TY - JOUR
T1 - A simple prognostic system in patients with myelofibrosis undergoing allogeneic stem cell transplantation
T2 - a CIBMTR/EBMT analysis
AU - Tamari, Roni
AU - McLornan, Donal P.
AU - Ahn, Kwang Woo
AU - Estrada-Merly, Noel
AU - Hernández-Boluda, Juan Carlos
AU - Giralt, Sergio
AU - Palmer, Jeanne
AU - Gale, Robert Peter
AU - DeFilipp, Zachariah
AU - Marks, David I.
AU - van der Poel, Marjolein
AU - Verdonck, Leo F.
AU - Battiwalla, Minoo
AU - Diaz, Miguel Angel
AU - Gupta, Vikas
AU - Ali, Haris
AU - Litzow, Mark Robert
AU - Lazarus, Hillard M.
AU - Gergis, Usama
AU - Bashey, Asad
AU - Liesveld, Jane
AU - Hashmi, Shahrukh
AU - Pu, Jeffrey J.
AU - Beitinjaneh, Amer
AU - Bredeson, Christopher
AU - Rizzieri, David
AU - Savani, Bipin N.
AU - Abid, Muhammad Bilal
AU - Ganguly, Siddhartha
AU - Agrawal, Vaibhav
AU - Bacher, Vera Ulrike
AU - Wirk, Baldeep
AU - Jain, Tania
AU - Cutler, Corey
AU - Aljurf, Mahmoud
AU - Kindwall-Keller, Tamila
AU - Kharfan-Dabaja, Mohamed A.
AU - Hildebrandt, Gerhard C.
AU - Pawarode, Attaphol
AU - Solh, Melhem M.
AU - Yared, Jean A.
AU - Grunwald, Michael R.
AU - Nathan, Sunita
AU - Nishihori, Taiga
AU - Seo, Sachiko
AU - Scott, Bart L.
AU - Nakamura, Ryotaro
AU - Oran, Betul
AU - Czerw, Tomasz
AU - Yakoub-Agha, Ibrahim
AU - Saber, Wael
N1 - Publisher Copyright:
© 2023 by The American Society of Hematology. Licensed under Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0), permitting only noncommercial, nonderivative use with attribution. All other rights reserved.
PY - 2023/8/8
Y1 - 2023/8/8
N2 - To develop a prognostic model for patients undergoing allogeneic hematopoietic cell transplantation (allo-HCT) for myelofibrosis (MF), we examined the data of 623 patients undergoing allo-HCT between 2000 and 2016 in the United States (the Center for International Blood and Marrow Transplant Research [CIBMTR] cohort). A Cox multivariable model was used to identify factors prognostic of mortality. A weighted score using these factors was assigned to patients who received transplantation in Europe (the European Bone Marrow Transplant [EBMT] cohort; n = 623). Patient age >50 years (hazard ratio [HR], 1.39; 95% confidence interval [CI], 0.98-1.96), and HLA-matched unrelated donor (HR, 1.29; 95% CI, 0.98-1.7) were associated with an increased hazard of death and were assigned 1 point. Hemoglobin levels <100 g/L at time of transplantation (HR, 1.63; 95% CI, 1.2-2.19) and a mismatched unrelated donor (HR, 1.78; 95% CI, 1.25-2.52) were assigned 2 points. The 3-year overall survival (OS) in patients with a low (1-2 points), intermediate (3-4 points), and high score (5 points) were 69% (95% CI, 61-76), 51% (95% CI, 46-56.4), and 34% (95% CI, 21-49), respectively (P < .001). Increasing score was predictive of increased transplant-related mortality (TRM; P = .0017) but not of relapse (P = .12). The derived score was predictive of OS (P < .001) and TRM (P = .002) but not of relapse (P = .17) in the EBMT cohort as well. The proposed system was prognostic of survival in 2 large cohorts, CIBMTR and EBMT, and can easily be applied by clinicians consulting patients with MF about the transplantation outcomes.
AB - To develop a prognostic model for patients undergoing allogeneic hematopoietic cell transplantation (allo-HCT) for myelofibrosis (MF), we examined the data of 623 patients undergoing allo-HCT between 2000 and 2016 in the United States (the Center for International Blood and Marrow Transplant Research [CIBMTR] cohort). A Cox multivariable model was used to identify factors prognostic of mortality. A weighted score using these factors was assigned to patients who received transplantation in Europe (the European Bone Marrow Transplant [EBMT] cohort; n = 623). Patient age >50 years (hazard ratio [HR], 1.39; 95% confidence interval [CI], 0.98-1.96), and HLA-matched unrelated donor (HR, 1.29; 95% CI, 0.98-1.7) were associated with an increased hazard of death and were assigned 1 point. Hemoglobin levels <100 g/L at time of transplantation (HR, 1.63; 95% CI, 1.2-2.19) and a mismatched unrelated donor (HR, 1.78; 95% CI, 1.25-2.52) were assigned 2 points. The 3-year overall survival (OS) in patients with a low (1-2 points), intermediate (3-4 points), and high score (5 points) were 69% (95% CI, 61-76), 51% (95% CI, 46-56.4), and 34% (95% CI, 21-49), respectively (P < .001). Increasing score was predictive of increased transplant-related mortality (TRM; P = .0017) but not of relapse (P = .12). The derived score was predictive of OS (P < .001) and TRM (P = .002) but not of relapse (P = .17) in the EBMT cohort as well. The proposed system was prognostic of survival in 2 large cohorts, CIBMTR and EBMT, and can easily be applied by clinicians consulting patients with MF about the transplantation outcomes.
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U2 - 10.1182/bloodadvances.2023009886
DO - 10.1182/bloodadvances.2023009886
M3 - Article
C2 - 37134306
AN - SCOPUS:85164130120
SN - 2473-9529
VL - 7
SP - 3993
EP - 4002
JO - Blood Advances
JF - Blood Advances
IS - 15
ER -