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dc.contributor.authorSymonds, R P
dc.contributor.authorDavidson, Susan E
dc.contributor.authorChan, S
dc.contributor.authorReed, N S
dc.contributor.authorMcMahon, T
dc.contributor.authorRai, D
dc.contributor.authorHarden, S
dc.contributor.authorPaul, J
dc.date.accessioned2012-06-15T17:39:16Z
dc.date.available2012-06-15T17:39:16Z
dc.date.issued2011-10
dc.identifier.citationSCOTCERV: a phase II trial of docetaxel and gemcitabine as second line chemotherapy in cervical cancer. 2011, 123 (1):105-9 Gynecol. Oncol.en_GB
dc.identifier.issn1095-6859
dc.identifier.pmid21723596
dc.identifier.doi10.1016/j.ygyno.2011.06.001
dc.identifier.urihttp://hdl.handle.net/10541/229168
dc.description.abstractThe aim of the study was to determine the response rate and response duration of cervical cancer previously treated by cisplatin (with or without radiation) to a combination of docetaxel and gemcitabine. Secondary endpoints were assessment of toxicity and quality of life (QoL) of patients receiving the treatment.
dc.language.isoenen
dc.rightsArchived with thanks to Gynecologic oncologyen_GB
dc.subject.meshAdult
dc.subject.meshAntineoplastic Combined Chemotherapy Protocols
dc.subject.meshCisplatin
dc.subject.meshDeoxycytidine
dc.subject.meshDrug Resistance, Neoplasm
dc.subject.meshFemale
dc.subject.meshHumans
dc.subject.meshMiddle Aged
dc.subject.meshNeoadjuvant Therapy
dc.subject.meshNeoplasm Recurrence, Local
dc.subject.meshQuality of Life
dc.subject.meshTaxoids
dc.subject.meshUterine Cervical Neoplasms
dc.titleSCOTCERV: a phase II trial of docetaxel and gemcitabine as second line chemotherapy in cervical cancer.en
dc.typeArticleen
dc.contributor.departmentUniversity of Leicester, Department of Cancer Studies & Molecular Medicine, Leicester, UK.en_GB
dc.identifier.journalGynecologic Oncologyen_GB
html.description.abstractThe aim of the study was to determine the response rate and response duration of cervical cancer previously treated by cisplatin (with or without radiation) to a combination of docetaxel and gemcitabine. Secondary endpoints were assessment of toxicity and quality of life (QoL) of patients receiving the treatment.


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