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dc.contributor.authorPapageorgiou, E.en
dc.contributor.authorTsirigotis, P.en
dc.contributor.authorDimopoulos, M. A.en
dc.contributor.authorPavlidis, Nicholasen
dc.contributor.authorFountzilas, Georgeen
dc.contributor.authorPapageorgiou, S.en
dc.contributor.authorEconomopoulos, T.en
dc.creatorPapageorgiou, E.en
dc.creatorTsirigotis, P.en
dc.creatorDimopoulos, M. A.en
dc.creatorPavlidis, Nicholasen
dc.creatorFountzilas, Georgeen
dc.creatorPapageorgiou, S.en
dc.creatorEconomopoulos, T.en
dc.date.accessioned2018-06-22T09:54:12Z
dc.date.available2018-06-22T09:54:12Z
dc.date.issued2005
dc.identifier.urihttps://gnosis.library.ucy.ac.cy/handle/7/42235
dc.description.abstractTo investigate the efficacy and toxicity of the combination of gemcitabine and vinorelbine in patients with relapsed or refractory diffuse large B-cell lymphoma (DLBL), 22 patients with relapsed or refractory DLBL were treated with gemcitabine 1000 mg/m2 and vinorelbine 30 mg/m2 on days 1 and 8 every 3 wk for a maximum of six cycles. Fourteen patients were considered chemosensitive while eight patients were considered chemoresistant to the last treatment regimen. All 22 patients were assessed for response to treatment. Three patients (14%) achieved complete remission and eight patients (36%) had partial remission of their disease, with an overall response rate of 50%. With a median follow up of 44 months, the median time to progression (TTP) for all patients was 8.1 months while the median overall survival (OS) was 12.9 months. Toxicity was minimal and all patients were treated on an outpatient basis. The combination of gemcitabine and vinorelbine is an effective and well-tolerated regimen for patients with relapsed of refractory DLBL. © Blackwell Munksgaard 2005.en
dc.language.isoengen
dc.sourceEuropean journal of haematologyen
dc.subjectArticleen
dc.subjectCisplatinen
dc.subjectCyclophosphamideen
dc.subjectCytarabineen
dc.subjectEtoposideen
dc.subjectHumanen
dc.subjectPrednisoneen
dc.subjectVincristineen
dc.subject80 and overen
dc.subjectAgeden
dc.subjectHumansen
dc.subjectAdulten
dc.subjectAgeden
dc.subjectControlled studyen
dc.subjectFemaleen
dc.subjectMiddle ageden
dc.subjectCancer combination chemotherapyen
dc.subjectCancer growthen
dc.subjectCancer survivalen
dc.subjectFollow upen
dc.subjectPriority journalen
dc.subjectAlopeciaen
dc.subjectAnemiaen
dc.subjectAntineoplastic combined chemotherapy protocolsen
dc.subjectBone marrow suppressionen
dc.subjectClinical articleen
dc.subjectClinical trialen
dc.subjectControlled clinical trialen
dc.subjectDrug efficacyen
dc.subjectFebrile neutropeniaen
dc.subjectLeukopeniaen
dc.subjectMethylprednisoloneen
dc.subjectMucosa inflammationen
dc.subjectMulticenter studyen
dc.subjectNavelbineen
dc.subjectNeurotoxicityen
dc.subjectNeutropeniaen
dc.subjectPhase 2 clinical trialen
dc.subjectStomatitisen
dc.subjectThrombocytopeniaen
dc.subjectVinblastineen
dc.subjectVinorelbineen
dc.subjectSalvage therapyen
dc.subjectSurvival analysisen
dc.subjectFeveren
dc.subjectGranulocyte colony stimulating factoren
dc.subjectTreatment outcomeen
dc.subjectCancer relapseen
dc.subjectRelapseen
dc.subjectB cell lymphomaen
dc.subjectEpirubicinen
dc.subjectMaleen
dc.subjectB-cellen
dc.subjectDiffuseen
dc.subjectLarge cell lymphomaen
dc.subjectLarge-cellen
dc.subjectLymphomaen
dc.subjectSide effecten
dc.subjectVomitingen
dc.subjectNauseaen
dc.subjectIfosfamideen
dc.subjectDeoxycytidineen
dc.subjectGemcitabineen
dc.subjectCancer regressionen
dc.subjectRemission inductionen
dc.subjectChemosensitivityen
dc.subjectMitoguazoneen
dc.subjectRefractoryen
dc.titleCombination chemotherapy with gemcitabine and vinorelbine in the treatment of relapsed or refractory diffuse large B-cell lymphoma: A phase-II trial by the Hellenic Cooperative Oncology Groupen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1111/j.1600-0609.2005.00482.x
dc.description.volume75
dc.description.issue2
dc.description.startingpage124
dc.description.endingpage129
dc.author.facultyΙατρική Σχολή / Medical School
dc.author.departmentΙατρική Σχολή / Medical School
dc.type.uhtypeArticleen
dc.contributor.orcidPavlidis, Nicholas [0000-0002-2195-9961]
dc.gnosis.orcid0000-0002-2195-9961


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