A comprehensive retrospective cohort study of the journey of B-cell lymphoma in Taiwan
Abstract Complete disease journey and risk factors for poor outcomes are needed to facilitate effectiveness evaluations of new therapies and clinical decision-making in B-cell Non-Hodgkin lymphoma (B-NHL), particularly in Asia where such data are lacking. This retrospective cohort study used electro...
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Nature Portfolio
2021
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oai:doaj.org-article:b726675caf1f4b8b89a54c49ac26c15e2021-12-02T15:55:13ZA comprehensive retrospective cohort study of the journey of B-cell lymphoma in Taiwan10.1038/s41598-021-89316-y2045-2322https://doaj.org/article/b726675caf1f4b8b89a54c49ac26c15e2021-05-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-89316-yhttps://doaj.org/toc/2045-2322Abstract Complete disease journey and risk factors for poor outcomes are needed to facilitate effectiveness evaluations of new therapies and clinical decision-making in B-cell Non-Hodgkin lymphoma (B-NHL), particularly in Asia where such data are lacking. This retrospective cohort study used electronic medical records from a regional medical centre in southern Taiwan to follow-up 441 patients newly diagnosed with common B-NHL subtypes: Diffuse Large B-cell Lymphoma (DLBCL), Follicular Lymphoma (FL), Chronic Lymphocytic Leukaemia/Small Lymphocytic Lymphoma (CLL/SLL), Marginal Zone Lymphoma (MZL), Mantle Cell Lymphoma (MCL), and Waldenström macroglobulinemia (WM), between 01-Jan-2008 and 31-Dec-2013, until 31-Dec-2017. Treatment pathways were modelled using a Markov approach. Stage III/IV disease at diagnosis was frequent for patients with DLBCL, FL, MCL and WM. Hepatitis B surface antigen/hepatitis C virus seropositivity was 18.6%/12.3%. Clinical responses to 1st-line treatment were observed in 76.0% (DLBCL), 87.3% (FL), 86.0% (MZL), 60.0% (MCL), and 42.9% (WM) of patients. For DLBCL, disease control was achieved by ~ 50% after 1st-line, ~ 24% after 2nd-line, ~ 17% after 3rd-line. Patients with Stage III/IV DLBCL or age > 65 years at diagnosis had lower rates of active treatment, poorer disease control and higher mortality than patients with early stage disease or age ≤ 65 years. Disease flare < 6 months after 1st-line treatment was significantly associated with mortality. Despite good clinical response rates for some sub-types, survival remains poor. New treatments are needed to improve the outcome of B-NHL.Sung-Nan PeiMing-Chung WangMing-Chun MaChing-Yuan KuoChun-Kai LiaoHong QiuLee Anne RothwellYanfang LiuNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-12 (2021) |
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Medicine R Science Q Sung-Nan Pei Ming-Chung Wang Ming-Chun Ma Ching-Yuan Kuo Chun-Kai Liao Hong Qiu Lee Anne Rothwell Yanfang Liu A comprehensive retrospective cohort study of the journey of B-cell lymphoma in Taiwan |
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Abstract Complete disease journey and risk factors for poor outcomes are needed to facilitate effectiveness evaluations of new therapies and clinical decision-making in B-cell Non-Hodgkin lymphoma (B-NHL), particularly in Asia where such data are lacking. This retrospective cohort study used electronic medical records from a regional medical centre in southern Taiwan to follow-up 441 patients newly diagnosed with common B-NHL subtypes: Diffuse Large B-cell Lymphoma (DLBCL), Follicular Lymphoma (FL), Chronic Lymphocytic Leukaemia/Small Lymphocytic Lymphoma (CLL/SLL), Marginal Zone Lymphoma (MZL), Mantle Cell Lymphoma (MCL), and Waldenström macroglobulinemia (WM), between 01-Jan-2008 and 31-Dec-2013, until 31-Dec-2017. Treatment pathways were modelled using a Markov approach. Stage III/IV disease at diagnosis was frequent for patients with DLBCL, FL, MCL and WM. Hepatitis B surface antigen/hepatitis C virus seropositivity was 18.6%/12.3%. Clinical responses to 1st-line treatment were observed in 76.0% (DLBCL), 87.3% (FL), 86.0% (MZL), 60.0% (MCL), and 42.9% (WM) of patients. For DLBCL, disease control was achieved by ~ 50% after 1st-line, ~ 24% after 2nd-line, ~ 17% after 3rd-line. Patients with Stage III/IV DLBCL or age > 65 years at diagnosis had lower rates of active treatment, poorer disease control and higher mortality than patients with early stage disease or age ≤ 65 years. Disease flare < 6 months after 1st-line treatment was significantly associated with mortality. Despite good clinical response rates for some sub-types, survival remains poor. New treatments are needed to improve the outcome of B-NHL. |
format |
article |
author |
Sung-Nan Pei Ming-Chung Wang Ming-Chun Ma Ching-Yuan Kuo Chun-Kai Liao Hong Qiu Lee Anne Rothwell Yanfang Liu |
author_facet |
Sung-Nan Pei Ming-Chung Wang Ming-Chun Ma Ching-Yuan Kuo Chun-Kai Liao Hong Qiu Lee Anne Rothwell Yanfang Liu |
author_sort |
Sung-Nan Pei |
title |
A comprehensive retrospective cohort study of the journey of B-cell lymphoma in Taiwan |
title_short |
A comprehensive retrospective cohort study of the journey of B-cell lymphoma in Taiwan |
title_full |
A comprehensive retrospective cohort study of the journey of B-cell lymphoma in Taiwan |
title_fullStr |
A comprehensive retrospective cohort study of the journey of B-cell lymphoma in Taiwan |
title_full_unstemmed |
A comprehensive retrospective cohort study of the journey of B-cell lymphoma in Taiwan |
title_sort |
comprehensive retrospective cohort study of the journey of b-cell lymphoma in taiwan |
publisher |
Nature Portfolio |
publishDate |
2021 |
url |
https://doaj.org/article/b726675caf1f4b8b89a54c49ac26c15e |
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