Matched unrelated donor transplantation versus haploidentical transplantation with post-transplant cyclophosphamide in children with acute myeloid leukemia: a PDWP-EBMT study

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作者
Ruggeri, Annalisa [1 ]
Santoro, Nicole [2 ]
Galimard, Jacques -Emmanuel [3 ]
Kalwak, Krzysztof [4 ]
Algeri, Mattia [5 ,6 ]
Zubarovskaya, Ludmila [7 ]
Czyzewski, Krzysztof [8 ]
Skorobogatova, Elena [9 ]
Sedlacek, Petr [10 ]
Besley, Caroline [1 ,11 ]
Balduzzi, Adriana [12 ,13 ]
Bertrand, Yves [14 ]
Peristeri, Julia [15 ]
Fagioli, Franca [16 ]
Ifversen, Mariane [17 ]
Gozdzik, Jolanta [18 ]
Peters, Christina [19 ]
Versluijs, Birgitta [20 ]
Biffi, Alessandra [21 ]
Prete, Arcangelo [22 ]
Faraci, Maura [23 ]
Ghemlas, Ibrahim [24 ]
Bodova, Ivana [25 ]
Aleinikova, Olga [26 ]
Dalissier, Arnaud [27 ]
Rocha, Vanderson [28 ]
Corbacioglu, Selim [29 ]
机构
[1] IRCCS San Raffaele Sci Inst, Milan, Italy
[2] St Spirito Hosp, Dept Oncol & Hematol, Hematol Unit, Pescara, Italy
[3] EBMT Stat Unit, Paris, France
[4] Wroclaw Med Univ, Dept Pediat Hematol Oncol & Bone Marrow Transplant, Wroclaw, Poland
[5] IRCCS Bambino Gesu Childrens Hosp, Dept Pediat Hematol Oncol, Rome, Italy
[6] Magna Graecia Univ Catanzaro, Dept Hlth Sci, Catanzaro, Italy
[7] Pavlov Univ, RM Gorbacheva Res Inst, St Petersburg, Russia
[8] Nicolaus Copernicus Univ Torun, Dept Pediat Hematol & Oncol, Coll Medicum, Bydgoszcz, Poland
[9] Russian Childrens Res Hosp, Dept Bone Marrow Transplantat, Moscow, Russia
[10] Univ Hosp Motol, Dept Pediat Hematol & Oncol, Prague, Czech Republic
[11] Bristol Royal Hosp Children, Dept Pediat Oncol BMT, Bristol, England
[12] Fdn IRCCS San Gerardo Tintori, Hematopoiet Stem Cell Transplantat Unit, Monza, Italy
[13] Milano Bicocca Univ, Dept Med & Surg, Monza, Italy
[14] Inst Hematol & Oncol Pediat, Lyon, France
[15] St Sophia Childrens Hosp, Oncol Ctr, Athens, Greece
[16] Onco Ematol Pediat Ctr Trapianti Cellule Staminali, Turin, Italy
[17] Copenhagen Univ Hosp, Rigshosp, Dept Children & Adolescents Med, Copenhagen, Denmark
[18] Jagiellonian Univ Med Coll, Childrens Hosp Krakow, Dept Clin Immunol & Transplantat, Krakow, Poland
[19] Med Univ Vienna, St Anna Childrens Hosp, Dept Pediat, Vienna, Austria
[20] Princess Maxima Ctr, Utrecht, Netherlands
[21] Clin Oncoematol Pediat, Dipartimento Pediat, Padua, Italy
[22] IRCCS Azienda Osped Univ, Bologna, Italy
[23] IRCSS Ist G Gaslini, Dept Hemato Oncol, HSCT Unit, Genoa, Italy
[24] King Faisal Specialist Hosp & Res Ctr, Pediat Hematol Oncol, Riyadh, Saudi Arabia
[25] Pediat Univ, Childrens Clin Bratislava 2, Teaching Hosp, BMT Unit, Bratislava, Slovakia
[26] Belorussian Ctr Pediat Oncol & Hematol, Minsk, BELARUS
[27] 27 EBMT Paris Study Unit, Paris, France
[28] Sao Paolo Univ, BMT Unit, Sao Paulo, Brazil
[29] 29 Univ Regensburg, Regensburg, Germany
来源
关键词
STEM-CELL TRANSPLANTATION; BONE-MARROW-TRANSPLANTATION; ACUTE LYMPHOBLASTIC-LEUKEMIA; HEMATOLOGIC MALIGNANCIES; T-CELL; SIBLING DONORS; RISK; DIAGNOSIS; CRITERIA; RELAPSE;
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摘要
In children with acute myeloid leukemia (AML) who lack a human leukocyte antigen (HLA) identical sibling, the donor can be replaced with an HLA-matched unrelated donor (MUD) or a haploidentical donor (haplo). We compared outcomes of patients <18 years with AML in first and second complete remission (CR1 & CR2) undergoing a hematopoietic stem cell transplantation (HCT) either with a MUD with anti-thymocyte globulin (ATG) (N=420) or a haplo HCT with post -transplant cyclophosphamide (PT-CY) (N=96) after a myeloablative conditioning regimen (MAC) between 2011 and 2021, reported to the European Society for Blood and Marrow Transplantation. A matched pair analysis was performed to adjust for differences among groups. The final analysis was performed on 253 MUD and 95 haplo-HCT. In the matched cohort, median age at HCT was 11.2 and 10 years and median year of HCT was 2017 and 2018, in MUD and haplo-HCT recipients, respectively. The risk of grade III -IV acute graft - versus -host disease (aGVHD) was significantly higher in the haplo group (hazard ratio [HR]=2.33, 95% confidence interval [CI]: 1.18-4.58; P =0.01). No significant differences were found in 2 years overall survival (OS; 78.4% vs . 71.5%; HR=1.39, 95% CI: 0.84-2.31; P =0.19), leukemia -free survival (LFS; 72.7% vs . 69.5%; HR=1.22, 95% CI: 0.76-1.95; P =0.41), CI of relapse (RI; 19.3% vs . 19.5%; HR=1.14, 95% CI: 0.62-2.08; P =0.68) non -relapse -mortality (NRM; 8% vs. 11%; HR=1.39, 95% CI: 0.66-2.93; P =0.39) and graft - versus -host free relapse -free survival (GRFS; 60.7% vs . 54.5%, HR=1.38, 95% CI: 0.95-2.02; P =0.09) after MUD and haplo-HCT respectively. Our study suggests that haplo-HCT with PT-CY is a suitable option to transplant children with AML lacking a matched related donor.
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页码:2122 / 2130
页数:9
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