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霉酚酸酯(骁悉®)联合低剂量泼尼松龙治疗中重度格雷夫斯眼眶病

Mycophenolate Mofetil (CellCept®) in Combination With Low Dose Prednisolone in Moderate to Severe Graves' Orbitopathy.

作者信息

Rajabi Mohammad Taher, Rafizadeh Seyed Mohsen, Mohammadi Abbas, Eshraghi Bahram, Mohammadi Nader, Hosseini Seyedeh Simindokht, Rajabi Mohammad Bagher, Keshmirshekan Mohammad Mohsen, Shahriari Mansoor, Poursayed Lazarjani Seyedeh Zahra, Parandin Mohammad Mehdi

机构信息

Eye Research Center, Farabi Eye Hospital, Tehran University of Medical Sciences, Tehran, Iran.

Department of Eye, Eye Research Center, Amiralmomenin Hospital, School of Medicin, Guilan University of Medical Science, Rasht, Iran.

出版信息

Front Med (Lausanne). 2022 Feb 11;9:788228. doi: 10.3389/fmed.2022.788228. eCollection 2022.

DOI:10.3389/fmed.2022.788228
PMID:35223896
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8873183/
Abstract

Although corticosteroids are currently the first-choice drug for thyroid eye disease (TED), in 20-30% of cases, patients show poor or non-existent responses, and when the drug is withdrawn, 10-20% of patients relapse. Thus, in this study, we aimed to investigate the efficacy of the combined use of mycophenolate mofetil (CellCept®) and low dose oral prednisolone in patients with moderate to severe Graves' orbitopathy (GO). For the first time, we investigated the relationship between TED-related parameters and proptosis reduction. In a prospective, non-randomized, interventional case series, 242 patients with moderate-to-severe GO were, assigned to receive oral prednisolone (5 mg/ d) and mycophenolate mofetil (CellCept®) (one 500 mg tablet twice per day according to the therapeutic response). The patients were monitored regularly during the 3rd, 6th, 12th, and 18th month of treatment. The main outcome measures were the clinical activity score (CAS), intraocular pressure (IOP), diplopia, proptosis and visual acuity. We also assessed the relationship between the main outcomes with proptosis changes and time to improvement (months). Adverse effects were recorded during each visit. The clinical response rate increased from 67.7% on the third month to 89.2% on the sixth month, and 94.2% on the 12th month. This therapeutic response continued until the 18th month of follow-up. The CAS responses [disease inactivation (CAS <3)] improved during our study: 70.6% on the third month, 90.0% on the sixth month, and 92.5% at 12th month. These conditions continued until the 18th month of follow-up. Proptosis improvement was 52% on the third month, 71% on the sixth month, 83% on the 12th month, and 87.1% on the 18th month. Changes in IOP and visual acuity were not significant ( = 0.568 and 0.668, respectively). The patient showed significant improvement in the Gorman score. A Shorter duration of treatment was seen in patients with earlier onset of intervention, younger age, and lack of all extraocular muscle (EOM) enlargement on computed tomography (CT) scan ( < 0.05). In addition, a better response (more reduction) in proptosis was related to: younger age at disease, earlier treatment intervention (less interval from the time the diagnosis of moderate-to-severe GO was made until medication initiation), shorter treatment time (less time to improvement), less IOP, lack of EOM enlargement on CT scan, and lack of diplopia ( < 0.05). Adverse events occurred in six patients. Findings show that mycophenolate mofetil (CellCept®) plus low-dose prednisolone can be introduced as a new optimal dosing regimen in GO due to its better effect on chronic complications such as proptosis and diplopia.

摘要

尽管目前皮质类固醇是甲状腺眼病(TED)的首选药物,但在20%至30%的病例中,患者表现出较差或无反应,并且在停药时,10%至20%的患者会复发。因此,在本研究中,我们旨在调查霉酚酸酯(骁悉®)与低剂量口服泼尼松龙联合使用对中度至重度格雷夫斯眼眶病(GO)患者的疗效。我们首次研究了TED相关参数与眼球突出度降低之间的关系。在一项前瞻性、非随机、干预性病例系列研究中,242例中度至重度GO患者被分配接受口服泼尼松龙(5毫克/天)和霉酚酸酯(骁悉®)(根据治疗反应,每天两次,每次一片500毫克)。在治疗的第3、6、12和18个月对患者进行定期监测。主要观察指标为临床活动评分(CAS)、眼压(IOP)、复视、眼球突出度和视力。我们还评估了主要观察指标与眼球突出度变化和改善时间(月)之间的关系。每次就诊时记录不良反应。临床缓解率从第3个月的67.7%增加到第6个月的89.2%,第12个月为94.2%。这种治疗反应一直持续到随访的第18个月。在我们的研究中,CAS反应[疾病失活(CAS<3)]有所改善:第3个月为70.6%,第6个月为90.0%,第12个月为92.5%。这些情况一直持续到随访的第18个月。第3个月眼球突出度改善率为52%,第6个月为71%,第12个月为83%,第18个月为87.1%。眼压和视力变化不显著(分别为=0.568和0.668)。患者的戈尔曼评分有显著改善。干预开始时间较早、年龄较小且计算机断层扫描(CT)显示所有眼外肌(EOM)均未增大的患者治疗时间较短(< = 0.568和0.668,分别)。患者的戈尔曼评分有显著改善。干预开始时间较早、年龄较小且计算机断层扫描(CT)显示所有眼外肌(EOM)均未增大的患者治疗时间较短(<0.05)。此外,眼球突出度更好的反应(更多降低)与以下因素有关:疾病发病时年龄较小、更早的治疗干预(从中度至重度GO诊断到开始用药的时间间隔更短)、更短的治疗时间(改善时间更短)、更低的眼压、CT扫描显示EOM未增大以及无复视(<0.05)。6例患者发生不良事件。研究结果表明,霉酚酸酯(骁悉®)加低剂量泼尼松龙可作为GO的一种新的最佳给药方案引入,因为它对眼球突出和复视等慢性并发症有更好的效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77fe/8873183/49a2c1df44d6/fmed-09-788228-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77fe/8873183/1524f3bcde41/fmed-09-788228-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77fe/8873183/3b33118cdf7c/fmed-09-788228-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77fe/8873183/49a2c1df44d6/fmed-09-788228-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77fe/8873183/1524f3bcde41/fmed-09-788228-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77fe/8873183/3b33118cdf7c/fmed-09-788228-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77fe/8873183/49a2c1df44d6/fmed-09-788228-g0003.jpg

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Real-World Efficacy and Safety of Mycophenolate Mofetil in Active Moderate-to-Sight-Threatening Thyroid Eye Disease.霉酚酸酯在活动性中度至重度威胁视力的甲状腺眼病中的真实世界疗效和安全性
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