Treatment allocation was not masked. Starting doses were 80% of standard doses, with discretionary escalation to full dose after 6 weeks. The two primary outcome measures were: addition of oxaliplatin ([A vs B] + [C vs D]), assessed with progression-free survival (PFS); and substitution of fluorouracil with capecitabine ([A vs C] + [B vs D]), assessed by change from baseline to 12 weeks in global quality of life (QoL). Analysis was by intention to treat. Baseline clinical and CHA data were modelled against outcomes with a novel composite measure, overall treatment utility (OTU). This study is registered,
number ISRCTN21221452.\n\nFindings 459 patients were randomly assigned (115 to each of groups A C, 114 to group D). Factorial comparison of addition of oxaliplatin versus no addition Selleck Quisinostat LY3023414 suggested some improvement in PFS, but the finding was not significant (median 5.8 months [IQR 3.3-7.5] vs 4.5 months [2.8-6.4]; hazard ratio 0.84, 95% CI 0-69-1.01, p=0.07). Replacement of fluorouracil with capecitabine did not improve global QoL: 69 of 124 (56%) patients receiving fluorouracil reported improvement in global QoL compared with 69 of 123 (56%) receiving capecitabine. The risk of having any grade 3 or worse toxic effect was not significantly increased with oxaliplatin (83/219 [38%] vs 70/221 [32%]; p=0.17), but
was higher with capecitabine than with fluorouracil (88/222 [40 4] vs 65/218 [30%]; p=0.03). In multivariable analysis, fewer baseline symptoms (odds ratio 1.32, 95% CI 1.14-1.52), less Selleck Quizartinib widespread disease (1.51, 1.05-2-19), and use of oxaliplatin (0.57, 0.39-0.82) were predictive of better OTU.\n\nInterpretation FOCUS2 shows that with an appropriate design, including reduced starting doses of chemotherapy, frail and elderly patients can participate in a randomised controlled trial. On balance, a combination including oxaliplatin was preferable to single-agent fluoropyrimidines, although
the primary endpoint of PFS was not met. Capecitabine did not improve QoL compared with fluorouracil. Comprehensive baseline assessment holds promise as an objective predictor of treatment benefit.”
“Objectives: Oncogene addiction has provided therapeutic opportunities in many human malignancies, but molecular targeted therapy for oral squamous cell carcinoma (OSCC) is not yet available. In this study, we attempted to identify an appropriate target molecule for treatment of patients with OSCC.\n\nMaterials and methods: Microarray analysis was performed to determine the gene expression profiles in nine human OSCC cell lines and a non-neoplastic keratinocyte cell line. The expression levels of Aurora kinase A (AURKA) mRNA and protein in human OSCC cells and tissues were examined.