Indication and management of allogeneic haematopoietic stem-cell transplantation in myelofibrosis: updated recommendations by the EBMT/ELN International Working Group

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Indication and management of allogeneic haematopoietic stem-cell transplantation in myelofibrosis: updated recommendations by the EBMT/ELN International Working Group. / Kröger, Nicolaus; Bacigalupo, Andrea; Barbui, Tiziano; Ditschkowski, Markus; Gagelmann, Nico; Griesshammer, Martin; Gupta, Vikas; Hamad, Nada; Harrison, Claire; Hernandez-Boluda, Juan Carlos; Koschmieder, Steffen; Jain, Tania; Mascarenhas, John; Mesa, Ruben; Popat, Uday R; Passamonti, Francesco; Polverelli, Nicola; Rambaldi, Alessandro; Robin, Marie; Salit, Rachel B; Scott, Bart L; Tamari, Roni; Tefferi, Ayalew; Vannucchi, Alessandro M; McLornan, Donal P; Barosi, Giovanni.

In: LANCET HAEMATOL, Vol. 11, No. 1, 01.2024, p. e62-e74.

Research output: SCORING: Contribution to journalSCORING: Review articleResearch

Harvard

Kröger, N, Bacigalupo, A, Barbui, T, Ditschkowski, M, Gagelmann, N, Griesshammer, M, Gupta, V, Hamad, N, Harrison, C, Hernandez-Boluda, JC, Koschmieder, S, Jain, T, Mascarenhas, J, Mesa, R, Popat, UR, Passamonti, F, Polverelli, N, Rambaldi, A, Robin, M, Salit, RB, Scott, BL, Tamari, R, Tefferi, A, Vannucchi, AM, McLornan, DP & Barosi, G 2024, 'Indication and management of allogeneic haematopoietic stem-cell transplantation in myelofibrosis: updated recommendations by the EBMT/ELN International Working Group', LANCET HAEMATOL, vol. 11, no. 1, pp. e62-e74. https://doi.org/10.1016/S2352-3026(23)00305-8

APA

Kröger, N., Bacigalupo, A., Barbui, T., Ditschkowski, M., Gagelmann, N., Griesshammer, M., Gupta, V., Hamad, N., Harrison, C., Hernandez-Boluda, J. C., Koschmieder, S., Jain, T., Mascarenhas, J., Mesa, R., Popat, U. R., Passamonti, F., Polverelli, N., Rambaldi, A., Robin, M., ... Barosi, G. (2024). Indication and management of allogeneic haematopoietic stem-cell transplantation in myelofibrosis: updated recommendations by the EBMT/ELN International Working Group. LANCET HAEMATOL, 11(1), e62-e74. https://doi.org/10.1016/S2352-3026(23)00305-8

Vancouver

Bibtex

@article{2d43ceb170c24f188c91a185ae82be5a,
title = "Indication and management of allogeneic haematopoietic stem-cell transplantation in myelofibrosis: updated recommendations by the EBMT/ELN International Working Group",
abstract = "New options for medical therapy and risk scoring systems containing molecular data are leading to increased complexity in the management of patients with myelofibrosis. To inform patients' optimal care, we updated the 2015 guidelines on indications for and management of allogeneic haematopoietic stem-cell transplantation (HSCT) with the support of the European Society for Blood and Marrow Transplantation (EBMT) and European LeukemiaNet (ELN). New recommendations were produced using a consensus-building methodology after a comprehensive review of articles released from January, 2015 to December, 2022. Seven domains and 18 key questions were selected through a series of questionnaires using a Delphi process. Key recommendations in this update include: patients with primary myelofibrosis and an intermediate-2 or high-risk Dynamic International Prognostic Scoring System score, or a high-risk Mutation-Enhanced International Prognostic Score Systems (MIPSS70 or MIPSS70-plus) score, or a low-risk or intermediate-risk Myelofibrosis Transplant Scoring System score should be considered candidates for allogeneic HSCT. All patients who are candidates for allogeneic HSCT with splenomegaly greater than 5 cm below the left costal margin or splenomegaly-related symptoms should receive a spleen-directed treatment, ideally with a JAK-inhibitor; HLA-matched sibling donors remain the preferred donor source to date. Reduced intensity conditioning and myeloablative conditioning are both valid options for patients with myelofibrosis. Regular post-transplantation driver mutation monitoring is recommended to detect and treat early relapse with donor lymphocyte infusion. In a disease where evidence-based guidance is scarce, these recommendations might help clinicians and patients in shared decision making.",
author = "Nicolaus Kr{\"o}ger and Andrea Bacigalupo and Tiziano Barbui and Markus Ditschkowski and Nico Gagelmann and Martin Griesshammer and Vikas Gupta and Nada Hamad and Claire Harrison and Hernandez-Boluda, {Juan Carlos} and Steffen Koschmieder and Tania Jain and John Mascarenhas and Ruben Mesa and Popat, {Uday R} and Francesco Passamonti and Nicola Polverelli and Alessandro Rambaldi and Marie Robin and Salit, {Rachel B} and Scott, {Bart L} and Roni Tamari and Ayalew Tefferi and Vannucchi, {Alessandro M} and McLornan, {Donal P} and Giovanni Barosi",
note = "Copyright {\textcopyright} 2023 Elsevier Ltd. All rights reserved.",
year = "2024",
month = jan,
doi = "10.1016/S2352-3026(23)00305-8",
language = "English",
volume = "11",
pages = "e62--e74",
journal = "LANCET HAEMATOL",
issn = "2352-3026",
publisher = "Lancet Publishing Group",
number = "1",

