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dc.contributor.authorCurran, Desmond
dc.contributor.authorPozzo, Carmelo
dc.contributor.authorZaluski, Jerzy
dc.contributor.authorDank, Magdalena
dc.contributor.authorBarone, Carlo
dc.contributor.authorValvere, Vahur
dc.contributor.authorYalcin, Suayib
dc.contributor.authorPeschel, Christian
dc.contributor.authorWenczl, Miklós
dc.contributor.authorGoker, Erdem
dc.contributor.authorBugat, Roland
dc.date.accessioned2010-03-12T15:41:25Z
dc.date.available2010-03-12T15:41:25Z
dc.date.issued2009-09
dc.identifier.citationQuality of life of palliative chemotherapy naive patients with advanced adenocarcinoma of the stomach or esophagogastric junction treated with irinotecan combined with 5-fluorouracil and folinic acid: results of a randomised phase III trial. 2009, 18 (7):853-61 Qual Life Resen
dc.identifier.issn1573-2649
dc.identifier.pmid19568958
dc.identifier.doi10.1007/s11136-009-9493-z
dc.identifier.urihttp://hdl.handle.net/10147/94216
dc.description.abstractPURPOSE: The quality of life (QL) of advanced gastric cancer patients receiving irinotecan, folinic acid and 5-fluorouracil (5-FU) (IF arm) or cisplatin with 5-FU (CF arm) is presented. METHODS: Patients with measurable or evaluable advanced gastric cancer received IF weekly for 6/7 weeks or CF q4 weeks. QL was assessed using the EORTC QLQ-C30 at baseline, subsequently every 8 weeks until progression and thereafter every 3 months until death. The QL data were analysed using several statistical methods including summary measures and pattern-mixture modelling. RESULTS: A total of 333 patients were randomised and treated (IF 170, CF 163). The time-to-progression for IF and CF was 5.0 and 4.2 months (P = 0.088), respectively. The overall compliance rates for QL questionnaire completion were 60 and 56% in the IF and CF arms, respectively. Significant treatment differences were observed for the physical functioning scale (P = 0.024), nausea\vomiting (P = 0.001) and EQ-5D thermometer (P = 0.020) in favour of the IF treatment arm. CONCLUSION: There was a trend in favour of IF over CF in time-to-progression. The IF group also demonstrated a better safety profile than CF and a better QL on a number of multi-item scales, suggesting that IF offers an alternative first-line platinum-free treatment option for advanced gastric cancer.
dc.language.isoenen
dc.subject.meshAdenocarcinoma
dc.subject.meshAdolescent
dc.subject.meshAdult
dc.subject.meshAged
dc.subject.meshAntineoplastic Combined Chemotherapy Protocols
dc.subject.meshCamptothecin
dc.subject.meshCisplatin
dc.subject.meshEsophagogastric Junction
dc.subject.meshFluorouracil
dc.subject.meshHumans
dc.subject.meshLeucovorin
dc.subject.meshMiddle Aged
dc.subject.meshNeoplasm Metastasis
dc.subject.meshPalliative Care
dc.subject.meshQuality of Life
dc.subject.meshStomach Neoplasms
dc.subject.meshYoung Adult
dc.titleQuality of life of palliative chemotherapy naive patients with advanced adenocarcinoma of the stomach or esophagogastric junction treated with irinotecan combined with 5-fluorouracil and folinic acid: results of a randomised phase III trial.en
dc.contributor.departmentOmega Research, Santry, Dublin 9, Ireland. currandes@omega-research.eu.comen
dc.identifier.journalQuality of life research : an international journal of quality of life aspects of treatment, care and rehabilitationen
refterms.dateFOA2018-08-31T04:59:41Z
html.description.abstractPURPOSE: The quality of life (QL) of advanced gastric cancer patients receiving irinotecan, folinic acid and 5-fluorouracil (5-FU) (IF arm) or cisplatin with 5-FU (CF arm) is presented. METHODS: Patients with measurable or evaluable advanced gastric cancer received IF weekly for 6/7 weeks or CF q4 weeks. QL was assessed using the EORTC QLQ-C30 at baseline, subsequently every 8 weeks until progression and thereafter every 3 months until death. The QL data were analysed using several statistical methods including summary measures and pattern-mixture modelling. RESULTS: A total of 333 patients were randomised and treated (IF 170, CF 163). The time-to-progression for IF and CF was 5.0 and 4.2 months (P = 0.088), respectively. The overall compliance rates for QL questionnaire completion were 60 and 56% in the IF and CF arms, respectively. Significant treatment differences were observed for the physical functioning scale (P = 0.024), nausea\vomiting (P = 0.001) and EQ-5D thermometer (P = 0.020) in favour of the IF treatment arm. CONCLUSION: There was a trend in favour of IF over CF in time-to-progression. The IF group also demonstrated a better safety profile than CF and a better QL on a number of multi-item scales, suggesting that IF offers an alternative first-line platinum-free treatment option for advanced gastric cancer.


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