The diagnosis and management of NK/T-cell lymphomas
Abstract Extranodal natural killer (NK)/T-cell lymphoma is an aggressive malignancy of putative NK-cell origin, with a minority deriving from the T-cell lineage. Pathologically, the malignancy occurs in two forms, extranodal NK/T-cell lymphoma, nasal type; and aggressive NK-cell leukaemia. Lymphoma...
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doaj-43f4e40183be4b0aa619eece36d9e1582020-11-24T21:33:54ZengBMCJournal of Hematology & Oncology1756-87222017-04-0110111310.1186/s13045-017-0452-9The diagnosis and management of NK/T-cell lymphomasEric Tse0Yok-Lam Kwong1Department of Medicine, Professorial Block, Queen Mary HospitalDepartment of Medicine, Professorial Block, Queen Mary HospitalAbstract Extranodal natural killer (NK)/T-cell lymphoma is an aggressive malignancy of putative NK-cell origin, with a minority deriving from the T-cell lineage. Pathologically, the malignancy occurs in two forms, extranodal NK/T-cell lymphoma, nasal type; and aggressive NK-cell leukaemia. Lymphoma occur most commonly (80%) in the nose and upper aerodigestive tract, less commonly (20%) in non-nasal areas (skin, gastrointestinal tract, testis, salivary gland), and rarely as disseminated disease with a leukemic phase. Genetic analysis showed mutations of genes involved in the JAK/STAT pathway, RNA assembly, epigenetic regulation, and tumor suppression. In initial clinical evaluation, positron emission tomography computed tomography, and quantification of plasma EBV DNA are mandatory as they are useful for response monitoring and prognostication. In stage I/II diseases, combined chemotherapy and radiotherapy (sequentially or concurrently) is the best approach. Conventional anthracycline-containing regimens are ineffective and should be replaced by non-anthracycline-containing regimens, preferably including L-asparaginase. Radiotherapy alone is associated with high systemic relapse rates and should be avoided. In stage III/IV diseases, non-anthracycline-regimens-containing L-asparaginase are the standard. In relapsed/refractory cases, blockade of the programmed death protein 1 has recently shown promising results with high response rates. In the era of effective non-anthracycline-containing regimens, autologous haematopoietic stem cell transplantation (HSCT) has not been shown to be beneficial. However, allogeneic HSCT may be considered for high-risk or advanced-stage patients in remission or relapsed/refractory patients responding to salvage therapy. Prognostic models taking into account presentation, interim, and end-of-treatment parameters are useful in triaging patients to different treatment strategies.http://link.springer.com/article/10.1186/s13045-017-0452-9NK/T-cell lymphomaExtranodalNasalNon-nasalEBV DNA quantificationL-asparaginase |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Eric Tse Yok-Lam Kwong |
spellingShingle |
Eric Tse Yok-Lam Kwong The diagnosis and management of NK/T-cell lymphomas Journal of Hematology & Oncology NK/T-cell lymphoma Extranodal Nasal Non-nasal EBV DNA quantification L-asparaginase |
author_facet |
Eric Tse Yok-Lam Kwong |
author_sort |
Eric Tse |
title |
The diagnosis and management of NK/T-cell lymphomas |
title_short |
The diagnosis and management of NK/T-cell lymphomas |
title_full |
The diagnosis and management of NK/T-cell lymphomas |
title_fullStr |
The diagnosis and management of NK/T-cell lymphomas |
title_full_unstemmed |
The diagnosis and management of NK/T-cell lymphomas |
title_sort |
diagnosis and management of nk/t-cell lymphomas |
publisher |
BMC |
series |
Journal of Hematology & Oncology |
issn |
1756-8722 |
publishDate |
2017-04-01 |
description |
Abstract Extranodal natural killer (NK)/T-cell lymphoma is an aggressive malignancy of putative NK-cell origin, with a minority deriving from the T-cell lineage. Pathologically, the malignancy occurs in two forms, extranodal NK/T-cell lymphoma, nasal type; and aggressive NK-cell leukaemia. Lymphoma occur most commonly (80%) in the nose and upper aerodigestive tract, less commonly (20%) in non-nasal areas (skin, gastrointestinal tract, testis, salivary gland), and rarely as disseminated disease with a leukemic phase. Genetic analysis showed mutations of genes involved in the JAK/STAT pathway, RNA assembly, epigenetic regulation, and tumor suppression. In initial clinical evaluation, positron emission tomography computed tomography, and quantification of plasma EBV DNA are mandatory as they are useful for response monitoring and prognostication. In stage I/II diseases, combined chemotherapy and radiotherapy (sequentially or concurrently) is the best approach. Conventional anthracycline-containing regimens are ineffective and should be replaced by non-anthracycline-containing regimens, preferably including L-asparaginase. Radiotherapy alone is associated with high systemic relapse rates and should be avoided. In stage III/IV diseases, non-anthracycline-regimens-containing L-asparaginase are the standard. In relapsed/refractory cases, blockade of the programmed death protein 1 has recently shown promising results with high response rates. In the era of effective non-anthracycline-containing regimens, autologous haematopoietic stem cell transplantation (HSCT) has not been shown to be beneficial. However, allogeneic HSCT may be considered for high-risk or advanced-stage patients in remission or relapsed/refractory patients responding to salvage therapy. Prognostic models taking into account presentation, interim, and end-of-treatment parameters are useful in triaging patients to different treatment strategies. |
topic |
NK/T-cell lymphoma Extranodal Nasal Non-nasal EBV DNA quantification L-asparaginase |
url |
http://link.springer.com/article/10.1186/s13045-017-0452-9 |
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