}

RIS

TY - JOUR

T1 - Indication and management of allogeneic haematopoietic stem-cell transplantation in myelofibrosis: updated recommendations by the EBMT/ELN International Working Group

AU - Kröger, Nicolaus

AU - Bacigalupo, Andrea

AU - Barbui, Tiziano

AU - Ditschkowski, Markus

AU - Gagelmann, Nico

AU - Griesshammer, Martin

AU - Gupta, Vikas

AU - Hamad, Nada

AU - Harrison, Claire

AU - Hernandez-Boluda, Juan Carlos

AU - Koschmieder, Steffen

AU - Jain, Tania

AU - Mascarenhas, John

AU - Mesa, Ruben

AU - Popat, Uday R

AU - Passamonti, Francesco

AU - Polverelli, Nicola

AU - Rambaldi, Alessandro

AU - Robin, Marie

AU - Salit, Rachel B

AU - Scott, Bart L

AU - Tamari, Roni

AU - Tefferi, Ayalew

AU - Vannucchi, Alessandro M

AU - McLornan, Donal P

AU - Barosi, Giovanni

N1 - Copyright © 2023 Elsevier Ltd. All rights reserved.

PY - 2024/1

Y1 - 2024/1

N2 - New options for medical therapy and risk scoring systems containing molecular data are leading to increased complexity in the management of patients with myelofibrosis. To inform patients' optimal care, we updated the 2015 guidelines on indications for and management of allogeneic haematopoietic stem-cell transplantation (HSCT) with the support of the European Society for Blood and Marrow Transplantation (EBMT) and European LeukemiaNet (ELN). New recommendations were produced using a consensus-building methodology after a comprehensive review of articles released from January, 2015 to December, 2022. Seven domains and 18 key questions were selected through a series of questionnaires using a Delphi process. Key recommendations in this update include: patients with primary myelofibrosis and an intermediate-2 or high-risk Dynamic International Prognostic Scoring System score, or a high-risk Mutation-Enhanced International Prognostic Score Systems (MIPSS70 or MIPSS70-plus) score, or a low-risk or intermediate-risk Myelofibrosis Transplant Scoring System score should be considered candidates for allogeneic HSCT. All patients who are candidates for allogeneic HSCT with splenomegaly greater than 5 cm below the left costal margin or splenomegaly-related symptoms should receive a spleen-directed treatment, ideally with a JAK-inhibitor; HLA-matched sibling donors remain the preferred donor source to date. Reduced intensity conditioning and myeloablative conditioning are both valid options for patients with myelofibrosis. Regular post-transplantation driver mutation monitoring is recommended to detect and treat early relapse with donor lymphocyte infusion. In a disease where evidence-based guidance is scarce, these recommendations might help clinicians and patients in shared decision making.

AB - New options for medical therapy and risk scoring systems containing molecular data are leading to increased complexity in the management of patients with myelofibrosis. To inform patients' optimal care, we updated the 2015 guidelines on indications for and management of allogeneic haematopoietic stem-cell transplantation (HSCT) with the support of the European Society for Blood and Marrow Transplantation (EBMT) and European LeukemiaNet (ELN). New recommendations were produced using a consensus-building methodology after a comprehensive review of articles released from January, 2015 to December, 2022. Seven domains and 18 key questions were selected through a series of questionnaires using a Delphi process. Key recommendations in this update include: patients with primary myelofibrosis and an intermediate-2 or high-risk Dynamic International Prognostic Scoring System score, or a high-risk Mutation-Enhanced International Prognostic Score Systems (MIPSS70 or MIPSS70-plus) score, or a low-risk or intermediate-risk Myelofibrosis Transplant Scoring System score should be considered candidates for allogeneic HSCT. All patients who are candidates for allogeneic HSCT with splenomegaly greater than 5 cm below the left costal margin or splenomegaly-related symptoms should receive a spleen-directed treatment, ideally with a JAK-inhibitor; HLA-matched sibling donors remain the preferred donor source to date. Reduced intensity conditioning and myeloablative conditioning are both valid options for patients with myelofibrosis. Regular post-transplantation driver mutation monitoring is recommended to detect and treat early relapse with donor lymphocyte infusion. In a disease where evidence-based guidance is scarce, these recommendations might help clinicians and patients in shared decision making.

U2 - 10.1016/S2352-3026(23)00305-8

DO - 10.1016/S2352-3026(23)00305-8

M3 - SCORING: Review article

C2 - 38061384

VL - 11

SP - e62-e74

JO - LANCET HAEMATOL

JF - LANCET HAEMATOL

SN - 2352-3026

IS - 1

ER -