Hematopoietic stem cell transplantation for children with high-risk acute lymphoblastic leukemia in first complete remission: a report from the AIEOP registry

被引:23
作者
Fagioli, Franca [1 ]
Quarello, Paola [1 ]
Zecca, Marco [2 ]
Lanino, Edoardo [3 ]
Rognoni, Carla [4 ,5 ]
Balduzzi, Adriana [6 ]
Messina, Chiara [7 ]
Favre, Claudio [8 ]
Foa, Roberto [9 ]
Ripaldi, Mimmo [10 ]
Rutella, Sergio [11 ]
Basso, Giuseppe [12 ]
Prete, Arcangelo [13 ]
Locatelli, Franco [11 ,14 ]
机构
[1] Regina Margherita Childrens Hosp, Pediat Oncohematol Stem Cell Transplantat & Cellu, Turin, Italy
[2] Policlin San Matteo Fdn, IRCCS, Dept Pediat Oncohematol, Pavia, Italy
[3] G Gaslini Inst Children, Dept Pediat Hematol Oncol, Genoa, Italy
[4] Univ Pavia, Dept Ind & Informat Engn, I-27100 Pavia, Italy
[5] Bocconi Univ, Ctr Res Hlth & Social Care Management CERGAS, Milan, Italy
[6] San Gerardo Hosp, Dept Pediat Hematol, Monza, Italy
[7] Univ Padua, Dept Pediat Hematol & Oncol, Padua, Italy
[8] Univ Pisa, Dept Pediat, Pisa, Italy
[9] Univ Roma La Sapienza, Dept Cellular Biotechnol & Hematol, Div Hematol, I-00185 Rome, Italy
[10] Santobono Pausilipon Hosp, Dept Pediat Hematooncol, BMT Unit, Naples, Italy
[11] Bambino Gesu Pediat Hosp, Dept Pediat Hematol Oncol, IRCCS, Rome, Italy
[12] Univ Padua, Dept Pediat, Lab Hematol Oncol, Padua, Italy
[13] Univ Bologna, St Orsola Malpighi Hosp, Dept Pediat, Pediat Oncol & Hematol Unit Lalla Seragnoli, Bologna, Italy
[14] Univ Pavia, I-27100 Pavia, Italy
关键词
MINIMAL-RESIDUAL-DISEASE; BONE-MARROW-TRANSPLANTATION; TIME QUANTITATIVE PCR; T-CELL; ALLOGENEIC TRANSPLANTATION; CONDITIONING REGIMENS; BLOOD TRANSPLANTATION; GENE REARRANGEMENTS; CHILDHOOD; CHEMOTHERAPY;
D O I
10.3324/haematol.2012.079707
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Children with high-risk acute lymphoblastic leukemia in first complete remission can benefit from allogeneic hematopoietic stem cell transplantation. We analyzed the outcome of 211 children with high-risk acute lymphoblastic leukemia in first complete remission who were given an allogeneic transplant between 1990 and 2008; the outcome of patients who, despite having an indication for transplantation and a suitable donor, did not receive the allograft for different reasons in the same time period was not analyzed. Sixty-nine patients (33%) were transplanted between 1990 and 1999, 58 (27%) between 2000 and 2005, and 84 (40%) between 2005 and 2008. A matched family donor was employed in 138 patients (65%) and an unrelated donor in 73 (35%). The 10-year probabilities of overall and disease-free survival were 63.4% and 61%, respectively. The 10-year cumulative incidences of transplantation-related mortality and relapse were 15% and 24%, respectively. After 1999, no differences in either disease-free survival or transplant-related mortality were observed in patients transplanted from unrelated or matched family donors. In multivariate analysis, grade IV acute graft-versus-host disease was an independent factor associated with worse disease-free survival. By contrast, grade I acute graft-versus-host disease and age at diagnosis between 1 and 9 years were favorable prognostic variables. Our study, not intended to evaluate whether transplantation is superior to chemotherapy for children with acute lymphoblastic leukemia in first complete remission and high-risk features, shows that the allograft cured more than 60% of these patients; in the most recent period, the outcome of recipients of grafts from matched family and unrelated donors was comparable.
引用
收藏
页码:1273 / 1281
页数:9
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