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“showed a trend”

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In the literature

While MEKiAUTO ( NCT04214418 ) showed the combination of mitogen-activated protein kinase kinase inhibitor (MEKi) cobimetinib, HCQ, and PD-L1 inhibitor Atezolizumab demonstrated limited tolerability and efficacy in patients with advanced KRAS-mutated pancreatic ductal adenocarcinoma, clinical benefit was observed in 36% of patients, while all of whom achieved stable disease as their best response; and patients with KRAS G12R mutations showed a trend toward improved overall survival (OS) compared to those with KRAS non-G12R mutations ( 77 ).
The multiple comparison of the time spent in close interaction during the social novelty phase showed a significant preference for the new unfamiliar mouse compared to the familiar one in HTZ adult females, whereas WT females showed a trend toward preference for the new unfamiliar mouse (100.1 ± 10.0 s HTZ with unfamiliar; 60.1 ± 6.6 s HTZ with familiar; 62.3 ± 5.2 s WT with unfamiliar; 41.5 ± 3.5 s WT with familiar; two‐way ANOVA, F (1.44) = 20.19, p < 0.0001 for cylinder effect, F (1.44) = 17.47, p = 0.0001 for genotype effect and F (1.44) = 2.016, p = 0.1627 for genotype × cylinder interaction; Sidak's post hoc test: WT familiar vs. unfamiliar p = 0.19, HTZ familiar vs. unfamiliar p = 0.0008, WT unfamiliar vs.
Our results showed a trend of improved inhibitory control only at the post-training periods in both ICNIC group (SSRT; visual: 111.54 ± 23.09 ms, auditory: 102.23 ± 50.96 ms) and non-training control group (SSRT; visual: 101.62 ± 29.72 ms, auditory: 93.74 ± 36.90 ms) when compared within groups.
Accordingly, control PASMCs exposed to recombinant WFDC2 showed a trend toward increased expression levels of FOXM1 , BIRC5 (also called Survivin), and IL1 β ( Supplemental Figure S3 ), all of which are critically involved in pulmonary vascular remodeling in PAH. 27 , 28 , 29 In addition, although not statistically significant, exposure of control PASMCs to the prohypertensive factors TNF-α or PDGF-BB increased expression of WFDC2 ( Supplemental Figure S3 ).
72 Intriguingly, the subgroup of patients who had increased bone turnover at 6 mo (CTx > mean reference-range) showed a trend for greater BMD gains on treatment, and despite a second dose of zoledronic acid, lost 5% BMD at spine and alarmingly 10% of this group experienced VFs. 29 Conversely, achieving CTx below this threshold 6 mo after an initial zoledronic acid dose was a reliable indicator for subsequent BMD preservation.