Allogeneic hematopoietic cell transplantation in older myelofibrosis patients: A study of the chronic malignancies working party of EBMT and the Spanish Myelofibrosis Registry

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Allogeneic hematopoietic cell transplantation in older myelofibrosis patients: A study of the chronic malignancies working party of EBMT and the Spanish Myelofibrosis Registry. / Hernández-Boluda, Juan-Carlos; Pereira, Arturo; Kröger, Nicolaus; Cornelissen, Jan J; Beelen, Dietrich; de Witte, Moniek; Wilson, Keith; Platzbecker, Uwe; Sengeloev, Henrik; Blaise, Didier; Einsele, Hermann; Sockel, Katja; Krüger, William; Lenhoff, Stig; Salaroli, Adriano; Martin, Hans; García-Gutiérrez, Valentín; Pavone, Vicenzo; Alvarez-Larrán, Alberto; Raya, José-María; Zinger, Nienke; Gras, Luuk; Hayden, Patrick; Czerw, Tomasz; P McLornan, Donal; Yakoub-Agha, Ibrahim.

in: AM J HEMATOL, Jahrgang 96, Nr. 10, 01.10.2021, S. 1186-1194.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Hernández-Boluda, J-C, Pereira, A, Kröger, N, Cornelissen, JJ, Beelen, D, de Witte, M, Wilson, K, Platzbecker, U, Sengeloev, H, Blaise, D, Einsele, H, Sockel, K, Krüger, W, Lenhoff, S, Salaroli, A, Martin, H, García-Gutiérrez, V, Pavone, V, Alvarez-Larrán, A, Raya, J-M, Zinger, N, Gras, L, Hayden, P, Czerw, T, P McLornan, D & Yakoub-Agha, I 2021, 'Allogeneic hematopoietic cell transplantation in older myelofibrosis patients: A study of the chronic malignancies working party of EBMT and the Spanish Myelofibrosis Registry', AM J HEMATOL, Jg. 96, Nr. 10, S. 1186-1194. https://doi.org/10.1002/ajh.26279

APA

Hernández-Boluda, J-C., Pereira, A., Kröger, N., Cornelissen, J. J., Beelen, D., de Witte, M., Wilson, K., Platzbecker, U., Sengeloev, H., Blaise, D., Einsele, H., Sockel, K., Krüger, W., Lenhoff, S., Salaroli, A., Martin, H., García-Gutiérrez, V., Pavone, V., Alvarez-Larrán, A., ... Yakoub-Agha, I. (2021). Allogeneic hematopoietic cell transplantation in older myelofibrosis patients: A study of the chronic malignancies working party of EBMT and the Spanish Myelofibrosis Registry. AM J HEMATOL, 96(10), 1186-1194. https://doi.org/10.1002/ajh.26279

