Abstract

Factors predicting allogeneic hematopoietic cell transplantation (HCT) outcomes in myelofibrosis in the early post-HCT period have not been defined thus far. We attempt to study such factors that can help identify patients at a higher risk of relapse or death. This retrospective study included 79 patients who underwent first HCT for myelofibrosis at three centers between 2005 and 2016. Univariate analysis showed that red blood cell (RBC) transfusion dependence (HR 9.02, 95% CI 4.0–20.35), platelet transfusion dependence (HR 8.17, 95%CI 3.83–17.37), 100% donor chimerism in CD33 + cells (HR 0.21, 95%CI 0.07–0.62), unfavorable molecular status (HR 4.41, 95%CI 1.87–10.39), normal spleen size (HR 0.42, 95%CI 0.19–0.94), grade ≥ 2 bone marrow fibrosis (vs. grade ≤ 1; HR 2.7, 95%CI 1.1–6.93) and poor graft function (HR 2.6, 95%CI 1.22–5.53) at day +100 were statistically significantly associated with relapse-free survival (RFS). RBC transfusion dependence and unfavorable molecular status were also statistically significant in the multivariate analysis. Patients in whom both of these factors were present had a significantly worse RFS when compared to those with one or none. While limited by a small sample size, we demonstrate the significance of transfusion dependence and molecular status at day +100 in predicting outcomes.

Details

Title
Early post-transplantation factors predict survival outcomes in patients undergoing allogeneic hematopoietic cell transplantation for myelofibrosis
Author
Jain, Tania 1   VIAFID ORCID Logo  ; Kunze, Katie L 2   VIAFID ORCID Logo  ; Mountjoy Luke 3 ; Partain, Daniel K 4 ; Kosiorek Heidi 2 ; Khera Nandita 3 ; Hogan, William J 5   VIAFID ORCID Logo  ; Roy, Vivek 6 ; Slack, James L 3 ; Noel, Pierre 3 ; Fauble Veena D S 7 ; Leis, Jose F 3 ; Sproat, Lisa 3 ; Tefferi Ayalew 5 ; Patnaik, Mrinal M 5 ; Mesa, Ruben A 8 ; Palmer, Jeanne 3 

 Mayo Clinic, Division of Hematology and Medical Oncology, Phoenix, USA (GRID:grid.417468.8) (ISNI:0000 0000 8875 6339); Johns Hopkins University School of Medicine, Hematologic Malignancies and Bone Marrow Transplantation Program, Baltimore, USA (GRID:grid.21107.35) (ISNI:0000 0001 2171 9311) 
 Division of Biomedical Statistical and Informatics, Department of Health Sciences Research, Mayo Clinic, Phoenix, USA (GRID:grid.417468.8) (ISNI:0000 0000 8875 6339) 
 Mayo Clinic, Division of Hematology and Medical Oncology, Phoenix, USA (GRID:grid.417468.8) (ISNI:0000 0000 8875 6339) 
 Mayo Clinic, Division of General Internal Medicine, Rochester, USA (GRID:grid.66875.3a) (ISNI:0000 0004 0459 167X); Mayo Clinic, Center for Palliative Medicine, Rochester, USA (GRID:grid.66875.3a) (ISNI:0000 0004 0459 167X) 
 Mayo Clinic, Division of Hematology and Bone Marrow Transplant, Rochester, USA (GRID:grid.66875.3a) (ISNI:0000 0004 0459 167X) 
 Mayo Clinic, Division of Hematology and Medical Oncology, Jacksonville, USA (GRID:grid.417467.7) (ISNI:0000 0004 0443 9942) 
 Honor Health Cancer Care Network, Scottsdale, USA (GRID:grid.417468.8) 
 University of Texas Health San Antonio Cancer Center, San Antonio, USA (GRID:grid.215352.2) (ISNI:0000000121845633) 
Publication year
2020
Publication date
Mar 2020
Publisher
Springer Nature B.V.
e-ISSN
20445385
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2375798059
Copyright
This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.