Impact of allele-level HLA matching on outcomes after double cord blood transplantation in adults with malignancies
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Tipo de produção
article
Data de publicação
2023
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ELSEVIER
Autores
VOLT, Fernanda
MOREIRA, Frederico
CONELISSEN, Jan
FURST, Sabine
DAGUINDAU, Etienne
SIRVENT, Anne
LATOUR, Regis Peffault de
RAFIL, Hanadi
Citação
BLOOD ADVANCES, v.7, n.13, p.3297-3306, 2023
Resumo
In single unrelated cord blood transplantation (UCBT), an increasing number of HLA allele mismatches (MM) has been associated with inferior overall survival (OS) and attributed to higher transplant-related mortality (TRM). Previous studies on the role of allele-level HLA matching after double UCBT (dUCBT) showed conflicting results. In this study, we report the impact of allele-level HLA matching on the outcomes of a large dUCBT cohort. We included 963 adults with hematologic malignancies, with available allele-level HLA matching at HLAA, -B, -C, and -DRB1, receiving dUCBT between 2006 to 2019. Assignment of donor-recipient HLA match was performed considering the unit with the highest disparity with the recipient. Three hundred ninety-two patients received dUCBT with 0 to 3 MM and 571 with >4 allele MM. For recipients of dUCBT with 0 to 3 MM, day-100 and 4-year TRM were 10% and 23%, respectively, compared with 16% and 36% for those with >4 MM. A higher degree of allele MM was also associated with the worse neutrophil recovery and lower incidence of relapse; no significant effect on graft-versus-host disease was observed. Patients receiving units with 0 to 3 MM had a 4-year OS of 54% compared with 43% for those receiving units with >4 MM. The inferior OS associated with higher HLA disparity was only partially mitigated by increased total nucleated cell doses. Our results confirm that allele-level HLA typing is a significant factor for OS after dUCBT, and units with >4 MM (<4/8 HLA-matched) should be avoided if possible.
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Referências
- Armand P, 2014, BLOOD, V123, P3664, DOI 10.1182/blood-2014-01-552984
- Bacigalupo A, 2009, BIOL BLOOD MARROW TR, V15, P1628, DOI 10.1016/j.bbmt.2009.07.004
- Barker JN, 2020, BLOOD ADV, V4, P6064, DOI 10.1182/bloodadvances.2020003371
- Barker JN, 2017, BIOL BLOOD MARROW TR, V23, P882, DOI 10.1016/j.bbmt.2017.03.006
- Baron F, 2017, J HEMATOL ONCOL, V10, DOI 10.1186/s13045-017-0497-9
- Brunstein C, 2017, HAEMATOLOGICA, V102, P941, DOI 10.3324/haematol.2016.158584
- Brunstein CG, 2016, BIOL BLOOD MARROW TR, V22, P487, DOI 10.1016/j.bbmt.2015.09.025
- Contal C, 1999, COMPUT STAT DATA AN, V30, P253, DOI 10.1016/S0167-9473(98)00096-6
- Cornelissen Jan J, 2017, Stem Cell Investig, V4, P47, DOI 10.21037/sci.2017.05.09
