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dc.contributor.authorMauri, D.en
dc.contributor.authorPolyzos, N. P.en
dc.contributor.authorSalanti, G.en
dc.contributor.authorPavlidis, Nicholasen
dc.contributor.authorIoannidis, J. P. A.en
dc.creatorMauri, D.en
dc.creatorPolyzos, N. P.en
dc.creatorSalanti, G.en
dc.creatorPavlidis, Nicholasen
dc.creatorIoannidis, J. P. A.en
dc.date.accessioned2018-06-22T09:54:02Z
dc.date.available2018-06-22T09:54:02Z
dc.date.issued2008
dc.identifier.urihttps://gnosis.library.ucy.ac.cy/handle/7/42158
dc.description.abstractBackground: Many systemic nonhormonal regimens have been evaluated across several hundreds of randomized trials in advanced breast cancer. We aimed to quantify the relative merits of these regimens in prolonging survival. Methods: We performed a systematic review of all trials that compared different regimens involving chemotherapy and/or targeted therapy in advanced breast cancer (1973-2007). Regimens were categorized a priori into different treatment types. We performed multiple-treatments meta-analysis and calculated hazard ratios for each treatment category relative to monotherapy with old agents (ie, regimens not including anthracyclines, anthracenediones, vinorelbine, gemcitabine, capecitabine, taxanes, marimastat, thalidomide, trastuzumab, lapatinib, or bevacizumab). Results: We identified 370 eligible randomized trials (54 189 patients), of which 172 (31 552 patients) compared different types of treatment. Survival data from 148 comparisons pertaining to 128 of the 172 trials (26 031 patients, 22 different types of treatment) were available for inclusion in the multiple-treatments meta-analysis. Compared with single-agent chemotherapy with old nonanthracycline drugs, anthracycline regimens achieved 22%-33% relative risk reductions in mortality (ie, hazard ratio [HR] for standard-dose anthracycline-based combination: 0.67, 95% credibility interval [CrI] 0.57-0.78). Several newer regimens achieved further benefits (eg, HR [95% CrI] 0.67 [0.55-0.81] for single-drug taxane, 0.64 [0.53-0.78] for combination of anthracyclines with taxane, 0.49 [0.37-0.67] for taxane-based combination with capecitabine or gemcitabine), and similar benefits were seen with several regimens including molecular targeted treatments. Most regimens had very similar efficacy profiles (<5% difference in HR) as first- and subsequent-line therapies. Conclusions: Stepwise improvements in efficacy of chemotherapy and targeted treatments cumulatively have achieved major improvements in the survival of patients with advanced breast cancer. Many options that can be used in first and subsequent lines of therapy have comparable efficacy profiles. © The Author 2008. Published by Oxford University Press.en
dc.language.isoengen
dc.sourceJournal of the National Cancer Instituteen
dc.subjectArticleen
dc.subjectAdulten
dc.subjectFemaleen
dc.subjectAntineoplastic agentsen
dc.subjectHumanen
dc.subjectAgeden
dc.subjectHumansen
dc.subjectBreast canceren
dc.subjectBreast neoplasmsen
dc.subjectMiddle ageden
dc.subjectCancer combination chemotherapyen
dc.subjectPriority journalen
dc.subjectAntineoplastic combined chemotherapy protocolsen
dc.subjectClinical trialen
dc.subjectControlled clinical trialen
dc.subjectDrug efficacyen
dc.subjectGemcitabineen
dc.subjectMonotherapyen
dc.subjectTaxane derivativeen
dc.subjectTaxoidsen
dc.subjectTreatment outcomeen
dc.subjectSurvival analysisen
dc.subjectRandomized controlled trialen
dc.subjectCancer mortalityen
dc.subjectMitoxantroneen
dc.subjectSystematic reviewen
dc.subjectLapatiniben
dc.subjectTrastuzumaben
dc.subjectMeta analysisen
dc.subjectOdds ratioen
dc.subjectStatisticalen
dc.subjectSurvival timeen
dc.subjectRandomized controlled trials as topicen
dc.subjectResearch designen
dc.subjectAnthracycline derivativeen
dc.subjectBevacizumaben
dc.subjectAntimetabolitesen
dc.subjectAntineoplasticen
dc.subjectDeoxycytidineen
dc.subjectLow drug doseen
dc.subjectCapecitabineen
dc.subjectAntibioticsen
dc.subjectAnthracyclineen
dc.subjectAnthracyclinesen
dc.subjectFluorouracilen
dc.subjectData interpretationen
dc.titleMultiple-treatments meta-analysis of chemotherapy and targeted therapies in advanced breast canceren
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1093/jnci/djn414
dc.description.volume100
dc.description.issue24
dc.description.startingpage1780
dc.description.endingpage1791
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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