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甲氨蝶呤治疗肉样瘤病:六年大样本队列研究中遇到的血液学和肝脏毒性。

Methotrexate in sarcoidosis: hematologic and hepatic toxicity encountered in a large cohort over a six year period.

机构信息

University of Cincinnati Medical Center, Cincinnati, OH, USA.

ild care foundation research team, Ede, the Netherlands.

出版信息

Sarcoidosis Vasc Diffuse Lung Dis. 2020;37(3):e2020001. doi: 10.36141/svdld.v37i3.9362. Epub 2020 Sep 30.

DOI:10.36141/svdld.v37i3.9362
PMID:33264378
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7690061/
Abstract

BACKGROUND

Methotrexate (MTX) is a second line agent for treatment of sarcoidosis. Its long term safety and efficacy in sarcoidosis remains unclear.

METHODS

This was a retrospective review of patients seen at the University of Cincinnati Sarcoidosis Clinic over a six year period. For each visit, complete blood count, liver function testing, and dosing and outcome of MTX was noted. For efficacy, we compared the outcome of therapy of a matching subgroup of patients treated with either MTX or infliximab for one year and results scored as improved, stable, or worse based on response of the target organ.

RESULTS

Over six years, 1606 sarcoidosis patients were seen with a total of 13,576 clinical visits. During the study period, 607 patients (38% of total) were receiving MTX and had available blood work. Moderate elevation of alanine aminotransferase (ALT) (>3 times upper limit normal) was seen in nine (1.6%) patients. White blood count of <1500 cells per cu mm was seen in one patient. At six months, over half of the 44 patients initiated on infliximab and with at least six months of follow-up were better, while only 23% of the 44 of a matched subset of MTX treated patients were better (Chi square=10.566, p=0.0143). At the 12 month assessment, the infliximab treated patients were still more likely to be better than those treated with MTX (Chi square=10.033, p=0.0183). Only 23% of those treated with MTX were worse at twelve months.

CONCLUSION

In our study, MTX therapy was associated with very few hepatic or hematologic complications. MTX was less likely than infliximab to improve clinical status. However, only 20% were worse after one year of MTX. .

摘要

背景

甲氨蝶呤(MTX)是治疗类肉瘤病的二线药物。其在类肉瘤病中的长期安全性和疗效尚不清楚。

方法

这是一项在辛辛那提大学类肉瘤病诊所就诊的患者的回顾性研究,时间跨度为六年。对于每次就诊,都记录了全血细胞计数、肝功能检查以及 MTX 的剂量和结果。为了评估疗效,我们比较了接受 MTX 或英夫利昔单抗治疗一年的匹配亚组患者的治疗结果,并根据靶器官的反应将结果评为改善、稳定或恶化。

结果

在六年期间,共观察到 1606 例类肉瘤病患者,共进行了 13576 次临床就诊。在研究期间,有 607 例(占总数的 38%)患者正在接受 MTX 治疗,并且有可用的血液检查结果。9 例(1.6%)患者出现丙氨酸氨基转移酶(ALT)中度升高(>正常上限的 3 倍)。1 例患者的白细胞计数<1500 个/立方毫米。在 6 个月时,超过一半的 44 例开始接受英夫利昔单抗治疗且有至少 6 个月随访的患者情况更好,而在接受 MTX 治疗的 44 例匹配亚组患者中,只有 23%的患者情况更好(卡方=10.566,p=0.0143)。在 12 个月评估时,接受英夫利昔单抗治疗的患者仍然比接受 MTX 治疗的患者更有可能情况更好(卡方=10.033,p=0.0183)。只有 23%的接受 MTX 治疗的患者在 12 个月时情况更差。

结论

在我们的研究中,MTX 治疗与很少的肝或血液学并发症相关。MTX 改善临床状况的可能性低于英夫利昔单抗。然而,只有 20%的患者在接受 MTX 治疗一年后情况更差。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3662/7690061/49a2daa226af/SVDLD-37-1-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3662/7690061/41246581490c/SVDLD-37-1-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3662/7690061/49a2daa226af/SVDLD-37-1-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3662/7690061/41246581490c/SVDLD-37-1-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3662/7690061/49a2daa226af/SVDLD-37-1-g002.jpg

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