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口服布地奈德泡腾片治疗口腔慢性移植物抗宿主病的疗效观察:一项开放、随机、多中心研究。

Improvement in oral chronic graft-versus-host disease with the administration of effervescent tablets of topical budesonide-an open, randomized, multicenter study.

机构信息

Department of Oral Medicine, Hebrew University-Hadassah School of Dental Medicine, Jerusalem, Israel.

出版信息

Biol Blood Marrow Transplant. 2012 Jan;18(1):134-40. doi: 10.1016/j.bbmt.2011.06.001. Epub 2011 Jun 12.

Abstract

Chronic graft-versus-host disease (cGVHD) frequently involves oral tissues. Although the mucosal changes may be painful and impair oral function, there is currently no topical therapy available for oral cGVHD that has been proven to work in an evidence-based manner. The aims of this study were to (1) assess the response of patients with oral cGVHD to various doses of a new topical budesonide formulation; (2) evaluate the efficacy and safety of the new topical budesonide formulation in these patients. An open, randomized, multicenter phase II pilot study with 4 treatment arms differing in application frequency and duration was performed. Response to treatment was scored by the clinician and patient using several scales. Oral cGVHD improved in all patients, with a median reduction of 70%. Pain reduction was similar in all study arms. The rate of objective improvement (defined as ≥50%) was not significantly different among the 4 study arms. The safety profile was satisfactory. Topical budesonide mouthwash (3 mg/10 mL) improved oral cGVHD in all patients when applied for 5 or 10 minutes, 2 or 3 times daily. The response was similar in all treatment arms. Safety analysis supported a dosing schedule of 3 mg of budesonide 3 times a day for 10 minutes.

摘要

慢性移植物抗宿主病(cGVHD)常累及口腔组织。尽管黏膜变化可能引起疼痛并影响口腔功能,但目前尚无经证实有效的口腔 cGVHD 局部治疗方法。本研究旨在:(1)评估不同剂量新型布地奈德口腔制剂治疗口腔 cGVHD 的效果;(2)评估该新型口腔布地奈德制剂在这些患者中的疗效和安全性。这是一项开放、随机、多中心的 2 期临床试验,设有 4 个治疗组,应用频率和持续时间不同。采用多种量表由临床医生和患者对治疗反应进行评分。所有患者的口腔 cGVHD 均有改善,中位数缓解率为 70%。所有研究组的疼痛缓解情况相似。4 个研究组的客观改善率(定义为≥50%)无显著差异。安全性良好。新型布地奈德口腔漱液(3mg/10mL)每天应用 2 或 3 次,每次 5 或 10 分钟,可改善所有患者的口腔 cGVHD。所有治疗组的反应相似。安全性分析支持每日 3 次、每次 3mg 布地奈德,持续 10 分钟的给药方案。

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