Université de Rennes, CHU Rennes, Inserm, EHESP, Irset (Institut de recherche en santé, environnement et travail)-UMR_S 1085, 35000 Rennes, France; Inserm, centre d'investigation clinique, CIC 1414, 35000 Rennes, France.
Clinical pharmacology department, Nantes university hospital, 44000 Nantes, France; UMR Inserm 1235, The Enteric Nervous System in Gut and Brain Disorders, University of Nantes, 44000 Nantes, France.
Therapie. 2022 Sep-Oct;77(5):509-521. doi: 10.1016/j.therap.2022.03.005. Epub 2022 Apr 20.
Nirmatrelvir in association with ritonavir (PAXLOVID™, Pfizer) is an antiviral agent targeting the 3-chymotrypsin-like cysteine protease enzyme (3C-like protease or Mpro) which is a key enzyme of the viral cycle of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). This combination with a well-known pharmacokinetic enhancer leads to a high risk for drug-drug interactions in a polymedicated elected population for treatment. The aim of this work was to provide recommendations on behalf of the national French society of pharmacology (French Society of Pharmacology and Therapeutics; SFPT), by suggesting optimal and pragmatic therapeutic strategies if nirmatrelvir/ritonavir is to be given together with drugs commonly used, in order to ensure secured physicians' prescription.
Six clinical pharmacologists search the scientific literature to provide a first draft of recommendations. Thereafter, twelve other clinical pharmacologists verified the recommendations and proposed modifications. The final draft was then validated by all 18 participants.
Five distinct recommendations were issued: i) contra-indications, ii) "PAXLOVID™ not recommended with the comedication", iii) "PAXLOVID™ possible whether the comedication is discontinued", iv) "PAXLOVID™ possible only after an expert advice" and v) "PAXLOVID™ possible without modification of the associated treatment". The final document comprises recommendations for 171 drugs/therapeutic classes aiming to secure prescription. In complex situations, clinicians are advised to contact their pharmacology department to obtain specific recommendations on the management of drug-drug interactions with nirmatrelvir/ritonavir.
These recommendations intend to be a help for clinicians willing to prescribe nirmatrelvir/ritonavir and to prevent drug-drug interactions leading to adverse drug reactions or loss of efficacy. They constitute a guideline for primary care situations. Of course, some complex situations may require expert advices and here, again, clinical pharmacologists are at the forefront in providing therapeutic advice.
尼马曲韦与利托那韦(PAXLOVID™,辉瑞)联合使用是一种针对 3-糜蛋白酶样半胱氨酸蛋白酶(3CL 样蛋白酶或 Mpro)的抗病毒药物,3CL 样蛋白酶是严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)病毒周期的关键酶。这种与众所周知的药代动力学增强剂的联合使用,在选择用于治疗的多药物治疗人群中会导致药物相互作用的风险很高。这项工作的目的是代表法国国家药理学学会(法国药理学与治疗学学会;SFPT)提出建议,如果要将尼马曲韦/利托那韦与常用药物联合使用,建议选择最佳和实用的治疗策略,以确保医生安全处方。
六名临床药理学家搜索科学文献,提供建议初稿。此后,另外十二名临床药理学家对建议进行了核实并提出了修改意见。最终草案由所有 18 名参与者进行了验证。
提出了五条不同的建议:i)禁忌,ii)“不建议将 PAXLOVID™与联合用药一起使用”,iii)“如果停止联合用药,则可以使用 PAXLOVID™”,iv)“只有在专家建议后才能使用 PAXLOVID™”和 v)“可以在不改变联合治疗的情况下使用 PAXLOVID™”。最终文件包含了 171 种药物/治疗类别的建议,旨在确保处方安全。在复杂情况下,临床医生应联系其药理学部门,以获得有关尼马曲韦/利托那韦与药物相互作用管理的具体建议。
这些建议旨在为愿意开具尼马曲韦/利托那韦的临床医生提供帮助,并防止因药物相互作用导致不良反应或疗效丧失。它们构成了初级保健情况的指南。当然,一些复杂的情况可能需要专家建议,在这里,临床药理学家再次处于提供治疗建议的最前沿。