Gavrysyuk Volodymyr, Merenkova Ievgenia, Dziublyk Yaroslav, Morska Nataliia, Pendalchuk Nataliia, Bychenko Olesia, Vlasova Nataliia
Department of Interstitial Lung Diseases, National Institute of Phthisiology and Pulmonology Named after F. G. Yanovsky, 10, M. Amosova str., 03038 Kyiv, Ukraine.
Department of Differential Diagnosis of Tuberculosis and Nonspecific Lung Deseases, National Institute of Phthisiology and Pulmonology Named after F. G. Yanovsky, 10, M. Amosova str., 03038 Kyiv, Ukraine.
Diagnostics (Basel). 2021 Jul 19;11(7):1289. doi: 10.3390/diagnostics11071289.
There is insufficient information in the literature on the comparative efficacy and tolerability of methotrexate (MTX) and methylprednisolone (MP) in patients with pulmonary sarcoidosis in assessing primary outcomes and the relapse rate.
The aim of our study was to evaluate primary and long-term outcomes of using MTX and MP in patients with pulmonary sarcoidosis.
A total of 143 patients with newly diagnosed pulmonary sarcoidosis, verified by high-resolution computed tomography (CT) data, were examined. Corticosteroid (CS) therapy was used in 97 patients using MP at a dose of 0.4 mg/kg body weight for 4 weeks, followed by a dose reduction to 0.1 mg/kg by the end of the sixth month. The total duration of CS therapy was 12 months on average. Forty-six patients were treated with MTX at a dose of 10 mg/week (28) and 15 mg/week (18) per os for 6 to 12 months. The study of the relapse rate was conducted within 12 months after the CT data normalization in 60 patients after CS therapy and in 24 after MTX treatment.
MP treatment was successfully completed in 68 (70.1%), and MTX in 29 (60.4%) patients. In five MP patients (5.2%) and in five (10.9%) MTX, treatment was discontinued due to serious side effects. In seven (7.2%) MP patients and ten (21.7%) MTX patients, treatment required additional therapy due to the lack of efficacy. Progression with MP treatment (17-17.5%) was more common than with MTX (2-4.3%; Chi square = 4.703, = 0.031). Relapses after MP therapy were observed in 26 (43.3%) patients, and after MTX therapy in 2 (8.3%; Chi square = 9.450, = 0.003).
In patients with pulmonary sarcoidosis, MTX monotherapy does not differ significantly from MP monotherapy in terms of the level of efficacy and the rate of serious side effects. Increasing the MTX dose from 10 to 15 mg/week accelerates the rate of regression of sarcoidosis, improves treatment efficacy, and does not affect the rate of serious side effects. When using MTX, there is a significant decrease in the incidence of treatment resistance and the relapse rate.
关于甲氨蝶呤(MTX)和甲基强的松龙(MP)在评估肺结节病患者主要结局和复发率方面的比较疗效和耐受性,文献中的信息不足。
我们研究的目的是评估MTX和MP用于肺结节病患者的主要和长期结局。
共检查了143例经高分辨率计算机断层扫描(CT)数据证实的新诊断肺结节病患者。97例患者采用皮质类固醇(CS)治疗,使用MP,剂量为0.4mg/kg体重,持续4周,到第六个月末剂量减至0.1mg/kg。CS治疗的总持续时间平均为12个月。46例患者口服MTX治疗,剂量为每周10mg(28例)和每周15mg(18例),持续6至12个月。在60例接受CS治疗和24例接受MTX治疗的患者CT数据正常化后的12个月内进行复发率研究。
68例(70.1%)患者成功完成MP治疗,29例(60.4%)患者成功完成MTX治疗。5例MP患者(5.2%)和5例MTX患者(10.9%)因严重副作用而停药。7例(7.2%)MP患者和10例(21.7%)MTX患者因缺乏疗效而需要额外治疗。MP治疗的病情进展(17 - 17.5%)比MTX治疗更常见(2 - 4.3%;卡方 = 4.703,P = 0.031)。MP治疗后26例(43.3%)患者出现复发,MTX治疗后2例(8.3%)患者出现复发(卡方 = 9.450,P = 0.003)。
在肺结节病患者中,MTX单药治疗在疗效水平和严重副作用发生率方面与MP单药治疗无显著差异。将MTX剂量从每周10mg增加到15mg可加快结节病的消退速度,提高治疗效果,且不影响严重副作用的发生率。使用MTX时,治疗抵抗的发生率和复发率显著降低。