Analysis of Risk Factors for Outcomes After Unrelated Cord Blood Transplantation in Adults With Lymphoid Malignancies: A Study by the Eurocord-Netcord and Lymphoma Working Party of the European Group for Blood and Marrow Transplantation

被引:142
作者
Rodrigues, Celso A. [1 ]
Sanz, Guillermo
Brunstein, Claudio G.
Sanz, Jaime
Wagner, John E.
Renaud, Marc
de Lima, Marcos
Cairo, Mitchell S.
Fuerst, Sabine
Rio, Bernard
Dalley, Christopher
Carreras, Enric
Harousseau, Jean-Luc
Mohty, Mohamad
Taveira, Denis
Dreger, Peter
Sureda, Anna
Gluckman, Eliane
Rocha, Vanderson
机构
[1] Hop St Louis, Eurocord ARTM, Eurocord Off, F-75475 Paris 10, France
关键词
STEM-CELL TRANSPLANTATION; CHRONIC LYMPHOCYTIC-LEUKEMIA; ALLOGENEIC HEMATOPOIETIC TRANSPLANTATION; NON-HODGKINS-LYMPHOMA; BONE-MARROW; AUTOLOGOUS TRANSPLANTATION; SOCIETY; RELAPSE; CHEMOTHERAPY; FLUDARABINE;
D O I
10.1200/JCO.2007.15.8865
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose To determine risk factors of umbilical cord blood transplantation (UCBT) for patients with lymphoid malignancies. Patients and Methods We evaluated 104 adult patients (median age, 41 years) who underwent unrelated donor UCBT for lymphoid malignancies. UCB grafts were two-antigen human leukocyte antigen-mismatched in 68%, and were composed of one (n = 78) or two (n = 26) units. Diagnoses were non-Hodgkin's lymphoma (NHL, n = 61), Hodgkin's lymphoma (HL, n = 29), and chronic lymphocytic leukemia (CLL, n = 14), with 87% having advanced disease and 60% having experienced failure with a prior autologous transplant. Sixty-four percent of patients received a reduced-intensity conditioning regimen and 46% low-dose total-body irradiation (TBI). Median follow-up was 18 months. Results Cumulative incidence of neutrophil engraftment was 84% by day 60, with greater engraftment in recipients of higher CD34(+) kg/cell dose (P = .0004). CI of non-relapse-related mortality (NRM) was 28% at 1 year, with a lower risk in patients treated with low-dose total-body irradiation (TBI; P = .03). Cumulative incidence of relapse or progression was 31% at 1 year, with a lower risk in recipients of double-unit UCBT (P = .03). The probability of progression-free survival (PFS) was 40% at 1 year, with improved survival in those with chemosensitive disease (49% v 34%; P = .03), who received conditioning regimens containing low-dose TBI (60% v 23%; P = .001), and higher nucleated cell dose (49% v 21%; P = .009). Conclusion UCBT is a viable treatment for adults with advanced lymphoid malignancies. Chemosensitive disease, use of low-dose TBI, and higher cell dose were factors associated with significantly better outcome.
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收藏
页码:256 / 263
页数:8
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