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...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Yu-Hung, Hsieh, Ching-Yun, Hsiao, Liang-Tsai, Lin, Tung-Liang, Liu, Yi-Chang, Yao, Ming, Tan, Tran-Der, Ko, Bor-Sheng
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