INT71164
From wiki-pain
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Sentences Mentioned In
Key: | Protein | Mutation | Event | Anatomy | Negation | Speculation | Pain term | Disease term |
As TPT progressed, the magnitude and lability of CV responses as well as frequency of VVS were reduced. | |||||||||||||||
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For instance,
we detected Dps, a DNA-binding protein that protects DNA during stress; Daigle et al. also identified dps using selective capture of transcribed sequence (SCOTS) technology to analyze S. | |||||||||||||||
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Instructions for the patient need to include information about the symptoms of PDSS, the avoidance of driving or operating machinery.20 | |||||||||||||||
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However, 2 patients treated with olanzapine LAI experienced PDSS following possible inadvertent intravascular injection. | |||||||||||||||
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The combination PLD/weekly PTX was well tolerated, as was the PLD/vinorelbine combination. 104 In contrast, PLD/TPT, even if tested at different doses of the two drugs, was characterized by an unacceptable rate of severe anemia (48%), leukopenia (70%), and thrombocytopenia (44%).102
PLD: phase III studies | |||||||||||||||
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More mature survival analysis confirmed the long-term advantage for platinum-sensitive patients receiving PLD vs TPT (median OS = 27 months vs 17.5 months, hazard ratio [HR] = 1.432, P value = 0.017).108 Moreover, for partially platinum-sensitive disease (n = 122), the HR favored PLD vs TPT (HR = 1.58, P value = 0.021). | |||||||||||||||
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At this time, available data support the phase II-derived suggestions that in platinum-resistant disease none of the currently most frequently used drugs, such as PLD, GEM, or TPT, shows superiority over the others in terms of response rate and survival; in this context the 3-week schedule of administration of PLD at 40 mg/m2 seems to offer the most favorable toxicity profile, which is likely to sustain the achievement of better QoL scores, at least in comparison to GEM.110 | |||||||||||||||
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Associations of increased intakes and/or in vivo levels of industrially-produced trans FAs with CHD risk are well established [29], whereas little information exists for eicosadienoic acid. | |||||||||||||||
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Modulation of p53 expression by red wine and its polyphenolic contents was studied on three human breast cancer cell lines and one colon cancer line by Soleas et al. (2001), which showed that these polyphenols, including quercetin, catechin, trans-resveratrol and caffeic acid did not affect p53 gene expression in two of the breast cancer lines. | |||||||||||||||
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