Impact of bone marrow fibrosis on outcomes of allogeneic hematopoietic stem cell transplantation in acute myeloid leukemia

Bone marrow fibrosis (BMF) of unknown etiology was common in hematological malignancies, but its prognostic value for acute myeloid leukemia (AML) is unclear. We interrogated data from 532 newly diagnosed subjects with AML receiving allogeneic hematological stem cell transplantation to evaluate the...

Full description

Saved in:
Bibliographic Details
Published inBone marrow transplantation (Basingstoke)
Main Authors Zhang, Haixiao, Guo, Wenwen, Wang, Jiali, Lu, Ni, Zheng, Xinhui, Sun, Qi, Xia, Yonghui, Zhang, Rongli, Chen, Xin, Ma, Qiaoling, Yang, Donglin, Pang, Aiming, Wei, Jialin, He, Yi, Feng, Sizhou, Han, Mingzhe, Zhai, Weihua, Jiang, Erlie
Format Journal Article
LanguageEnglish
Published England 27.08.2024
Online AccessGet full text

Cover

Loading…
More Information
Summary:Bone marrow fibrosis (BMF) of unknown etiology was common in hematological malignancies, but its prognostic value for acute myeloid leukemia (AML) is unclear. We interrogated data from 532 newly diagnosed subjects with AML receiving allogeneic hematological stem cell transplantation to evaluate the prognostic impact of BMF on transplant outcomes. Using the European consensus on the grading of BMF at diagnosis, 255 (48%) subjects were BMF-0, 209 (39%), BMF-1 and 68 (13%), BMF-2-3. Subjects with BMF-2-3 had poor overall survival (P < 0.001), disease-free survival (P < 0.001) and a higher incidence of relapse (CIR, P < 0.001). Multi-variable analyses in subjects achieving pre-transplant complete remission showed BMF-2-3 was an independent risk factor for CIR (Hazard Ratio [HR] = 2.17, (95% CI, 1.11, 4,24); P = 0.02). Furthermore, BMF-2-3 group showed delayed neutrophil and platelet engraftment and delayed B cell recovery post-transplantation. These findings demonstrate the significance of BMF in transplant outcomes and attract more attention to AML with BMF.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1476-5365
1476-5365
DOI:10.1038/s41409-024-02402-3