- Dahi PB, 2014, BONE MARROW TRANSPL, V49, P1184, DOI 10.1038/bmt.2014.135
- Dehn J, 2019, BLOOD, V132, P924, DOI 10.1182/blood.2019001212
- Delaney M, 2009, TRANSFUSION, V49, P995, DOI 10.1111/j.1537-2995.2008.02077.x
- Eapen M, 2017, LANCET HAEMATOL, V4, pE325, DOI 10.1016/S2352-3026(17)30104-7
- Eapen M, 2014, BLOOD, V123, P133, DOI 10.1182/blood-2013-05-506253
- Fatobene G, 2020, BLOOD ADV, V4, P6327, DOI 10.1182/bloodadvances.2020002258
- Fatobene G, 2020, J CLIN ONCOL, V38, P1518, DOI 10.1200/JCO.19.02408
- Fine JP, 1999, J AM STAT ASSOC, V94, P496, DOI 10.2307/2670170
- Fuchs EJ, 2022, BLOOD, V139, P1452, DOI 10.1182/blood.2021013443
- Fuchs EJ, 2021, BLOOD, V137, P420, DOI 10.1182/blood.2020007535
- Gluckman E, 2004, EXP HEMATOL, V32, P397, DOI 10.1016/j.exphem.2004.01.002
- Horwitz ME, 2021, BLOOD, V138, P1429, DOI 10.1182/blood.2021011719
- Iemura T, 2020, SCI REP-UK, V10, DOI 10.1038/s41598-020-78259-5
- Jagasia MH, 2015, BIOL BLOOD MARROW TR, V21, P389, DOI 10.1016/j.bbmt.2014.12.001
- Kalbfleisch J.D., 1980, STAT ANAL FAILURE TI
- Kindwall-Keller TL, 2012, BONE MARROW TRANSPL, V47, P924, DOI 10.1038/bmt.2011.195
- Lamers CHJ, 2016, BLOOD, V128, P2165, DOI 10.1182/blood-2016-06-718619
- Lau C, 2019, BIOL BLOOD MARROW TR, V25, pS94, DOI 10.1016/j.bbmt.2018.12.182
- Lee SJ, 2007, BLOOD, V110, P4576, DOI 10.1182/blood-2007-06-097386
- Mallhi KK, 2017, BIOL BLOOD MARROW TR, V23, P119, DOI 10.1016/j.bbmt.2016.10.019
- Michel G, 2016, BLOOD, V127, P3450, DOI 10.1182/blood-2016-01-694349
- Milano F, 2020, BLOOD ADV, V4, P3302, DOI 10.1182/bloodadvances.2020002222
- Milano F, 2017, BLOOD, V130, P1480, DOI 10.1182/blood-2017-06-788513
- Morishima Y, 2015, BLOOD, V125, P1189, DOI 10.1182/blood-2014-10-604785
- Olson AL, 2021, TRANSPL CELL THER, V27, P359, DOI 10.1016/j.jtct.2021.01.024
- Oran B, 2015, HAEMATOLOGICA, V100, P1361, DOI 10.3324/haematol.2015.127787
- Politikos I, 2022, BLOOD ADV, V6, P6291, DOI 10.1182/bloodadvances.2022008047
- Purtill D, 2015, BIOL BLOOD MARROW TR, V21, P1981, DOI 10.1016/j.bbmt.2015.07.015
- Purtill D, 2014, BLOOD, V124, P2905, DOI 10.1182/blood-2014-03-566216
- Rowlings PA, 1997, BRIT J HAEMATOL, V97, P855, DOI 10.1046/j.1365-2141.1997.1112925.x
- Ruggeri A, 2014, LEUKEMIA, V28, P779, DOI 10.1038/leu.2013.259
- Ruggeri A, 2019, HEMATOL-AM SOC HEMAT, P522, DOI 10.1182/hematology.2019000056
- SAS Institute Inc, 2018, SAS STAT 151 US GUID
- Tozatto-Maio K, 2018, BIOL BLOOD MARROW TR, V24, P1657, DOI 10.1016/j.bbmt.2018.02.014
- Verneris MR, 2009, BLOOD, V114, P4293, DOI 10.1182/blood-2009-05-220525
- Wagner JE, 2014, NEW ENGL J MED, V371, P1685, DOI 10.1056/NEJMoa1405584
- Watkins B, 2021, J CLIN ONCOL, V39, P1865, DOI 10.1200/JCO.20.01086
- Yabe T, 2018, LEUKEMIA, V32, P168, DOI 10.1038/leu.2017.202
- Yokoyama H, 2020, BIOL BLOOD MARROW TR, V26, P519, DOI 10.1016/j.bbmt.2019.11.001