Cargando…
Stem cell transplant for mantle cell lymphoma in Taiwan
Mantle cell lymphoma (MCL) is a B-cell lymphoma featuring an aggressive course and a progressive relapsing pattern. International guidelines recommend early consolidative autologous stem cell transplant (auto-SCT) for eligible patients while reserving allogeneic SCT (allo-SCT) as therapy for refract...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8983774/ https://www.ncbi.nlm.nih.gov/pubmed/35383213 http://dx.doi.org/10.1038/s41598-022-09539-5 |
_version_ | 1784682032005120000 |
---|---|
author | Wang, Yu-Hung Hsieh, Ching-Yun Hsiao, Liang-Tsai Lin, Tung-Liang Liu, Yi-Chang Yao, Ming Tan, Tran-Der Ko, Bor-Sheng |
author_facet | Wang, Yu-Hung Hsieh, Ching-Yun Hsiao, Liang-Tsai Lin, Tung-Liang Liu, Yi-Chang Yao, Ming Tan, Tran-Der Ko, Bor-Sheng |
author_sort | Wang, Yu-Hung |
collection | PubMed |
description | Mantle cell lymphoma (MCL) is a B-cell lymphoma featuring an aggressive course and a progressive relapsing pattern. International guidelines recommend early consolidative autologous stem cell transplant (auto-SCT) for eligible patients while reserving allogeneic SCT (allo-SCT) as therapy for refractory cases. Since data describing the implementation of transplants in the Asian population with MCL are limited, we aimed to analyze post-SCT outcomes of 99 MCL patients from the Taiwan Bone Marrow Transplant Registry database. The median age was 56 years, and 11% of the patients had blastoid variant MCL. Ninety-four patients received auto-SCT, while 13 patients received allo-SCT, eight of which received allo-SCT after failing auto-SCT. Before auto-SCT, 52% of the patients were in their first complete remission (CR1). Overall, 37 patients (39%) relapsed after auto-SCT. The median post-auto-SCT progression-free survival and overall survival (OS) were 43.6 months and not reached, respectively. Blastoid variant MCL, transplant not received in CR1, and disease progression within 12 months post-auto-SCT independently predicted inferior OS in multivariable analysis. The median post-allo-SCT OS was 74 months. Two patients (15%) died of MCL recurrence post-allo-SCT. Three patients with refractory diseases were salvaged with ibrutinib or venetoclax to allo-SCT. Treatment strategies incorporating novel agents warrant further optimization. |
format | Online Article Text |
id | pubmed-8983774 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-89837742022-04-06 Stem cell transplant for mantle cell lymphoma in Taiwan Wang, Yu-Hung Hsieh, Ching-Yun Hsiao, Liang-Tsai Lin, Tung-Liang Liu, Yi-Chang Yao, Ming Tan, Tran-Der Ko, Bor-Sheng Sci Rep Article Mantle cell lymphoma (MCL) is a B-cell lymphoma featuring an aggressive course and a progressive relapsing pattern. International guidelines recommend early consolidative autologous stem cell transplant (auto-SCT) for eligible patients while reserving allogeneic SCT (allo-SCT) as therapy for refractory cases. Since data describing the implementation of transplants in the Asian population with MCL are limited, we aimed to analyze post-SCT outcomes of 99 MCL patients from the Taiwan Bone Marrow Transplant Registry database. The median age was 56 years, and 11% of the patients had blastoid variant MCL. Ninety-four patients received auto-SCT, while 13 patients received allo-SCT, eight of which received allo-SCT after failing auto-SCT. Before auto-SCT, 52% of the patients were in their first complete remission (CR1). Overall, 37 patients (39%) relapsed after auto-SCT. The median post-auto-SCT progression-free survival and overall survival (OS) were 43.6 months and not reached, respectively. Blastoid variant MCL, transplant not received in CR1, and disease progression within 12 months post-auto-SCT independently predicted inferior OS in multivariable analysis. The median post-allo-SCT OS was 74 months. Two patients (15%) died of MCL recurrence post-allo-SCT. Three patients with refractory diseases were salvaged with ibrutinib or venetoclax to allo-SCT. Treatment strategies incorporating novel agents warrant further optimization. Nature Publishing Group UK 2022-04-05 /pmc/articles/PMC8983774/ /pubmed/35383213 http://dx.doi.org/10.1038/s41598-022-09539-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Wang, Yu-Hung Hsieh, Ching-Yun Hsiao, Liang-Tsai Lin, Tung-Liang Liu, Yi-Chang Yao, Ming Tan, Tran-Der Ko, Bor-Sheng Stem cell transplant for mantle cell lymphoma in Taiwan |
title | Stem cell transplant for mantle cell lymphoma in Taiwan |
title_full | Stem cell transplant for mantle cell lymphoma in Taiwan |
title_fullStr | Stem cell transplant for mantle cell lymphoma in Taiwan |
title_full_unstemmed | Stem cell transplant for mantle cell lymphoma in Taiwan |
title_short | Stem cell transplant for mantle cell lymphoma in Taiwan |
title_sort | stem cell transplant for mantle cell lymphoma in taiwan |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8983774/ https://www.ncbi.nlm.nih.gov/pubmed/35383213 http://dx.doi.org/10.1038/s41598-022-09539-5 |
work_keys_str_mv | AT wangyuhung stemcelltransplantformantlecelllymphomaintaiwan AT hsiehchingyun stemcelltransplantformantlecelllymphomaintaiwan AT hsiaoliangtsai stemcelltransplantformantlecelllymphomaintaiwan AT lintungliang stemcelltransplantformantlecelllymphomaintaiwan AT liuyichang stemcelltransplantformantlecelllymphomaintaiwan AT yaoming stemcelltransplantformantlecelllymphomaintaiwan AT tantrander stemcelltransplantformantlecelllymphomaintaiwan AT koborsheng stemcelltransplantformantlecelllymphomaintaiwan |