Show simple item record

dc.contributor.authorKaplan, S.en
dc.contributor.authorHanauske, A. R.en
dc.contributor.authorPavlidis, Nicholasen
dc.contributor.authorBruntsch, U.en
dc.contributor.authorVelde, A. Teen
dc.contributor.authorWanders, J.en
dc.contributor.authorHeinrich, B.en
dc.contributor.authorVerweij, J.en
dc.creatorKaplan, S.en
dc.creatorHanauske, A. R.en
dc.creatorPavlidis, Nicholasen
dc.creatorBruntsch, U.en
dc.creatorVelde, A. Teen
dc.creatorWanders, J.en
dc.creatorHeinrich, B.en
dc.creatorVerweij, J.en
dc.date.accessioned2018-06-22T09:53:44Z
dc.date.available2018-06-22T09:53:44Z
dc.date.issued1996
dc.identifier.urihttps://gnosis.library.ucy.ac.cy/handle/7/41994
dc.description.abstractIn a multicentre trial of the EORTC-Early Clinical Trials Group (ECTG) we treated 31 chemotherapy-naive patients with advanced non-small-cell lung cancer (NSCLC) with rhizoxin, a novel tubulin-binding agent. The drug was given as an i.v. bolus injection at 2 mg m-2 once every 3 weeks in an outpatient setting. Prophylactic antiemetics were not routinely given. Of the 29 eligible patients, nine had been treated surgically and three had received radiotherapy. The main toxic effects observed were stomatitis (34% of cycles) and neutropenia (41% of cycles). Neutropenic fever was rare (3% of cycles). Twenty-seven patients were evaluable for response. There were four partial responses (15%), while 13 patients (48%) showed stabilisation of their disease. The median duration of response was 7 months (range 6.0-10.7 months) and median survival from the start of rhizoxin treatment was 6 months (range 2-14.7 months). Rhizoxin as single agent shows activity in patients with advanced NSCLC.en
dc.language.isoengen
dc.sourceBritish journal of canceren
dc.subjectArticleen
dc.subjectAntineoplastic agenten
dc.subjectCancer chemotherapyen
dc.subjectHumanen
dc.subjectHumansen
dc.subjectAdulten
dc.subjectAgeden
dc.subjectFemaleen
dc.subjectMiddle ageden
dc.subjectCancer survivalen
dc.subjectPriority journalen
dc.subjectAlopeciaen
dc.subjectAnemiaen
dc.subjectClinical articleen
dc.subjectClinical trialen
dc.subjectDiarrheaen
dc.subjectLeukopeniaen
dc.subjectMulticenter studyen
dc.subjectNeutropeniaen
dc.subjectPhase 2 clinical trialen
dc.subjectStomatitisen
dc.subjectThrombocytopeniaen
dc.subjectAntineoplastic activityen
dc.subjectDrug hypersensitivityen
dc.subjectFeveren
dc.subjectLung neoplasmsen
dc.subjectLung non small cell canceren
dc.subjectCarcinomaen
dc.subjectMalaiseen
dc.subjectMaleen
dc.subjectIntravenous drug administrationen
dc.subjectVomitingen
dc.subjectBlood toxicityen
dc.subjectNauseaen
dc.subjectAntineoplasticen
dc.subjectPhase iien
dc.subjectSkin toxicityen
dc.subjectHeadacheen
dc.subjectNon-small-cell lungen
dc.subjectOutpatienten
dc.subjectAntibioticsen
dc.subjectNon-small-cell lung canceren
dc.subjectHematopoiesisen
dc.subjectLactonesen
dc.subjectMacrolidesen
dc.subjectRhizoxinen
dc.subjectPhlebitisen
dc.titleSingle agent activity of rhizoxin in non-small-cell lung cancer: A phase II trial of the EORTC early clinical trials groupen
dc.typeinfo:eu-repo/semantics/article
dc.description.volume73
dc.description.issue3
dc.description.startingpage403
dc.description.endingpage405
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


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record