Haploidentical donor transplant is associated with secondary poor graft function after allogeneic stem cell transplantation: A single‐center retrospective study

Abstract Background Secondary poor graft function (sPGF) is a serious complication after allogeneic hematopoietic stem cell transplantation (allo‐HSCT) related to poor outcome. We aimed to retrospectively evaluate the morbidity and hazard elements of sPGF after allo‐HSCT. Methods Eight hundred and s...

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Autores principales: Wei‐Ran Lv, Ya Zhou, Jun Xu, Zhi‐Ping Fan, Fen Huang, Na Xu, Li Xuan, Peng‐Cheng Shi, Hui Liu, Zhi‐Xiang Wang, Jing Sun, Qi‐Fa Liu
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Publicado: Wiley 2021
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spelling oai:doaj.org-article:5476aeff76f8453bb3b98e200d363d322021-12-01T04:49:15ZHaploidentical donor transplant is associated with secondary poor graft function after allogeneic stem cell transplantation: A single‐center retrospective study2045-763410.1002/cam4.4353https://doaj.org/article/5476aeff76f8453bb3b98e200d363d322021-12-01T00:00:00Zhttps://doi.org/10.1002/cam4.4353https://doaj.org/toc/2045-7634Abstract Background Secondary poor graft function (sPGF) is a serious complication after allogeneic hematopoietic stem cell transplantation (allo‐HSCT) related to poor outcome. We aimed to retrospectively evaluate the morbidity and hazard elements of sPGF after allo‐HSCT. Methods Eight hundred and sixty‐three patients who achieved initial engraftment of both neutrophils and platelets were retrospectively reviewed in this study. Results Fifty‐two patients developed sPGF within 180 days post‐transplants, with the median onset time was 62 days (range, 34–121 days) post‐transplants. The overall cumulative incidence of sPGF within 180 days post‐transplantation was 6.0%, with 3.4%, 3.4%, and 10.1%, respectively, in matched sibling donor (MSD), matched unrelated donor (MUD), and haploidentical donor (HID) transplant (p < 0.0001). Multivariable analysis showed that HID (HID vs. MSD: hazard ratio [HR] 2.525, p = 0.004; HID vs. MUD: [HR] 3.531, p = 0.017), acute graft versus host disease (aGVHD) within +30 days ([HR] 2.323, p = 0.003), and cytomegalovirus (CMV) reactivation ([HR] 8.915, p < 0.0001) within +30 days post‐transplants were hazard elements of sPGF. The patients with sPGF had poorer survival than good graft function (51.7±8.1% vs. 62.9±1.9%, p < 0.0001). Our results also showed that only CMV reactivation was the hazard element for the development of PGF in HID transplant ([HR] 12.521 p < 0.0001). Conclusion HID transplant is also an independent hazard element of sPGF except for aGVHD and CMV reactivation.Wei‐Ran LvYa ZhouJun XuZhi‐Ping FanFen HuangNa XuLi XuanPeng‐Cheng ShiHui LiuZhi‐Xiang WangJing SunQi‐Fa LiuWileyarticlehaploidentical donor transplanthazard elementshematopoietic stem cell transplantationsecondary poor graft functionNeoplasms. Tumors. Oncology. Including cancer and carcinogensRC254-282ENCancer Medicine, Vol 10, Iss 23, Pp 8497-8506 (2021)
institution DOAJ
collection DOAJ
language EN
topic haploidentical donor transplant
hazard elements
hematopoietic stem cell transplantation
secondary poor graft function
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
spellingShingle haploidentical donor transplant
hazard elements
hematopoietic stem cell transplantation
secondary poor graft function
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
Wei‐Ran Lv
Ya Zhou
Jun Xu
Zhi‐Ping Fan
Fen Huang
Na Xu
Li Xuan
Peng‐Cheng Shi
Hui Liu
Zhi‐Xiang Wang
Jing Sun
Qi‐Fa Liu
Haploidentical donor transplant is associated with secondary poor graft function after allogeneic stem cell transplantation: A single‐center retrospective study
description Abstract Background Secondary poor graft function (sPGF) is a serious complication after allogeneic hematopoietic stem cell transplantation (allo‐HSCT) related to poor outcome. We aimed to retrospectively evaluate the morbidity and hazard elements of sPGF after allo‐HSCT. Methods Eight hundred and sixty‐three patients who achieved initial engraftment of both neutrophils and platelets were retrospectively reviewed in this study. Results Fifty‐two patients developed sPGF within 180 days post‐transplants, with the median onset time was 62 days (range, 34–121 days) post‐transplants. The overall cumulative incidence of sPGF within 180 days post‐transplantation was 6.0%, with 3.4%, 3.4%, and 10.1%, respectively, in matched sibling donor (MSD), matched unrelated donor (MUD), and haploidentical donor (HID) transplant (p < 0.0001). Multivariable analysis showed that HID (HID vs. MSD: hazard ratio [HR] 2.525, p = 0.004; HID vs. MUD: [HR] 3.531, p = 0.017), acute graft versus host disease (aGVHD) within +30 days ([HR] 2.323, p = 0.003), and cytomegalovirus (CMV) reactivation ([HR] 8.915, p < 0.0001) within +30 days post‐transplants were hazard elements of sPGF. The patients with sPGF had poorer survival than good graft function (51.7±8.1% vs. 62.9±1.9%, p < 0.0001). Our results also showed that only CMV reactivation was the hazard element for the development of PGF in HID transplant ([HR] 12.521 p < 0.0001). Conclusion HID transplant is also an independent hazard element of sPGF except for aGVHD and CMV reactivation.
format article
author Wei‐Ran Lv
Ya Zhou
Jun Xu
Zhi‐Ping Fan
Fen Huang
Na Xu
Li Xuan
Peng‐Cheng Shi
Hui Liu
Zhi‐Xiang Wang
Jing Sun
Qi‐Fa Liu
author_facet Wei‐Ran Lv
Ya Zhou
Jun Xu
Zhi‐Ping Fan
Fen Huang
Na Xu
Li Xuan
Peng‐Cheng Shi
Hui Liu
Zhi‐Xiang Wang
Jing Sun
Qi‐Fa Liu
author_sort Wei‐Ran Lv
title Haploidentical donor transplant is associated with secondary poor graft function after allogeneic stem cell transplantation: A single‐center retrospective study
title_short Haploidentical donor transplant is associated with secondary poor graft function after allogeneic stem cell transplantation: A single‐center retrospective study
title_full Haploidentical donor transplant is associated with secondary poor graft function after allogeneic stem cell transplantation: A single‐center retrospective study
title_fullStr Haploidentical donor transplant is associated with secondary poor graft function after allogeneic stem cell transplantation: A single‐center retrospective study
title_full_unstemmed Haploidentical donor transplant is associated with secondary poor graft function after allogeneic stem cell transplantation: A single‐center retrospective study
title_sort haploidentical donor transplant is associated with secondary poor graft function after allogeneic stem cell transplantation: a single‐center retrospective study
publisher Wiley
publishDate 2021
url https://doaj.org/article/5476aeff76f8453bb3b98e200d363d32
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