Katial R K, Stelzle R C, Bonner M W, Marino M, Cantilena L R, Smith L J
Department of Allergy and Immunology, Walter Reed Army Medical Center, Washington, DC 20307, USA.
Arch Intern Med. 1998;158(15):1713-5. doi: 10.1001/archinte.158.15.1713.
The apparent low adverse effect profile of the new drug zafirlukast has made it an attractive choice in the treatment of asthma. We present the first case (to our knowledge) of a potentially serious drug-drug interaction between zafirlukast and theophylline. A 15-year-old white girl with asthma had been taking theophylline (Slo-bid, Rhone-Poulenc Rorer Pharmaceuticals Inc, Collegeville, Pa) (300 mg twice daily), with drug levels of approximately 61 micromol/L (11.0 microg/mL) for several years. Recently, her serum theophylline levels had increased to the toxic range (133.2 micromol/L [24 microg/mL]) shortly after the addition of zafirlukast (Accolate, Zeneca Pharmaceuticals, Wilmington, Del) to her regimen. Attempts were made to stop and then restart the theophylline therapy at progressively lower doses; however, with each attempt, the patient's reaction to the drug became more toxic, with serum theophylline levels ranging between 99.9 and 149.9 micromol/L (18 and 27 microg/mL). So this potential drug-drug interaction could be investigated, the patient stopped taking both drugs for 1 week. Then, she again started taking theophylline (75 mg twice daily), and over 2 days reached a steady state serum theophylline level of 12.8 to 14.4 micromol/L (2.3-2.6 microg/mL). On the third day, zafirlukast (20 mg twice daily) was reintroduced to the regimen, and the theophylline therapy was continued. By the fifth day, a dramatic 7-fold increase was seen in the serum theophylline level (101.6 micromol/L [18.3 microg/mL]). The areas under the curve for theophylline alone and theophylline with zafirlukast were 29.3 and 197 (mg x h)/L, respectively. One explanation for the noted increase in the theophylline level is that metabolism occurs mainly by cytochrome P450 (CYP 1A2), an enzyme that is known to be inhibited with high concentrations of zafirlukast. Although the current metabolism of the 2 drugs in combination is poorly understood, the potential for serious interactions seems to exist in the rapidly growing population of persons with asthma, for whom they may be prescribed. The noted increase in the theophylline level after zafirlukast administration is in contrast to the original reports by the manufacturer. Therefore, we recommend that physicians evaluate serum theophylline levels closely when prescribing the 2 drugs in combination.
新药扎鲁司特明显的低不良反应特征使其成为治疗哮喘的一个有吸引力的选择。据我们所知,我们首次报告了扎鲁司特与茶碱之间可能存在的严重药物相互作用病例。一名15岁患哮喘的白人女孩多年来一直服用茶碱(Slo-bid,罗纳普朗克罗瑞尔制药公司,宾夕法尼亚州科尔奇维尔)(每日两次,每次300毫克),药物水平约为61微摩尔/升(11.0微克/毫升)。最近,在她的治疗方案中加用扎鲁司特(Accolate,捷利康制药公司,特拉华州威尔明顿)后不久,她的血清茶碱水平升至中毒范围(133.2微摩尔/升[24微克/毫升])。尝试停用然后以逐渐降低的剂量重新开始茶碱治疗;然而,每次尝试时,患者对该药物的反应毒性都更大,血清茶碱水平在99.9至149.9微摩尔/升(18至27微克/毫升)之间。为了研究这种潜在的药物相互作用,患者停用两种药物1周。然后,她再次开始服用茶碱(每日两次,每次75毫克),并在2天内达到了12.8至14.4微摩尔/升(2.3 - 2.6微克/毫升)的稳态血清茶碱水平。第三天,将扎鲁司特(每日两次,每次20毫克)重新引入治疗方案,并继续进行茶碱治疗。到第五天,血清茶碱水平出现了惊人的7倍增长(101.6微摩尔/升[18.3微克/毫升])。单独使用茶碱和与扎鲁司特联合使用时茶碱的曲线下面积分别为29.3和197(毫克·小时)/升。茶碱水平显著升高的一种解释是,其代谢主要通过细胞色素P450(CYP 1A2)进行,已知高浓度的扎鲁司特会抑制这种酶。尽管目前对这两种药物联合使用时的代谢情况了解甚少,但在可能同时开具这两种药物的哮喘患者快速增长的人群中,似乎存在严重相互作用的可能性。扎鲁司特给药后茶碱水平的显著升高与制造商最初的报告相反。因此,我们建议医生在联合开具这两种药物时密切评估血清茶碱水平。