Allogenic haematopoietic cell transplantation for myelofibrosis: proposed definitions and management strategies for graft failure, poor graft function and relapse: best practice recommendations of the EBMT Chronic Malignancies Working Party
Allogenic haematopoietic cell transplantation for myelofibrosis: proposed definitions and management strategies for graft failure, poor graft function and relapse: best practice recommendations of the EBMT Chronic Malignancies Working Party
Allogeneic Haematopoietic Cell Transplantation (allo-HCT) remains the only curative approach in Myelofibrosis (MF). Despite advances over recent decades, relapse and non-relapse mortality rates remain significant. Relapse rates vary between 15% and 25% across retrospective studies and management strategies vary widely, ranging from palliation to adoptive immunotherapy and, in some cases, a second allo-HCT. Moreover, in allo-HCT, there is a higher incidence of poor graft function and graft failure due to splenomegaly and a hostile ‘pro-inflammatory’ marrow niche. The Practice Harmonisation and Guidelines subcommittee of the Chronic Malignancies Working Party (CMWP) of EBMT convened an international panel consisting of transplant haematologists, histopathologists and molecular biologists to propose practical, clinically relevant definitions of graft failure, poor graft function and relapse as well as management strategies following allo-HCT. A systematic approach to molecular monitoring, histopathological assessment and chimerism testing is proposed. These proposed recommendations aim to increase the accuracy and uniformity of reporting and to thereby facilitate the development of more consistent approaches to these challenging issues. In addition, we propose management strategies for these complications.
2445-2459
Mclornan, Donal P.
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Hernandez Boluda, Juan Carlos
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Czerw, Tomasz
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Cross, Nicholas
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Deeg, H.J.
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Ditschkowski, Marcus
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Moonim, M.
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Polverelli, Nicola
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Robin, Marie
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Aljurf, Mahmoud
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Conneally, Eibhlin
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Hayden, Patrick
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Yakoub-Agha, Ibrahim
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September 2021
Mclornan, Donal P.
25a8b0c7-de6b-4b40-bf70-e2db5ecf4002
Hernandez Boluda, Juan Carlos
ed9707fd-4e15-4903-8b35-4dc14c0ea735
Czerw, Tomasz
4a9bf539-9ebd-4e9a-b751-f14f07946629
Cross, Nicholas
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Deeg, H.J.
e9db65d8-df4c-450f-95d7-f974657e5502
Ditschkowski, Marcus
69f4f3f0-a8ca-42c6-be93-f417cd7154d0
Moonim, M.
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Polverelli, Nicola
e8d70d09-d373-4115-8d09-b80c2589f284
Robin, Marie
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Aljurf, Mahmoud
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Conneally, Eibhlin
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Hayden, Patrick
d5e2e7c2-da6f-4a04-b9f6-8963fc20924f
Yakoub-Agha, Ibrahim
7f01d81f-64a9-49e5-8ade-df0976a0bf51
Mclornan, Donal P., Hernandez Boluda, Juan Carlos, Czerw, Tomasz, Cross, Nicholas, Deeg, H.J., Ditschkowski, Marcus, Moonim, M., Polverelli, Nicola, Robin, Marie, Aljurf, Mahmoud, Conneally, Eibhlin, Hayden, Patrick and Yakoub-Agha, Ibrahim
(2021)
Allogenic haematopoietic cell transplantation for myelofibrosis: proposed definitions and management strategies for graft failure, poor graft function and relapse: best practice recommendations of the EBMT Chronic Malignancies Working Party.
Leukemia, 35 (9), .
(doi:10.1038/s41375-021-01294-2).
Abstract
Allogeneic Haematopoietic Cell Transplantation (allo-HCT) remains the only curative approach in Myelofibrosis (MF). Despite advances over recent decades, relapse and non-relapse mortality rates remain significant. Relapse rates vary between 15% and 25% across retrospective studies and management strategies vary widely, ranging from palliation to adoptive immunotherapy and, in some cases, a second allo-HCT. Moreover, in allo-HCT, there is a higher incidence of poor graft function and graft failure due to splenomegaly and a hostile ‘pro-inflammatory’ marrow niche. The Practice Harmonisation and Guidelines subcommittee of the Chronic Malignancies Working Party (CMWP) of EBMT convened an international panel consisting of transplant haematologists, histopathologists and molecular biologists to propose practical, clinically relevant definitions of graft failure, poor graft function and relapse as well as management strategies following allo-HCT. A systematic approach to molecular monitoring, histopathological assessment and chimerism testing is proposed. These proposed recommendations aim to increase the accuracy and uniformity of reporting and to thereby facilitate the development of more consistent approaches to these challenging issues. In addition, we propose management strategies for these complications.
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Accepted/In Press date: 7 May 2021
Published date: September 2021
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© 2021, The Author(s), under exclusive licence to Springer Nature Limited.
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Local EPrints ID: 449197
URI: http://eprints.soton.ac.uk/id/eprint/449197
ISSN: 0887-6924
PURE UUID: 08bbc369-f73b-4a5b-be02-4da4eaaeeb93
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Date deposited: 19 May 2021 18:15
Last modified: 17 Mar 2024 06:33
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Contributors
Author:
Donal P. Mclornan
Author:
Juan Carlos Hernandez Boluda
Author:
Tomasz Czerw
Author:
H.J. Deeg
Author:
Marcus Ditschkowski
Author:
M. Moonim
Author:
Nicola Polverelli
Author:
Marie Robin
Author:
Mahmoud Aljurf
Author:
Eibhlin Conneally
Author:
Patrick Hayden
Author:
Ibrahim Yakoub-Agha
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