Baran Timothy M, Bass David A, Christensen Laurie, Longbine Erica, Favella Maria D, Foster Thomas H, Sharma Ashwani K
medRxiv. 2023 Oct 16:2023.10.16.23297086. doi: 10.1101/2023.10.16.23297086.
Standard of care for abscess management includes image-guided percutaneous drainage and antibiotics. However, cure rates vary between patients and there is growing concern for antibiotic-resistant bacteria. Photodynamic therapy (PDT), which utilizes light-activated dyes to generate cytotoxic reactive species, could complement the standard of care by sterilizing the abscess at time of drainage.
The goal of this study was to perform a first in humans Phase 1 clinical study evaluating safety and feasibility of PDT with methylene blue (MB) at the time of percutaneous abscess drainage. This was accomplished through an open-label dose escalation study, with duration of light delivery escalated from 5-30 minutes.
We performed MB-PDT in 18 subjects undergoing percutaneous abscess drainage. Following standard of care drainage, 1 mg/mL MB was delivered for 10 minutes. MB was aspirated, and 1% lipid emulsion infused to homogenize light dose at the cavity wall. An optical fiber was advanced to the approximate center of the abscess for 665 nm laser illumination at 20 mW/cm .
MB-PDT at the time of abscess drainage was safe and feasible in all cases, with no evidence of fat embolism due to lipid emulsion or adverse reaction to MB observed. No study-related adverse or serious adverse events were encountered, and the procedure was well tolerated by all subjects. While the study was not designed or powered to determine efficacy, time to resolution of clinical symptoms was significantly decreased in subjects receiving higher fluences (p=0.028). Additionally, drainage catheter output post-procedure was decreased in subjects receiving higher fluences (ρ=-0.18), although this difference was not significant (p=0.43).
MB-PDT is a safe and feasible adjunct to image-guided percutaneous abscess drainage. Clinical measures indicate a dose-dependent response to PDT, motivating future Phase 2 studies evaluating the efficacy of MB-PDT in this patient population.
脓肿治疗的标准护理包括影像引导下经皮引流和使用抗生素。然而,患者之间的治愈率各不相同,并且对抗生素耐药菌的担忧日益增加。光动力疗法(PDT)利用光激活染料产生细胞毒性反应性物质,可在引流时对脓肿进行杀菌,从而补充标准护理。
本研究的目的是开展一项首例人体1期临床研究,评估在经皮脓肿引流时使用亚甲蓝(MB)进行光动力疗法的安全性和可行性。这是通过一项开放标签剂量递增研究完成的,光照射时间从5分钟递增至30分钟。
我们对18名接受经皮脓肿引流的受试者进行了MB-PDT。按照标准护理进行引流后,注入1mg/mL的MB,持续10分钟。吸出MB,注入1%的脂质乳剂以使腔壁的光剂量均匀化。将一根光纤推进到脓肿的大致中心,以20mW/cm²的功率进行665nm激光照射。
在所有病例中,脓肿引流时的MB-PDT都是安全可行的,未观察到因脂质乳剂导致的脂肪栓塞或对MB的不良反应。未遇到与研究相关的不良或严重不良事件,所有受试者对该操作的耐受性良好。虽然本研究并非设计用于确定疗效,也没有足够的效力,但接受较高光通量的受试者临床症状缓解时间显著缩短(p=0.028)。此外,接受较高光通量的受试者术后引流导管的引流量减少(ρ=-0.18),尽管这种差异不显著(p=0.43)。
MB-PDT是影像引导下经皮脓肿引流的一种安全可行的辅助方法。临床指标表明对PDT存在剂量依赖性反应,这促使未来开展2期研究评估MB-PDT在该患者群体中的疗效。