Modified conditioning regimen with idarubicin followed by autologous hematopoietic stem cell transplantation for invasive B-cell non-Hodgkin’s lymphoma patients

Abstract High-dose chemotherapy followed by autologous hematopoietic stem cell transplantation (ASCT) is still a consolidation treatment choice for relapsed/refractory B-cell non-Hodgkin’s lymphoma (NHL) patients and some aggressive B-cell NHL as frontline therapy. Due to the shortage of carmustine,...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Chen Tian, Yueyang Li, Su Liu, Zehui Chen, Yizhuo Zhang, Yong Yu, Hongliang Yang, Haifeng Zhao, Zhigang Zhao, Tian Yuan, Yafei Wang
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2021
Materias:
R
Q
Acceso en línea:https://doaj.org/article/c16017e1730f4917868c441896b63577
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:c16017e1730f4917868c441896b63577
record_format dspace
spelling oai:doaj.org-article:c16017e1730f4917868c441896b635772021-12-02T12:11:52ZModified conditioning regimen with idarubicin followed by autologous hematopoietic stem cell transplantation for invasive B-cell non-Hodgkin’s lymphoma patients10.1038/s41598-021-81944-82045-2322https://doaj.org/article/c16017e1730f4917868c441896b635772021-02-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-81944-8https://doaj.org/toc/2045-2322Abstract High-dose chemotherapy followed by autologous hematopoietic stem cell transplantation (ASCT) is still a consolidation treatment choice for relapsed/refractory B-cell non-Hodgkin’s lymphoma (NHL) patients and some aggressive B-cell NHL as frontline therapy. Due to the shortage of carmustine, we switched to idarubicin-substituted BEAC (IEAC) conditioning regimen. We retrospectively compared the outcomes of 72 aggressive B-cell NHL patients treated with IEAC or BEAC regimens followed by ASCT as upfront consolidative treatment. The median time to neutrophil and platelet reconstitution showed no difference between IEAC and BEAC groups. IEAC regimen was well tolerated without increase of adverse events. Transplant-related mortality didn’t occur. The overall survival (OS) and progression-free survival (PFS) of IEAC group (33 and 23 months) were a little longer than that of BEAC group (30 and 18 months). However, due to the small sample numbers, there’s no significant difference in OS and PFS between IEAC and BEAC group with DLBCL or MCL. Multivariate analysis showed that AnnArbor staging, IPI score, lactate dehydrogenase level, remission of disease, modified regimen were related with PFS and OS. In conclusion, IEAC regimen was well tolerated and replacement with idarubicin could be an alternative when carmustine was not available.Chen TianYueyang LiSu LiuZehui ChenYizhuo ZhangYong YuHongliang YangHaifeng ZhaoZhigang ZhaoTian YuanYafei WangNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-8 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Chen Tian
Yueyang Li
Su Liu
Zehui Chen
Yizhuo Zhang
Yong Yu
Hongliang Yang
Haifeng Zhao
Zhigang Zhao
Tian Yuan
Yafei Wang
Modified conditioning regimen with idarubicin followed by autologous hematopoietic stem cell transplantation for invasive B-cell non-Hodgkin’s lymphoma patients
description Abstract High-dose chemotherapy followed by autologous hematopoietic stem cell transplantation (ASCT) is still a consolidation treatment choice for relapsed/refractory B-cell non-Hodgkin’s lymphoma (NHL) patients and some aggressive B-cell NHL as frontline therapy. Due to the shortage of carmustine, we switched to idarubicin-substituted BEAC (IEAC) conditioning regimen. We retrospectively compared the outcomes of 72 aggressive B-cell NHL patients treated with IEAC or BEAC regimens followed by ASCT as upfront consolidative treatment. The median time to neutrophil and platelet reconstitution showed no difference between IEAC and BEAC groups. IEAC regimen was well tolerated without increase of adverse events. Transplant-related mortality didn’t occur. The overall survival (OS) and progression-free survival (PFS) of IEAC group (33 and 23 months) were a little longer than that of BEAC group (30 and 18 months). However, due to the small sample numbers, there’s no significant difference in OS and PFS between IEAC and BEAC group with DLBCL or MCL. Multivariate analysis showed that AnnArbor staging, IPI score, lactate dehydrogenase level, remission of disease, modified regimen were related with PFS and OS. In conclusion, IEAC regimen was well tolerated and replacement with idarubicin could be an alternative when carmustine was not available.
