TY - JOUR
T1 - Delayed platelet recovery after allogeneic hematopoietic stem cell transplantation
T2 - Association with chronic graft-versus-host disease and survival outcome
AU - Akahoshi, Yu
AU - Kimura, Shun Ichi
AU - Gomyo, Ayumi
AU - Hayakawa, Jin
AU - Tamaki, Masaharu
AU - Harada, Naonori
AU - Kusuda, Machiko
AU - Kameda, Kazuaki
AU - Ugai, Tomotaka
AU - Wada, Hidenori
AU - Ishihara, Yuko
AU - Kawamura, Koji
AU - Sakamoto, Kana
AU - Sato, Miki
AU - Terasako-Saito, Kiriko
AU - Kikuchi, Misato
AU - Nakasone, Hideki
AU - Kako, Shinichi
AU - Kanda, Yoshinobu
N1 - Publisher Copyright:
Copyright © 2017 John Wiley & Sons, Ltd.
PY - 2018/2
Y1 - 2018/2
N2 - Delayed platelet recovery (DPR) despite prompt neutrophil engraftment is frequently observed after allogeneic hematopoietic stem cell transplantation (HSCT). However, few studies have evaluated the risk factors and long-term outcome. Therefore, we retrospectively analysed 219 adult patients who underwent their first allogenic HSCT with neutrophil engraftment. Of these 219 patients, 50 (22.8%) had DPR that was defined as relapse-free survival at day 60 after HSCT without primary platelet recovery despite neutrophil engraftment. The results of a multivariate analysis showed that a high-risk underlying disease (odds ratio [OR], 2.38; 95% confidence interval [CI], 1.04-5.48; P =.041) and human leukocyte antigen–mismatched HSCT (OR, 2.63; 95% CI, 1.28-5.43; P =.009) were associated with an increased risk of DPR. In univariate analyses, the occurrence of DPR was significantly associated with inferior overall survival, high nonrelapse mortality, and a low incidence of chronic graft-versus-host disease (GVHD), despite a comparable relapse rate. In multivariate analyses, DPR was associated with inferior overall survival (hazard ratio [HR], 2.00; 95% CI, 1.23-3.27; P =.005) and a low incidence of chronic GVHD (HR, 0.42; 95% CI, 0.22-0.78; P =.002). In conclusion, DPR was a strong predictor of shorter survival but also less frequent chronic GVHD.
AB - Delayed platelet recovery (DPR) despite prompt neutrophil engraftment is frequently observed after allogeneic hematopoietic stem cell transplantation (HSCT). However, few studies have evaluated the risk factors and long-term outcome. Therefore, we retrospectively analysed 219 adult patients who underwent their first allogenic HSCT with neutrophil engraftment. Of these 219 patients, 50 (22.8%) had DPR that was defined as relapse-free survival at day 60 after HSCT without primary platelet recovery despite neutrophil engraftment. The results of a multivariate analysis showed that a high-risk underlying disease (odds ratio [OR], 2.38; 95% confidence interval [CI], 1.04-5.48; P =.041) and human leukocyte antigen–mismatched HSCT (OR, 2.63; 95% CI, 1.28-5.43; P =.009) were associated with an increased risk of DPR. In univariate analyses, the occurrence of DPR was significantly associated with inferior overall survival, high nonrelapse mortality, and a low incidence of chronic graft-versus-host disease (GVHD), despite a comparable relapse rate. In multivariate analyses, DPR was associated with inferior overall survival (hazard ratio [HR], 2.00; 95% CI, 1.23-3.27; P =.005) and a low incidence of chronic GVHD (HR, 0.42; 95% CI, 0.22-0.78; P =.002). In conclusion, DPR was a strong predictor of shorter survival but also less frequent chronic GVHD.
KW - allogenic hematopoietic stem cell transplantation
KW - chronic graft-versus-host disease
KW - platelet engraftment
KW - stem cell source
KW - thrombocytopenia
UR - https://www.scopus.com/pages/publications/85018396935
U2 - 10.1002/hon.2427
DO - 10.1002/hon.2427
M3 - Article
C2 - 28474740
AN - SCOPUS:85018396935
SN - 0278-0232
VL - 36
SP - 276
EP - 284
JO - Hematological Oncology
JF - Hematological Oncology
IS - 1
ER -