S ;
Alessandrino, PE ;
di Bartolomeo, P ;
Oneto, R ;
Bruno, B ;
Barbanti, M ;
Sacchi, N ;
Van Lint, MT ;
Bosi, A .
BLOOD, 2001, 98 (10) :2942-2947
[4]   Mutations in the ELA2 gene correlate with more severe expression of neutropenia:: a study of 81 patients from the French Neutropenia Register [J].
Bellanné-Chantelot, C ;
Clauin, S ;
Leblanc, T ;
Cassinat, B ;
Rodrigues-Lima, F ;
Beaufils, S ;
Vaury, C ;
Barkaoui, M ;
Fenneteau, O ;
Maier-Redelsperger, M ;
Chomienne, C ;
Donadieu, J .
BLOOD, 2004, 103 (11) :4119-4125
[5]   EFFECTS OF RECOMBINANT HUMAN GRANULOCYTE COLONY-STIMULATING FACTOR ON NEUTROPENIA IN PATIENTS WITH CONGENITAL AGRANULOCYTOSIS [J].
BONILLA, MA ;
GILLIO, AP ;
RUGGEIRO, M ;
KERNAN, NA ;
BROCHSTEIN, JA ;
ABBOUD, M ;
FUMAGALLI, L ;
VINCENT, M ;
GABRILOVE, JL ;
WELTE, K ;
SOUZA, LM ;
OREILLY, RJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1989, 320 (24) :1574-1580
[6]   Mutations in the gene encoding neutrophil elastase in congenital and cyclic neutropenia [J].
Dale, DC ;
Person, RE ;
Bolyard, AA ;
Aprikyan, AG ;
Bos, C ;
Bonilla, MA ;
Boxer, LA ;
Kannourakis, G ;
Zeidler, C ;
Welte, K ;
Benson, KF ;
Horwitz, M .
BLOOD, 2000, 96 (07) :2317-2322
[7]   Severe chronic neutropenia: Treatment and follow-up of patients in the severe chronic neutropenia international registry [J].
Dale, DC ;
Cottle, TE ;
Fier, CJ ;
Bolyard, AA ;
Bonilla, MA ;
Boxer, LA ;
Cham, B ;
Freedman, MH ;
Kannourakis, G ;
Kinsey, SE ;
Davis, R ;
Scarlata, D ;
Schwinzer, B ;
Zeidler, C ;
Welte, K .
AMERICAN JOURNAL OF HEMATOLOGY, 2003, 72 (02) :82-93
[8]   MUTATIONS IN THE GENE FOR THE GRANULOCYTE COLONY-STIMULATING-FACTOR RECEPTOR IN PATIENTS WITH ACUTE MYELOID-LEUKEMIA PRECEDED BY SEVERE CONGENITAL NEUTROPENIA [J].
DONG, F ;
BRYNES, RK ;
TIDOW, N ;
WELTE, K ;
LOWENBERG, B ;
TOUW, IP .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 333 (08) :487-493
[9]   Peripheral blood grafts from unrelated donors are associated with increased acute and chronic graft-versus-host disease without improved survival [J].
Eapen, Mary ;
Logan, Brent R. ;
Confer, Dennis L. ;
Haagenson, Michael ;
Wagner, John E. ;
Weisdorf, Daniel J. ;
Wingard, John R. ;
Rowley, Scott D. ;
Stroncek, David ;
Gee, Adrian P. ;
Horowitz, Mary M. ;
Anasetti, Claudio .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2007, 13 (12) :1461-1468
[10]   Hematopoetic Stem Cell Transplantation in Neutrophil Disorders: Severe Congenital Neutropenia, Leukocyte Adhesion Deficiency and Chronic Granulomatous Disease [J].
Elhasid, Ronit ;
Rowe, Jacob M. .
CLINICAL REVIEWS IN ALLERGY & IMMUNOLOGY, 2010, 38 (01) :61-67