Vancouver

Bibtex

@article{9af6033c626549c5be68e3944834bd0a,
title = "Allogeneic hematopoietic cell transplantation in older myelofibrosis patients: A study of the chronic malignancies working party of EBMT and the Spanish Myelofibrosis Registry",
abstract = "Allogeneic hematopoietic cell transplantation (allo-HCT) is increasingly used in older myelofibrosis (MF) patients, but its risk/benefit ratio compared to non-transplant approaches has not been evaluated in this population. We analyzed the outcomes of allo-HCT in 556 MF patients aged ≥65 years from the EBMT registry, and determined the excess mortality over the matched general population of MF patients ≥65 years managed with allo-HCT (n = 556) or conventional drug treatment (n = 176). The non-transplant cohort included patients with intermediate-2 or high risk DIPSS from the Spanish Myelofibrosis Registry. After a median follow-up of 3.4 years, the estimated 5-year survival rate, non-relapse mortality (NRM), and relapse incidence after transplantation was 40%, 37%, and 25%, respectively. Busulfan-based conditioning was associated with decreased mortality (HR: 0.7, 95% CI: 0.5-0.9) whereas the recipient CMV+/donor CMV- combination (HR: 1.7, 95% CI: 1.2-2.4) and the JAK2 mutated genotype (HR: 1.9, 95% CI: 1.1-3.5) predicted higher mortality. Busulfan-based conditioning correlated with improved survival due to less NRM, despite its higher relapse rate when compared with melphalan-based regimens. Excess mortality was higher in transplanted patients than in the non-HCT cohort in the first year of follow-up (ratio: 1.93, 95% CI: 1.13-2.80), whereas the opposite occurred between the fourth and eighth follow-up years (ratio: 0.31, 95% CI: 0.18-0.53). Comparing the excess mortality of the two treatments, male patients seemed to benefit more than females from allo-HCT, mainly due to their worse prognosis with non-transplant approaches. These findings could potentially enhance counseling and treatment decision-making in elderly transplant-eligible MF patients.",
keywords = "Age Factors, Aged, Cohort Studies, Female, Hematopoietic Stem Cell Transplantation, Humans, Male, Primary Myelofibrosis/epidemiology, Registries, Spain/epidemiology, Survival Analysis, Transplantation, Homologous",
author = "Juan-Carlos Hern{\'a}ndez-Boluda and Arturo Pereira and Nicolaus Kr{\"o}ger and Cornelissen, {Jan J} and Dietrich Beelen and {de Witte}, Moniek and Keith Wilson and Uwe Platzbecker and Henrik Sengeloev and Didier Blaise and Hermann Einsele and Katja Sockel and William Kr{\"u}ger and Stig Lenhoff and Adriano Salaroli and Hans Martin and Valent{\'i}n Garc{\'i}a-Guti{\'e}rrez and Vicenzo Pavone and Alberto Alvarez-Larr{\'a}n and Jos{\'e}-Mar{\'i}a Raya and Nienke Zinger and Luuk Gras and Patrick Hayden and Tomasz Czerw and {P McLornan}, Donal and Ibrahim Yakoub-Agha",
note = "{\textcopyright} 2021 The Authors. American Journal of Hematology published by Wiley Periodicals LLC.",
year = "2021",
month = oct,
day = "1",
doi = "10.1002/ajh.26279",
language = "English",
volume = "96",
pages = "1186--1194",
journal = "AM J HEMATOL",
issn = "0361-8609",
publisher = "Wiley-Liss Inc.",
number = "10",

}

RIS

TY - JOUR

T1 - Allogeneic hematopoietic cell transplantation in older myelofibrosis patients: A study of the chronic malignancies working party of EBMT and the Spanish Myelofibrosis Registry

AU - Hernández-Boluda, Juan-Carlos

AU - Pereira, Arturo

AU - Kröger, Nicolaus

AU - Cornelissen, Jan J

AU - Beelen, Dietrich

AU - de Witte, Moniek

AU - Wilson, Keith

AU - Platzbecker, Uwe

AU - Sengeloev, Henrik

AU - Blaise, Didier

AU - Einsele, Hermann

AU - Sockel, Katja

AU - Krüger, William

AU - Lenhoff, Stig

AU - Salaroli, Adriano

AU - Martin, Hans

AU - García-Gutiérrez, Valentín

AU - Pavone, Vicenzo

AU - Alvarez-Larrán, Alberto

AU - Raya, José-María

AU - Zinger, Nienke

AU - Gras, Luuk

AU - Hayden, Patrick

AU - Czerw, Tomasz

AU - P McLornan, Donal

AU - Yakoub-Agha, Ibrahim

N1 - © 2021 The Authors. American Journal of Hematology published by Wiley Periodicals LLC.

