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1 brentuximab vedotin and 65 to physician's choice), with 128 analysed in the intention-to-treat population (64 in each gro
5 eks post-treatment), assessed within each HCV genotype, and analysed in the intention-to-treat population.
6 utuzumab-ibrutinib versus standard chemoimmunotherapy, both analysed in the intention-to-treat population (ie, all patien
7 as the time from randomisation until death from any cause), analysed in the intention-to-treat population.
8 al response at 12 weeks (SVR12) after treatment completion, analysed in the intention-to-treat population.
9 unstable angina, and hospital admission for heart failure, analysed in the intention-to-treat population (all participan
12 n Test (WMFT) at the end of the 2 week intervention period, analysed in the intention-to-treat population.
13 were the safety and tolerability of the treatment regimen, analysed in the intention-to-treat population.
14 TEC-3 trial were overall survival and failure-free survival analysed in the intention-to-treat population.
15 The primary endpoint was progression-free survival analysed in the intention-to-treat population.
17 radiographic progression-free survival and overall survival analysed in the intention-to-treat population.
18 Criteria in Solid Tumours version 1.1 and overall survival analysed in the intention-to-treat population.
19 dpoints reported here are 5-year progression-free survival (analysed in the intention-to-treat population) and disease-fr
20 points were overall survival and progression-free survival, analysed in the intention-to-treat population (n=675), with d
21 The primary endpoint was overall survival, analysed in the intention-to-treat population, using a two-st
23 r glucose, and insulin from an oral glucose tolerance test) analysed in the intention-to-treat population.
24 ophil percentage from baseline to 12 weeks after treatment, analysed in the intention-to-treat population.
25 21 days after randomisation and, in our main analysis, was analysed in the intention-to-treat population, which comprise
26 nce-free survival, as assessed by the investigator, and was analysed in the intention-to-treat population.
27 rall survival was a prespecified secondary endpoint and was analysed in the intention-to-treat population.
32 of invasive and non-invasive IBTR as a first recurrence was analysed in the intention-to-treat population, excluding thos
36 orced expiratory volume in 1 s (FEV1) on day 169, which was analysed in the intention-to-treat population.
47 of BPI-SF item 3, and patient-reported outcomes (PROs) were analysed in the intention-to-treat population with baseline a
48 EORTC QLQ-C30, EORTC QLQ-MY20, and FACT-GP5 scores were analysed in the intention-to-treat population, and PRO-CTCAE
49 ant difference in disease-free survival between groups when analysed in the intention-to-treat population.
50 ified primary outcome was units of blood collected per year analysed in the intention-to-treat population.