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T Cell-Replete Haploidentical Peripheral Blood Hematopoietic Cell Transplantation for Treatment of T-Lymphoblastic Lymphoma
BACKGROUND: There is currently little information on haploidentical hematopoietic cell transplantation (haplo-HCT) for T-lymphoblastic lymphoma (T-LBL). Data about peripheral blood stem cells (PBSC) as a reliable graft source for T-LBL treatment are lacking. MATERIAL/METHODS: T-LBL patients who unde...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Scientific Literature, Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6248294/ https://www.ncbi.nlm.nih.gov/pubmed/29930241 http://dx.doi.org/10.12659/AOT.909122 |
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author | Guan, Lixun Li, Xiaohong Wei, Huaping Gu, Zhenyang Zhao, Shasha Zhu, Chengying Yang, Nan Wang, Feiyan Luo, Lan Gao, Zhe Huang, Wenrong Li, Honghua Wang, Quanshun Liu, Daihong Wu, Xiaoxiong Gao, Chunji |
author_facet | Guan, Lixun Li, Xiaohong Wei, Huaping Gu, Zhenyang Zhao, Shasha Zhu, Chengying Yang, Nan Wang, Feiyan Luo, Lan Gao, Zhe Huang, Wenrong Li, Honghua Wang, Quanshun Liu, Daihong Wu, Xiaoxiong Gao, Chunji |
author_sort | Guan, Lixun |
collection | PubMed |
description | BACKGROUND: There is currently little information on haploidentical hematopoietic cell transplantation (haplo-HCT) for T-lymphoblastic lymphoma (T-LBL). Data about peripheral blood stem cells (PBSC) as a reliable graft source for T-LBL treatment are lacking. MATERIAL/METHODS: T-LBL patients who underwent T cell-replete haploidentical peripheral blood hematopoietic cell transplantation (haplo-PBHCT) from July 2007 to January 2017 were retrospectively evaluated. RESULTS: A total of 25 patients (age ≥15 years) with median age of 24 (range 15–51) years were enrolled. The median number of CD34+ cells infused was 5.0 (1.6–14.4) 10(6)/kg. Sustained myeloid engraftment with full donor chimerism was achieved in all patients. The cumulative incidence of grades 2 to 4 acute graft-versus-host disease (GVHD) at day 100 was 24%. Two-year extensive chronic GVHD cumulative incidence was 20%. The 3-year overall survival rate for all patients was 70%. The median survival time of the complete remission (CR) group was better than that of the non-CR group (not reached vs. 9 m) (P<0.01). The relapse rate was 17% for patients who obtained CR and were given haplo-HCT as consolidation treatment. CONCLUSIONS: This study indicates that haplo-PBHCT is a safe and effective method for the treatment of T-LBL. |
format | Online Article Text |
id | pubmed-6248294 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | International Scientific Literature, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-62482942018-11-28 T Cell-Replete Haploidentical Peripheral Blood Hematopoietic Cell Transplantation for Treatment of T-Lymphoblastic Lymphoma Guan, Lixun Li, Xiaohong Wei, Huaping Gu, Zhenyang Zhao, Shasha Zhu, Chengying Yang, Nan Wang, Feiyan Luo, Lan Gao, Zhe Huang, Wenrong Li, Honghua Wang, Quanshun Liu, Daihong Wu, Xiaoxiong Gao, Chunji Ann Transplant Original Paper BACKGROUND: There is currently little information on haploidentical hematopoietic cell transplantation (haplo-HCT) for T-lymphoblastic lymphoma (T-LBL). Data about peripheral blood stem cells (PBSC) as a reliable graft source for T-LBL treatment are lacking. MATERIAL/METHODS: T-LBL patients who underwent T cell-replete haploidentical peripheral blood hematopoietic cell transplantation (haplo-PBHCT) from July 2007 to January 2017 were retrospectively evaluated. RESULTS: A total of 25 patients (age ≥15 years) with median age of 24 (range 15–51) years were enrolled. The median number of CD34+ cells infused was 5.0 (1.6–14.4) 10(6)/kg. Sustained myeloid engraftment with full donor chimerism was achieved in all patients. The cumulative incidence of grades 2 to 4 acute graft-versus-host disease (GVHD) at day 100 was 24%. Two-year extensive chronic GVHD cumulative incidence was 20%. The 3-year overall survival rate for all patients was 70%. The median survival time of the complete remission (CR) group was better than that of the non-CR group (not reached vs. 9 m) (P<0.01). The relapse rate was 17% for patients who obtained CR and were given haplo-HCT as consolidation treatment. CONCLUSIONS: This study indicates that haplo-PBHCT is a safe and effective method for the treatment of T-LBL. International Scientific Literature, Inc. 2018-06-22 /pmc/articles/PMC6248294/ /pubmed/29930241 http://dx.doi.org/10.12659/AOT.909122 Text en © Ann Transplant, 2018 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) ) |
spellingShingle | Original Paper Guan, Lixun Li, Xiaohong Wei, Huaping Gu, Zhenyang Zhao, Shasha Zhu, Chengying Yang, Nan Wang, Feiyan Luo, Lan Gao, Zhe Huang, Wenrong Li, Honghua Wang, Quanshun Liu, Daihong Wu, Xiaoxiong Gao, Chunji T Cell-Replete Haploidentical Peripheral Blood Hematopoietic Cell Transplantation for Treatment of T-Lymphoblastic Lymphoma |
title | T Cell-Replete Haploidentical Peripheral Blood Hematopoietic Cell Transplantation for Treatment of T-Lymphoblastic Lymphoma |
title_full | T Cell-Replete Haploidentical Peripheral Blood Hematopoietic Cell Transplantation for Treatment of T-Lymphoblastic Lymphoma |
title_fullStr | T Cell-Replete Haploidentical Peripheral Blood Hematopoietic Cell Transplantation for Treatment of T-Lymphoblastic Lymphoma |
title_full_unstemmed | T Cell-Replete Haploidentical Peripheral Blood Hematopoietic Cell Transplantation for Treatment of T-Lymphoblastic Lymphoma |
title_short | T Cell-Replete Haploidentical Peripheral Blood Hematopoietic Cell Transplantation for Treatment of T-Lymphoblastic Lymphoma |
title_sort | t cell-replete haploidentical peripheral blood hematopoietic cell transplantation for treatment of t-lymphoblastic lymphoma |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6248294/ https://www.ncbi.nlm.nih.gov/pubmed/29930241 http://dx.doi.org/10.12659/AOT.909122 |
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