PY - 2021/10/1

Y1 - 2021/10/1

N2 - Allogeneic hematopoietic cell transplantation (allo-HCT) is increasingly used in older myelofibrosis (MF) patients, but its risk/benefit ratio compared to non-transplant approaches has not been evaluated in this population. We analyzed the outcomes of allo-HCT in 556 MF patients aged ≥65 years from the EBMT registry, and determined the excess mortality over the matched general population of MF patients ≥65 years managed with allo-HCT (n = 556) or conventional drug treatment (n = 176). The non-transplant cohort included patients with intermediate-2 or high risk DIPSS from the Spanish Myelofibrosis Registry. After a median follow-up of 3.4 years, the estimated 5-year survival rate, non-relapse mortality (NRM), and relapse incidence after transplantation was 40%, 37%, and 25%, respectively. Busulfan-based conditioning was associated with decreased mortality (HR: 0.7, 95% CI: 0.5-0.9) whereas the recipient CMV+/donor CMV- combination (HR: 1.7, 95% CI: 1.2-2.4) and the JAK2 mutated genotype (HR: 1.9, 95% CI: 1.1-3.5) predicted higher mortality. Busulfan-based conditioning correlated with improved survival due to less NRM, despite its higher relapse rate when compared with melphalan-based regimens. Excess mortality was higher in transplanted patients than in the non-HCT cohort in the first year of follow-up (ratio: 1.93, 95% CI: 1.13-2.80), whereas the opposite occurred between the fourth and eighth follow-up years (ratio: 0.31, 95% CI: 0.18-0.53). Comparing the excess mortality of the two treatments, male patients seemed to benefit more than females from allo-HCT, mainly due to their worse prognosis with non-transplant approaches. These findings could potentially enhance counseling and treatment decision-making in elderly transplant-eligible MF patients.

AB - Allogeneic hematopoietic cell transplantation (allo-HCT) is increasingly used in older myelofibrosis (MF) patients, but its risk/benefit ratio compared to non-transplant approaches has not been evaluated in this population. We analyzed the outcomes of allo-HCT in 556 MF patients aged ≥65 years from the EBMT registry, and determined the excess mortality over the matched general population of MF patients ≥65 years managed with allo-HCT (n = 556) or conventional drug treatment (n = 176). The non-transplant cohort included patients with intermediate-2 or high risk DIPSS from the Spanish Myelofibrosis Registry. After a median follow-up of 3.4 years, the estimated 5-year survival rate, non-relapse mortality (NRM), and relapse incidence after transplantation was 40%, 37%, and 25%, respectively. Busulfan-based conditioning was associated with decreased mortality (HR: 0.7, 95% CI: 0.5-0.9) whereas the recipient CMV+/donor CMV- combination (HR: 1.7, 95% CI: 1.2-2.4) and the JAK2 mutated genotype (HR: 1.9, 95% CI: 1.1-3.5) predicted higher mortality. Busulfan-based conditioning correlated with improved survival due to less NRM, despite its higher relapse rate when compared with melphalan-based regimens. Excess mortality was higher in transplanted patients than in the non-HCT cohort in the first year of follow-up (ratio: 1.93, 95% CI: 1.13-2.80), whereas the opposite occurred between the fourth and eighth follow-up years (ratio: 0.31, 95% CI: 0.18-0.53). Comparing the excess mortality of the two treatments, male patients seemed to benefit more than females from allo-HCT, mainly due to their worse prognosis with non-transplant approaches. These findings could potentially enhance counseling and treatment decision-making in elderly transplant-eligible MF patients.

KW - Age Factors

KW - Aged

KW - Cohort Studies

KW - Female

KW - Hematopoietic Stem Cell Transplantation

KW - Humans

KW - Male

KW - Primary Myelofibrosis/epidemiology

KW - Registries

KW - Spain/epidemiology

KW - Survival Analysis

KW - Transplantation, Homologous

U2 - 10.1002/ajh.26279

DO - 10.1002/ajh.26279

M3 - SCORING: Journal article

C2 - 34152630

VL - 96

SP - 1186

EP - 1194

JO - AM J HEMATOL

JF - AM J HEMATOL

SN - 0361-8609

IS - 10

ER -