Impact of pretransplant minimal residual disease after cord blood transplantation for childhood acute lymphoblastic leukemia in remission: an Eurocord, PDWP–EBMT analysis

被引:0
作者
A Ruggeri
G Michel
J-H Dalle
M Caniglia
F Locatelli
A Campos
C D de Heredia
M Mohty
J M P Hurtado
M Bierings
H Bittencourt
M Mauad
D Purtill
R Cunha
N Kabbara
E Gluckman
M Labopin
C Peters
V Rocha
机构
[1] Eurocord,Dipartimento di Oncoematologia Pediatrica
[2] Hôpital Saint Louis APHP,Department Hematologie
[3] University Paris VII IUH,Department of Hematology
[4] Rome Transplant Network,undefined
[5] University Tor Vergata,undefined
[6] Hôpital d'Enfants de la Timone,undefined
[7] Service d’Hématologie,undefined
[8] Hôpital Robert Debré,undefined
[9] APHP,undefined
[10] Ospedale Bambino Gesù,undefined
[11] IRCSS,undefined
[12] Università di Pavia,undefined
[13] Roma,undefined
[14] BMT Unit,undefined
[15] Institute Portugues Oncologia,undefined
[16] Servicio de Hematologia y Oncologia Pediátrica,undefined
[17] Hospital Vall d'Hebron,undefined
[18] Hotel Dieu,undefined
[19] Unidad de Hematología Pediátrica,undefined
[20] Hospital Virgen del Rocio,undefined
[21] University Hospital for Children,undefined
[22] Centre de Cancérologie Charles-Bruneau,undefined
[23] Ste-Justine Hospital,undefined
[24] Til,undefined
[25] Acute Leukemia Working Party,undefined
[26] EBMT,undefined
[27] Hopital Saint Antoine,undefined
[28] Paediatric Diseases Working Party,undefined
[29] EBMT,undefined
[30] BMT Unit,undefined
[31] St. Anna Kinderspital,undefined
[32] Sirio Libanes Hospital and Cancer Children’s Hospital (ITACI),undefined
[33] University of Sao Paulo,undefined
来源
Leukemia | 2012年 / 26卷
关键词
cord blood transplantation; children; minimal residual disease; relapse; acute lymphoblastic leukemia;
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学科分类号
摘要
To address the prognostic value of minimal residual disease (MRD) before unrelated cord blood transplantation (UCBT) in children with acute lymphoblastic leukemia (ALL), we analyzed 170 ALL children transplanted in complete remission (CR) after myeloablative conditioning regimen. In all, 72 (43%) were in first CR (CR1), 77 (45%) in second CR (CR2) and 21 (12%) in third CR (CR3). The median interval from MRD quantification to UCBT was 18 days. All patients received single-unit UCBT. Median follow-up was 4 years. Cumulative incidence (CI) of day-60 neutrophil engraftment was 85%. CI of 4 years relapse was 30%, incidence being lower in patients with negative MRD before UCBT (hazard ratio (HR)=0.4, P=0.01) and for those transplanted in CR1 and CR2 (HR=0.3, P=0.002). Probability of 4 years leukemia-free survival (LFS) was 44%, (56, 44 and 14% for patients transplanted in CR1, CR2 and CR3, respectively (P=0.0001)). Patients with negative MRD before UCBT had better LFS after UCBT compared with those with positive MRD (54% vs 29%; HR=2, P=0.003). MRD assessment before UCBT for children with ALL in remission allows identifying patients at higher risk of relapse after transplantation. Approaches that may decrease relapse incidence in children given UCBT with positive MRD should be investigated to improve final outcomes.
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页码:2455 / 2461
页数:6
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