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Article: NK/T-cell lymphomas

TitleNK/T-cell lymphomas
Authors
KeywordsNK/T-cell lymphoma
Nasal
Non-nasal
EBV
PET/CT
Issue Date2019
PublisherBailliere Tindall. The Journal's web site is located at http://www.elsevier.com/locate/issn/15216926
Citation
Best Practice & Research: Clinical Haematology, 2019, v. 32 n. 3, p. 253-261 How to Cite?
AbstractNK/T-cell lymphomas are extranodal EBV-related malignancies, mostly of NK-cell and occasionally of T-cell lineage. They are divided into nasal, non-nasal, and disseminated subtypes. Nasal NK/T-cell lymphomas involve the nose, nasopharynx and the upper aerodigestive tract. Non-nasal NK/T-cell lymphomas involve the skin, gastrointestinal tract, testis and other sites. Disseminated NK/T-cell lymphoma involves multiple organs, and may present with a leukemic phase. Initial evaluation requires positron emission tomography computed tomography (PET/CT) and quantification of circulating EBV DNA. Radiotherapy alone is inadequate with frequent relapses. Anthracycline-containing regimens are ineffective. Regimens incorporating asparaginase are currently the standard. For stage I/II disease, combined chemotherapy and radiotherapy is recommended. For stage III/IV disease, asparaginase-containing regimens are needed. Autologous hematopoietic stem cell transplantation (HSCT) is of limited efficacy, whereas allogeneic HSCT may be useful in patients with stage III/IV and relapsed diseases. Immunotherapy with antibodies against CD30, programmed cell death protein 1 and CD38 is promising.
Persistent Identifierhttp://hdl.handle.net/10722/289386
ISSN
2023 Impact Factor: 2.2
2023 SCImago Journal Rankings: 0.864
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorTse, E-
dc.contributor.authorKwong, YL-
dc.date.accessioned2020-10-22T08:11:55Z-
dc.date.available2020-10-22T08:11:55Z-
dc.date.issued2019-
dc.identifier.citationBest Practice & Research: Clinical Haematology, 2019, v. 32 n. 3, p. 253-261-
dc.identifier.issn1521-6926-
dc.identifier.urihttp://hdl.handle.net/10722/289386-
dc.description.abstractNK/T-cell lymphomas are extranodal EBV-related malignancies, mostly of NK-cell and occasionally of T-cell lineage. They are divided into nasal, non-nasal, and disseminated subtypes. Nasal NK/T-cell lymphomas involve the nose, nasopharynx and the upper aerodigestive tract. Non-nasal NK/T-cell lymphomas involve the skin, gastrointestinal tract, testis and other sites. Disseminated NK/T-cell lymphoma involves multiple organs, and may present with a leukemic phase. Initial evaluation requires positron emission tomography computed tomography (PET/CT) and quantification of circulating EBV DNA. Radiotherapy alone is inadequate with frequent relapses. Anthracycline-containing regimens are ineffective. Regimens incorporating asparaginase are currently the standard. For stage I/II disease, combined chemotherapy and radiotherapy is recommended. For stage III/IV disease, asparaginase-containing regimens are needed. Autologous hematopoietic stem cell transplantation (HSCT) is of limited efficacy, whereas allogeneic HSCT may be useful in patients with stage III/IV and relapsed diseases. Immunotherapy with antibodies against CD30, programmed cell death protein 1 and CD38 is promising.-
dc.languageeng-
dc.publisherBailliere Tindall. The Journal's web site is located at http://www.elsevier.com/locate/issn/15216926-
dc.relation.ispartofBest Practice & Research: Clinical Haematology-
dc.subjectNK/T-cell lymphoma-
dc.subjectNasal-
dc.subjectNon-nasal-
dc.subjectEBV-
dc.subjectPET/CT-
dc.titleNK/T-cell lymphomas-
dc.typeArticle-
dc.identifier.emailTse, E: ewctse@hku.hk-
dc.identifier.emailKwong, YL: ylkwong@hkucc.hku.hk-
dc.identifier.authorityTse, E=rp00471-
dc.identifier.authorityKwong, YL=rp00358-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/j.beha.2019.06.005-
dc.identifier.pmid31585625-
dc.identifier.scopuseid_2-s2.0-85067188447-
dc.identifier.hkuros317069-
dc.identifier.volume32-
dc.identifier.issue3-
dc.identifier.spage253-
dc.identifier.epage261-
dc.identifier.isiWOS:000494882700007-
dc.publisher.placeUnited Kingdom-
dc.identifier.issnl1521-6926-

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