format article
author Chen Tian
Yueyang Li
Su Liu
Zehui Chen
Yizhuo Zhang
Yong Yu
Hongliang Yang
Haifeng Zhao
Zhigang Zhao
Tian Yuan
Yafei Wang
author_facet Chen Tian
Yueyang Li
Su Liu
Zehui Chen
Yizhuo Zhang
Yong Yu
Hongliang Yang
Haifeng Zhao
Zhigang Zhao
Tian Yuan
Yafei Wang
author_sort Chen Tian
title Modified conditioning regimen with idarubicin followed by autologous hematopoietic stem cell transplantation for invasive B-cell non-Hodgkin’s lymphoma patients
title_short Modified conditioning regimen with idarubicin followed by autologous hematopoietic stem cell transplantation for invasive B-cell non-Hodgkin’s lymphoma patients
title_full Modified conditioning regimen with idarubicin followed by autologous hematopoietic stem cell transplantation for invasive B-cell non-Hodgkin’s lymphoma patients
title_fullStr Modified conditioning regimen with idarubicin followed by autologous hematopoietic stem cell transplantation for invasive B-cell non-Hodgkin’s lymphoma patients
title_full_unstemmed Modified conditioning regimen with idarubicin followed by autologous hematopoietic stem cell transplantation for invasive B-cell non-Hodgkin’s lymphoma patients
title_sort modified conditioning regimen with idarubicin followed by autologous hematopoietic stem cell transplantation for invasive b-cell non-hodgkin’s lymphoma patients
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/c16017e1730f4917868c441896b63577
work_keys_str_mv AT chentian modifiedconditioningregimenwithidarubicinfollowedbyautologoushematopoieticstemcelltransplantationforinvasivebcellnonhodgkinslymphomapatients
AT yueyangli modifiedconditioningregimenwithidarubicinfollowedbyautologoushematopoieticstemcelltransplantationforinvasivebcellnonhodgkinslymphomapatients
AT suliu modifiedconditioningregimenwithidarubicinfollowedbyautologoushematopoieticstemcelltransplantationforinvasivebcellnonhodgkinslymphomapatients
AT zehuichen modifiedconditioningregimenwithidarubicinfollowedbyautologoushematopoieticstemcelltransplantationforinvasivebcellnonhodgkinslymphomapatients
AT yizhuozhang modifiedconditioningregimenwithidarubicinfollowedbyautologoushematopoieticstemcelltransplantationforinvasivebcellnonhodgkinslymphomapatients
AT yongyu modifiedconditioningregimenwithidarubicinfollowedbyautologoushematopoieticstemcelltransplantationforinvasivebcellnonhodgkinslymphomapatients
AT hongliangyang modifiedconditioningregimenwithidarubicinfollowedbyautologoushematopoieticstemcelltransplantationforinvasivebcellnonhodgkinslymphomapatients
AT haifengzhao modifiedconditioningregimenwithidarubicinfollowedbyautologoushematopoieticstemcelltransplantationforinvasivebcellnonhodgkinslymphomapatients
AT zhigangzhao modifiedconditioningregimenwithidarubicinfollowedbyautologoushematopoieticstemcelltransplantationforinvasivebcellnonhodgkinslymphomapatients
AT tianyuan modifiedconditioningregimenwithidarubicinfollowedbyautologoushematopoieticstemcelltransplantationforinvasivebcellnonhodgkinslymphomapatients
AT yafeiwang modifiedconditioningregimenwithidarubicinfollowedbyautologoushematopoieticstemcelltransplantationforinvasivebcellnonhodgkinslymphomapatients
_version_ 1718394597794643968