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Tumorablative conditioning regimen for haploidentical stem cell transplantation in 102 children with hematologic malignancies: a single-center experience

Haploidentical hematopoietic stem cell transplantation (Haplo-HSCT) is widely carried out in China, and transplantation related complications decreased gradually with the transplant technology improving, and the overall survival(OS) increased year by year. However, relapse after transplantation is s...

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Autores principales: Rongmu, Luo, Xiaomei, Zhang, Zhenlan, Du, Ya, Wang, Wei, Chen, Yingjian, Si, Wenjing, Gu, Guosheng, Xing, Yang, Wang, Wanming, Da
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5768360/
https://www.ncbi.nlm.nih.gov/pubmed/29371943
http://dx.doi.org/10.18632/oncotarget.22893
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author Rongmu, Luo
Xiaomei, Zhang
Zhenlan, Du
Ya, Wang
Wei, Chen
Yingjian, Si
Wenjing, Gu
Guosheng, Xing
Yang, Wang
Wanming, Da
author_facet Rongmu, Luo
Xiaomei, Zhang
Zhenlan, Du
Ya, Wang
Wei, Chen
Yingjian, Si
Wenjing, Gu
Guosheng, Xing
Yang, Wang
Wanming, Da
author_sort Rongmu, Luo
collection PubMed
description Haploidentical hematopoietic stem cell transplantation (Haplo-HSCT) is widely carried out in China, and transplantation related complications decreased gradually with the transplant technology improving, and the overall survival(OS) increased year by year. However, relapse after transplantation is still one of the main causes of death in patients with hematological malignancy. In order to reduce the recurrence after HSCT, we set a tumorablative conditioning regimen (TAC ) regimen; the aim is as much as possible to eliminate the malignant clone to reduce the recurrence without increasing the conditioning toxicity. We retrospectively analyzed 102 cases of haplo-HSCT in our hospital from 2012 to 2017. Ninety-eight out of the 99 (99.0%) patients achieved primary engraftment. The 2-year OS and disease free survival (DFS) are 81.4% (83/102) and 77.45% (79/102). The cumulative incidence of leukemia relapse is 16.2% (16/99), Twenty-nine patients developed II-IV acute graft-versus-host disease (aGVHD) (29%) within 100 days and only nine patients have grade III-IV aGVHD (9%) in measurable 99 patients. The conditioning regimen was relatively well tolerated with limited regimen-related toxicity. The preliminary results show that TAC is safe and effective in haplo-HSCT of children with hematologic malignancies. This study will provide a clinical basis for the individualized conditioning regimen.
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spelling pubmed-57683602018-01-25 Tumorablative conditioning regimen for haploidentical stem cell transplantation in 102 children with hematologic malignancies: a single-center experience Rongmu, Luo Xiaomei, Zhang Zhenlan, Du Ya, Wang Wei, Chen Yingjian, Si Wenjing, Gu Guosheng, Xing Yang, Wang Wanming, Da Oncotarget Research Paper Haploidentical hematopoietic stem cell transplantation (Haplo-HSCT) is widely carried out in China, and transplantation related complications decreased gradually with the transplant technology improving, and the overall survival(OS) increased year by year. However, relapse after transplantation is still one of the main causes of death in patients with hematological malignancy. In order to reduce the recurrence after HSCT, we set a tumorablative conditioning regimen (TAC ) regimen; the aim is as much as possible to eliminate the malignant clone to reduce the recurrence without increasing the conditioning toxicity. We retrospectively analyzed 102 cases of haplo-HSCT in our hospital from 2012 to 2017. Ninety-eight out of the 99 (99.0%) patients achieved primary engraftment. The 2-year OS and disease free survival (DFS) are 81.4% (83/102) and 77.45% (79/102). The cumulative incidence of leukemia relapse is 16.2% (16/99), Twenty-nine patients developed II-IV acute graft-versus-host disease (aGVHD) (29%) within 100 days and only nine patients have grade III-IV aGVHD (9%) in measurable 99 patients. The conditioning regimen was relatively well tolerated with limited regimen-related toxicity. The preliminary results show that TAC is safe and effective in haplo-HSCT of children with hematologic malignancies. This study will provide a clinical basis for the individualized conditioning regimen. Impact Journals LLC 2017-12-04 /pmc/articles/PMC5768360/ /pubmed/29371943 http://dx.doi.org/10.18632/oncotarget.22893 Text en Copyright: © 2017 Rongmu et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Rongmu, Luo
Xiaomei, Zhang
Zhenlan, Du
Ya, Wang
Wei, Chen
Yingjian, Si
Wenjing, Gu
Guosheng, Xing
Yang, Wang
Wanming, Da
Tumorablative conditioning regimen for haploidentical stem cell transplantation in 102 children with hematologic malignancies: a single-center experience
title Tumorablative conditioning regimen for haploidentical stem cell transplantation in 102 children with hematologic malignancies: a single-center experience
title_full Tumorablative conditioning regimen for haploidentical stem cell transplantation in 102 children with hematologic malignancies: a single-center experience
title_fullStr Tumorablative conditioning regimen for haploidentical stem cell transplantation in 102 children with hematologic malignancies: a single-center experience
title_full_unstemmed Tumorablative conditioning regimen for haploidentical stem cell transplantation in 102 children with hematologic malignancies: a single-center experience
title_short Tumorablative conditioning regimen for haploidentical stem cell transplantation in 102 children with hematologic malignancies: a single-center experience
title_sort tumorablative conditioning regimen for haploidentical stem cell transplantation in 102 children with hematologic malignancies: a single-center experience
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5768360/
https://www.ncbi.nlm.nih.gov/pubmed/29371943
http://dx.doi.org/10.18632/oncotarget.22893
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