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dc.contributor.authorSamantas, E.en
dc.contributor.authorSkarlos, Dimosthenis V.en
dc.contributor.authorPectasides, Dimitriosen
dc.contributor.authorNikolaidis, Pavlosen
dc.contributor.authorKalofonos, H. P.en
dc.contributor.authorMylonakis, N.en
dc.contributor.authorVardoulakis, Then
dc.contributor.authorKosmidis, Paraskevas A.en
dc.contributor.authorPavlidis, Nicholasen
dc.contributor.authorFountzilas, Georgeen
dc.creatorSamantas, E.en
dc.creatorSkarlos, Dimosthenis V.en
dc.creatorPectasides, Dimitriosen
dc.creatorNikolaidis, Pavlosen
dc.creatorKalofonos, H. P.en
dc.creatorMylonakis, N.en
dc.creatorVardoulakis, Then
dc.creatorKosmidis, Paraskevas A.en
dc.creatorPavlidis, Nicholasen
dc.creatorFountzilas, Georgeen
dc.date.accessioned2018-06-22T09:53:07Z
dc.date.available2018-06-22T09:53:07Z
dc.date.issued1999
dc.identifier.urihttps://gnosis.library.ucy.ac.cy/handle/7/41665
dc.description.abstractSixty patients with poor prognostic features, either with extensive disease (ED) or limited disease (LD) small cell lung cancer (SCLC), were treated on an out-patient basis with Carboplatin 80 mg/m2 weekly for 3 weeks and oral Etoposide, at a dose of 100 mg, every other day for 21 days. The treatment was repeated every 5 weeks. Responding patients with LD were also treated with thoracic irradiation and those who achieved complete response (CR) received prophylactic cranial radio-therapy. The overall response rate (RR) was 32.1% with 8.9% CR. The responses were better for LD (RR 58.3%, CR 25%, partial response, PR 33.3%), than those for ED (RR 25%, CR 4.5%, PR 20.5%). The median time to progression (TTP) was 4.8 months and the median survival 5.5 months. These poor results could be attributed to the bad performance status and the presence of visceral and brain metastases in this group of patients. The results could also be due to the lower maximum concentration (C(max)) and higher T(1/2) of Etoposide, as measured in the blood and urine probably due to the modified regimen used in our study and to the organ insufficiency in this selected group of patients. Although, toxicity was generally mild and manageable, two toxic deaths occurred. In conclusion, this regimen appears to have a lower efficacy in terms of response and survival than that obtained in other studies using Cisplatin or Carboplatin plus Etoposide in a similar way. Therapy with this regimen, though less toxic, may not be a reliable alternative in elderly patients with visceral metastases and ECOG performance status ≥2. Copyright (C) 1999 Elsevier Science Ireland Ltd.en
dc.language.isoengen
dc.sourceLung Canceren
dc.subjectAdministrationen
dc.subjectArticleen
dc.subjectCisplatinen
dc.subjectHumanen
dc.subject80 and overen
dc.subjectAgeden
dc.subjectHumansen
dc.subjectAdulten
dc.subjectAgeden
dc.subjectFemaleen
dc.subjectMajor clinical studyen
dc.subjectMiddle ageden
dc.subjectCancer survivalen
dc.subjectChemotherapyen
dc.subjectDisease progressionen
dc.subjectPriority journalen
dc.subjectPrognosisen
dc.subjectAlopeciaen
dc.subjectAnemiaen
dc.subjectAntiemetic agenten
dc.subjectAntineoplastic combined chemotherapy protocolsen
dc.subjectClinical trialen
dc.subjectLeukopeniaen
dc.subjectNeutropeniaen
dc.subjectOndansetronen
dc.subjectThrombocytopeniaen
dc.subjectEtoposideen
dc.subjectOralen
dc.subjectSurvival analysisen
dc.subjectArea under the curveen
dc.subjectDrug administration scheduleen
dc.subjectLung neoplasmsen
dc.subjectLung small cell canceren
dc.subjectAntibiotic agenten
dc.subjectCancer radiotherapyen
dc.subjectCarcinomaen
dc.subjectMaleen
dc.subjectCarboplatinen
dc.subjectIntravenous drug administrationen
dc.subjectVomitingen
dc.subjectNauseaen
dc.subjectRisk assessmenten
dc.subjectDrug clearanceen
dc.subjectDrug blood levelen
dc.subjectCombined modality therapyen
dc.subjectSmall cellen
dc.subjectOral drug administrationen
dc.subjectDrug bioavailabilityen
dc.subjectDrug distributionen
dc.subjectElectrocorticographyen
dc.subjectSmall cell lung carcinomaen
dc.titleCombination chemotherapy with low doses of weekly Carboplatin and oral Etoposide in poor risk small cell lung canceren
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1016/S0169-5002(98)00095-6
dc.description.volume23
dc.description.issue2
dc.description.startingpage159
dc.description.endingpage168
dc.author.facultyΙατρική Σχολή / Medical School
dc.author.departmentΙατρική Σχολή / Medical School
dc.type.uhtypeArticleen
dc.contributor.orcidPavlidis, Nicholas [0000-0002-2195-9961]
dc.contributor.orcidKalofonos, H. P. [0000-0002-3286-778X]
dc.gnosis.orcid0000-0002-2195-9961
dc.gnosis.orcid0000-0002-3286-778X


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