Department of Medicine, Stanford University School of Medicine, Stanford, California, USA.
Department of Medicine, VA Palo Alto Health Care System/Stanford University, Palo Alto, California, USA.
JCI Insight. 2018 Oct 18;3(20):123775. doi: 10.1172/jci.insight.123775.
Lymphedema is a common condition affecting millions around the world that still lacks approved medical therapy. Because ketoprofen, an NSAID, has been therapeutic in experimental lymphedema, we evaluated its efficacy in humans.
We first performed an exploratory open-label trial. Patients with either primary or secondary lymphedema received ketoprofen 75 mg by mouth 3 times daily for 4 months. Subjects were evaluated for changes in histopathology, with skin thickness, limb volume, and tissue bioimpedance changes serving as secondary endpoints. Based on our encouraging findings, we next conducted a placebo-controlled trial, with the primary outcome defined as a change in skin thickness, as measured by skin calipers. Secondary endpoints for this second study included histopathology, limb volume, bioimpedance, and systemic inflammatory mediators.
We enrolled 21 lymphedema patients in the open-label trial, from November 2010 to July 2011. Histopathology and skin thickness were significantly improved at 4 months compared with baseline. In the follow-up, double-blind, placebo-controlled trial, we enrolled 34 patients from August 2011 to October 2015, with 16 ketoprofen recipients and 18 placebo-treated subjects. No serious adverse events occurred. The ketoprofen recipients demonstrated reduced skin thickness, as well as improved composite measures of histopathology and decreased plasma granulocyte CSF (G-CSF) expression.
These 2 exploratory studies together support the utility of targeted antiinflammatory therapy with ketoprofen in patients with lymphedema. Our results highlight the promise of such approaches to help restore a failing lymphatic circulation.
ClinicalTrials.gov NCT02257970.
淋巴水肿是一种常见病症,影响着全球数百万人,但其仍缺乏被批准的医学疗法。由于非甾体抗炎药(NSAID)酮洛芬在实验性淋巴水肿中具有治疗作用,我们评估了其在人类中的疗效。
我们首先进行了一项探索性、开放性标签试验。原发性或继发性淋巴水肿患者每天口服酮洛芬 75mg,每日 3 次,持续 4 个月。通过皮肤厚度、肢体体积和组织生物阻抗变化等作为次要终点,评估患者的组织病理学变化。基于我们的研究结果,我们进行了一项安慰剂对照试验,主要结局定义为皮肤卡尺测量的皮肤厚度变化。该第二项研究的次要终点包括组织病理学、肢体体积、生物阻抗和全身炎症介质。
我们于 2010 年 11 月至 2011 年 7 月间共招募了 21 名淋巴水肿患者参与开放性标签试验。与基线相比,4 个月时组织病理学和皮肤厚度均显著改善。在后续的、双盲、安慰剂对照试验中,我们于 2011 年 8 月至 2015 年 10 月共招募了 34 名患者,其中 16 名接受酮洛芬治疗,18 名接受安慰剂治疗。未发生严重不良事件。酮洛芬治疗组的皮肤厚度减少,组织病理学综合指标改善,血浆粒细胞集落刺激因子(G-CSF)表达降低。
这两项探索性研究共同支持了在淋巴水肿患者中使用酮洛芬进行靶向抗炎治疗的有效性。我们的研究结果强调了这种方法在帮助恢复衰竭的淋巴循环方面的应用前景。
ClinicalTrials.gov NCT02257970。