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Bortezomib-based therapy for transplant-ineligible East Asian patients with newly diagnosed mantle-cell lymphoma

INTRODUCTION: This subgroup analysis of the LYM-3002 Phase III study (NCT00722137) investigated whether substituting bortezomib for vincristine in frontline R-CHOP (rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone) therapy could improve outcomes in East Asian patients with n...

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Autores principales: Jin, Jie, Okamoto, Rumiko, Yoon, Sung-Soo, Shih, Lee-Yung, Zhu, Jun, Liu, Ting, Hong, Xiaonan, Pei, Lixia, Rooney, Brendan, van de Velde, Helgi, Huang, Huiqiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6039072/
https://www.ncbi.nlm.nih.gov/pubmed/30013367
http://dx.doi.org/10.2147/OTT.S150339
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author Jin, Jie
Okamoto, Rumiko
Yoon, Sung-Soo
Shih, Lee-Yung
Zhu, Jun
Liu, Ting
Hong, Xiaonan
Pei, Lixia
Rooney, Brendan
van de Velde, Helgi
Huang, Huiqiang
author_facet Jin, Jie
Okamoto, Rumiko
Yoon, Sung-Soo
Shih, Lee-Yung
Zhu, Jun
Liu, Ting
Hong, Xiaonan
Pei, Lixia
Rooney, Brendan
van de Velde, Helgi
Huang, Huiqiang
author_sort Jin, Jie
collection PubMed
description INTRODUCTION: This subgroup analysis of the LYM-3002 Phase III study (NCT00722137) investigated whether substituting bortezomib for vincristine in frontline R-CHOP (rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone) therapy could improve outcomes in East Asian patients with newly diagnosed mantle-cell lymphoma (MCL). MATERIALS AND METHODS: A total of 121 East Asian patients from China, Taiwan, Japan, and the Republic of Korea with stage II–IV MCL who were ineligible or not considered for stem-cell transplantation were enrolled to six to eight 21-day cycles of R-CHOP or VR-CAP (R-CHOP with bortezomib replacing vincristine). RESULTS: The primary end point was progression-free survival. After a median follow-up of 42.4 months, median progression-free survival in East Asian patients was 13.9 (R-CHOP) versus 28.6 (VR-CAP) months (HR 0.7, P=0.157; 43% improvement with VR-CAP). Secondary end points (R-CHOP vs VR-CAP), including complete response rate (47% vs 63%), duration of complete response (median 16.6 vs 46.7 months), and treatment-free interval (median 21 vs 46.5 months), were improved with VR-CAP. VR-CAP was associated with increased but manageable toxicity. The most frequent adverse events were hematologic toxicities. CONCLUSION: VR-CAP was effective in East Asian patients with newly diagnosed MCL, and could be considered for patients in whom stem-cell transplantation is not an option.
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spelling pubmed-60390722018-07-16 Bortezomib-based therapy for transplant-ineligible East Asian patients with newly diagnosed mantle-cell lymphoma Jin, Jie Okamoto, Rumiko Yoon, Sung-Soo Shih, Lee-Yung Zhu, Jun Liu, Ting Hong, Xiaonan Pei, Lixia Rooney, Brendan van de Velde, Helgi Huang, Huiqiang Onco Targets Ther Original Research INTRODUCTION: This subgroup analysis of the LYM-3002 Phase III study (NCT00722137) investigated whether substituting bortezomib for vincristine in frontline R-CHOP (rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone) therapy could improve outcomes in East Asian patients with newly diagnosed mantle-cell lymphoma (MCL). MATERIALS AND METHODS: A total of 121 East Asian patients from China, Taiwan, Japan, and the Republic of Korea with stage II–IV MCL who were ineligible or not considered for stem-cell transplantation were enrolled to six to eight 21-day cycles of R-CHOP or VR-CAP (R-CHOP with bortezomib replacing vincristine). RESULTS: The primary end point was progression-free survival. After a median follow-up of 42.4 months, median progression-free survival in East Asian patients was 13.9 (R-CHOP) versus 28.6 (VR-CAP) months (HR 0.7, P=0.157; 43% improvement with VR-CAP). Secondary end points (R-CHOP vs VR-CAP), including complete response rate (47% vs 63%), duration of complete response (median 16.6 vs 46.7 months), and treatment-free interval (median 21 vs 46.5 months), were improved with VR-CAP. VR-CAP was associated with increased but manageable toxicity. The most frequent adverse events were hematologic toxicities. CONCLUSION: VR-CAP was effective in East Asian patients with newly diagnosed MCL, and could be considered for patients in whom stem-cell transplantation is not an option. Dove Medical Press 2018-07-06 /pmc/articles/PMC6039072/ /pubmed/30013367 http://dx.doi.org/10.2147/OTT.S150339 Text en © 2018 Jin et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Jin, Jie
Okamoto, Rumiko
Yoon, Sung-Soo
Shih, Lee-Yung
Zhu, Jun
Liu, Ting
Hong, Xiaonan
Pei, Lixia
Rooney, Brendan
van de Velde, Helgi
Huang, Huiqiang
Bortezomib-based therapy for transplant-ineligible East Asian patients with newly diagnosed mantle-cell lymphoma
title Bortezomib-based therapy for transplant-ineligible East Asian patients with newly diagnosed mantle-cell lymphoma
title_full Bortezomib-based therapy for transplant-ineligible East Asian patients with newly diagnosed mantle-cell lymphoma
title_fullStr Bortezomib-based therapy for transplant-ineligible East Asian patients with newly diagnosed mantle-cell lymphoma
title_full_unstemmed Bortezomib-based therapy for transplant-ineligible East Asian patients with newly diagnosed mantle-cell lymphoma
title_short Bortezomib-based therapy for transplant-ineligible East Asian patients with newly diagnosed mantle-cell lymphoma
title_sort bortezomib-based therapy for transplant-ineligible east asian patients with newly diagnosed mantle-cell lymphoma
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6039072/
https://www.ncbi.nlm.nih.gov/pubmed/30013367
http://dx.doi.org/10.2147/OTT.S150339
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