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Article: The prognostic factors for peripheral T-cell lymphomas

TitleThe prognostic factors for peripheral T-cell lymphomas
Authors
KeywordsNon‐Hodgkin's lymphoma
T‐immunophenotype
Issue Date1992
PublisherJohn Wiley & Sons Ltd. The Journal's web site is located at http://www3.interscience.wiley.com/cgi-bin/jhome/3182
Citation
Hematological Oncology, 1992, v. 10 n. 3-4, p. 135-140 How to Cite?
AbstractThe peripheral T-cell lymphomas of 50 patients were classified by histological type and tumour cell size, the latter as described by the Nebraska Group. There was no difference in the pattern of their clinical features among the various histological subtypes and their clinical outcome was similar. Cell size and other factors including sex, age, presence of B symptoms, sites of primary disease, histological subtypes according to the Japanese classification, lactate dehydrogenase level and presence of bulky disease did not appear to correlate with clinical outcome. However, patients with stage IV disease had significantly lower CR rate (9/29 versus 16/21, p = 0.01) and poorer survival at 3 years (p = 0.05) than those with stage I, II and III disease. Patients receiving COPP, the less intensive chemotherapy regimen, appeared to have poorer clinical outcome but the difference observed was not statistically significant because of the number of patients in each subgroup.
Persistent Identifierhttp://hdl.handle.net/10722/161944
ISSN
2021 Impact Factor: 4.850
2020 SCImago Journal Rankings: 0.918
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLiang, Ren_US
dc.contributor.authorLoke, SLen_US
dc.contributor.authorChan, ACLen_US
dc.date.accessioned2012-09-05T05:16:12Z-
dc.date.available2012-09-05T05:16:12Z-
dc.date.issued1992en_US
dc.identifier.citationHematological Oncology, 1992, v. 10 n. 3-4, p. 135-140en_US
dc.identifier.issn0278-0232en_US
dc.identifier.urihttp://hdl.handle.net/10722/161944-
dc.description.abstractThe peripheral T-cell lymphomas of 50 patients were classified by histological type and tumour cell size, the latter as described by the Nebraska Group. There was no difference in the pattern of their clinical features among the various histological subtypes and their clinical outcome was similar. Cell size and other factors including sex, age, presence of B symptoms, sites of primary disease, histological subtypes according to the Japanese classification, lactate dehydrogenase level and presence of bulky disease did not appear to correlate with clinical outcome. However, patients with stage IV disease had significantly lower CR rate (9/29 versus 16/21, p = 0.01) and poorer survival at 3 years (p = 0.05) than those with stage I, II and III disease. Patients receiving COPP, the less intensive chemotherapy regimen, appeared to have poorer clinical outcome but the difference observed was not statistically significant because of the number of patients in each subgroup.en_US
dc.languageengen_US
dc.publisherJohn Wiley & Sons Ltd. The Journal's web site is located at http://www3.interscience.wiley.com/cgi-bin/jhome/3182en_US
dc.relation.ispartofHematological Oncologyen_US
dc.subjectNon‐Hodgkin's lymphoma-
dc.subjectT‐immunophenotype-
dc.subject.meshAge Factorsen_US
dc.subject.meshFemaleen_US
dc.subject.meshHong Kong - Epidemiologyen_US
dc.subject.meshHumansen_US
dc.subject.meshImmunophenotypingen_US
dc.subject.meshL-Lactate Dehydrogenase - Analysisen_US
dc.subject.meshLymphoma, T-Cell, Peripheral - Classification - Epidemiology - Pathologyen_US
dc.subject.meshMaleen_US
dc.subject.meshMiddle Ageden_US
dc.subject.meshNeoplasm Stagingen_US
dc.subject.meshPrognosisen_US
dc.subject.meshSex Factorsen_US
dc.subject.meshTumor Markers, Biological - Analysisen_US
dc.titleThe prognostic factors for peripheral T-cell lymphomasen_US
dc.typeArticleen_US
dc.identifier.emailLiang, R:rliang@hku.hken_US
dc.identifier.authorityLiang, R=rp00345en_US
dc.description.naturelink_to_subscribed_fulltexten_US
dc.identifier.doi10.1002/hon.2900100302en_US
dc.identifier.pmid1398509-
dc.identifier.scopuseid_2-s2.0-0026715203en_US
dc.identifier.volume10en_US
dc.identifier.issue3-4en_US
dc.identifier.spage135en_US
dc.identifier.epage140en_US
dc.identifier.isiWOS:A1992JU20700001-
dc.publisher.placeUnited Kingdomen_US
dc.identifier.scopusauthoridLiang, R=26643224900en_US
dc.identifier.scopusauthoridLoke, SL=7006559512en_US
dc.identifier.scopusauthoridChan, ACL=16047349300en_US
dc.identifier.issnl0278-0232-

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