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视黄醛,一种维生素A类似物,在膀胱癌化学预防试验中的眼部效应。

Ocular effects of fenretinide, a vitamin A analog, in a chemoprevention trial of bladder cancer.

作者信息

Baglietto L, Torrisi R, Arena G, Tosetti F, Gonzaga A G, Pasquetti W, Robertson C, Decensi A

机构信息

Division of Epidemiology and Biostatistics, European Institute of Oncology, Milan, Italy.

出版信息

Cancer Detect Prev. 2000;24(4):369-75.

Abstract

Fenretinide is a vitamin A derivative under investigation in cancer prevention trials. Because all available pharmacologic and toxicologic data were obtained from breast cancer patients, we measured plasma drug, metabolite, and vitamin A levels and studied their relationship with visual and ocular symptoms in a cohort formed mostly by male subjects belonging to a bladder cancer prevention trial. After 1 year, the mean plasma retinol levels (+/- standard deviation [SD]) were 168.2 +/- 75.8 ng/ml in 31 subjects treated with fenretinide and 594.5 +/- 168.4 ng/ml in 36 control subjects (P < .001). Plasma retinol levels were correlated inversely to drug and metabolite concentrations, which in turn were correlated inversely to the interval from last drug intake. The decline of plasma vitamin A levels accounted for a 41.7% cumulative incidence of diminished dark adaptability in the retinoid arm as compared to 6.8% in the control arm (odds ratio = 13.8; 95% confidence interval, 2.9-66.1). Although compliance as assessed by capsule count was high, three subjects originally assigned to the treatment group who proved to be noncompliers (8.8%, or 3 of 34) had no detectable plasma drug or metabolite levels. Our data confirm the specific pharmacologic and visual effects of fenretinide also in a male population and strengthen the importance of multiple blood measurements to monitor treatment compliance in prevention trials.

摘要

芬维A胺是一种正在癌症预防试验中进行研究的维生素A衍生物。由于所有可用的药理学和毒理学数据均来自乳腺癌患者,我们在一个主要由膀胱癌预防试验中的男性受试者组成的队列中,测量了血浆药物、代谢物和维生素A水平,并研究了它们与视觉和眼部症状的关系。1年后,31名接受芬维A胺治疗的受试者的平均血浆视黄醇水平(±标准差[SD])为168.2±75.8 ng/ml,36名对照受试者的平均血浆视黄醇水平为594.5±168.4 ng/ml(P<.001)。血浆视黄醇水平与药物和代谢物浓度呈负相关,而药物和代谢物浓度又与上次服药后的时间间隔呈负相关。与对照组6.8%的累积发生率相比,类视黄醇组血浆维生素A水平的下降导致暗适应能力下降的累积发生率为41.7%(优势比=13.8;95%置信区间,2.9-66.1)。尽管通过胶囊计数评估的依从性很高,但最初分配到治疗组的三名被证明不依从的受试者(34名中的3名,占8.8%)血浆中未检测到药物或代谢物水平。我们的数据证实了芬维A胺在男性人群中也具有特定的药理学和视觉效应,并强化了在预防试验中多次进行血液检测以监测治疗依从性的重要性。

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