Legendre Paul, Blanchet Benoit, Porcher Raphael, Bérezné Alice, Allard Marie, London Jonathan, Terrier Benjamin, Cohen Pascal, Le Jeunne Claire, Mouthon Luc
Service de Médecine Interne, Hôpital Cochin, Centre de Référence pour les Maladies Systémiques Autoimmunes Rares d'Ile de France, DHU Authors, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
UF de Pharmacocinétique et Pharmacochimie, Hôpital Cochin, AP-HP, Paris, France.
J Scleroderma Relat Disord. 2021 Feb;6(1):87-95. doi: 10.1177/2397198320944342. Epub 2020 Aug 6.
To explore pharmacokinetic/pharmacodynamic relationship between mycophenolic acid area under the curve and clinical response at 1 year on skin involvement or interstitial lung disease in patients with systemic sclerosis.
Retrospective, monocentric study based on French Scleroderma Database in patients receiving mycophenolate mofetil who experienced a limited sampling strategy to estimate individual mycophenolic acid area under the curve plus two pulmonary function tests and skin evaluation after 1 month and 1 year. Efficacy criterions were variations of modified Rodnan skin score, forced vital capacity, and diffusing lung capacity for carbon monoxide at 1 year.
We included 52 patients; mean age was 49 years (range 17-79), and 36 (69%) were females. Fifty patients (96%) had skin sclerosis, 39 (75%) had diffuse skin involvement with a median modified Rodnan skin score of 14 (0-38). Thirty-eight (76%) had interstitial lung disease, with median forced vital capacity and diffusing lung capacity for carbon monoxide of 81% (37-127) and 56% (28-103) from predicted values, respectively. Twenty-five (51%) patients had pulmonary fibrosis. Mycophenolate mofetil was given for 10 months (0-173) at a median dose of 2000 mg/day (500-3000). In the entire population, no relationship was found between area under the curve and modified Rodnan skin score (p = 0.085), forced vital capacity (p = 0.80), or diffusing lung capacity for carbon monoxide (p = 0.72) variations at 1 year.
In this retrospective study, we failed to document any relationship between mycophenolic acid area under the curve and skin involvement or interstitial lung disease evolution. Routine monitoring of mycophenolic acid in systemic sclerosis patients treated with mycophenolate mofetil cannot be recommended based on our results.
探讨霉酚酸曲线下面积与系统性硬化症患者皮肤受累或间质性肺病1年临床反应之间的药代动力学/药效学关系。
基于法国硬皮病数据库进行的回顾性单中心研究,研究对象为接受霉酚酸酯治疗的患者,采用有限采样策略估计个体霉酚酸曲线下面积,同时在1个月和1年后进行两项肺功能测试及皮肤评估。疗效标准为1年后改良Rodnan皮肤评分、用力肺活量和一氧化碳弥散量的变化。
我们纳入了52例患者;平均年龄为49岁(范围17 - 79岁),36例(69%)为女性。50例(96%)有皮肤硬化,39例(75%)有弥漫性皮肤受累,改良Rodnan皮肤评分中位数为14(0 - 38)。38例(76%)有间质性肺病,用力肺活量和一氧化碳弥散量中位数分别为预测值的81%(37 - 127)和56%(28 - 103)。25例(51%)患者有肺纤维化。霉酚酸酯给药10个月(0 - 173),中位剂量为2000 mg/天(500 - 3000)。在整个人群中,未发现曲线下面积与1年后改良Rodnan皮肤评分变化(p = 0.085)、用力肺活量(p = 0.80)或一氧化碳弥散量变化(p = 0.72)之间存在相关性。
在这项回顾性研究中,我们未能证明霉酚酸曲线下面积与皮肤受累或间质性肺病进展之间存在任何关系。基于我们的研究结果,不建议对接受霉酚酸酯治疗的系统性硬化症患者进行霉酚酸的常规监测。