Department of Gynecology and Obstetrics, Division of Reproductive Sciences & Women's Health Research, Johns Hopkins University School of Medicine, 720 Rutland Avenue, Ross Research Building, Room 624, Baltimore, MD, 21205, USA.
Department of Gynecology and Obstetrics, Minimally Invasive Gynecologic Surgeons, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Reprod Sci. 2021 Sep;28(9):2699-2709. doi: 10.1007/s43032-021-00573-8. Epub 2021 Apr 29.
Uterine fibroids feature excessive deposition of types I and III collagen. Previous ex vivo studies showed an FDA-approved collagenase (EN3835)-digested types I and III collagen fibers in fibroid tissues; however, collagenase had not been evaluated in vivo for effects on uterine fibroids. The objective was to assess the safety and tolerability of collagenase injection directly into uterine fibroids. This was a prospective, open label, dose escalation study. The study participants were fifteen women aged 35-50 years with symptomatic uterine fibroids planning to undergo hysterectomy. Three subjects received saline and methylene blue, three subjects received a fixed dose of EN3835, and 9 subjects received stepped, increasing dosages of EN3835, all by transvaginal, ultrasound-guided injections. Primary outcome measures were safety and tolerability of the injection and change in collagen content between treated and control tissues. There were no significant adverse events following injection of EN3835 into uterine fibroids. Masson's trichrome stains revealed a 39% reduction in collagen content in treated samples compared to controls (p <0.05). Second harmonic generation (SHG) analysis showed treated samples to have a 21% reduction in density of collagen compared to controls. Picrosirius-stained collagenase-treated fibroids showed collagen fibers to be shorter and less dense compared to controls. Subjects reported a decrease in fibroid-related pain on the McGill Pain Questionnaire after study drug injection in Group 2 at both 4-8 days and 60-90 days post-injection. The findings indicated that injection of collagenase was safe and well tolerated. These results support further clinical investigation of collagenase as a minimally invasive treatment of uterine fibroids. NCT0289848.
子宫肌瘤的特征是 I 型和 III 型胶原过度沉积。以前的离体研究表明,在纤维瘤组织中存在经美国食品和药物管理局批准的胶原酶(EN3835)消化的 I 型和 III 型胶原纤维;然而,胶原酶在体内对子宫肌瘤的作用尚未得到评估。本研究旨在评估胶原酶直接注射入子宫肌瘤的安全性和耐受性。这是一项前瞻性、开放标签、剂量递增研究。研究参与者为 15 名年龄在 35-50 岁之间、有症状的子宫肌瘤且计划接受子宫切除术的女性。3 名受试者接受生理盐水和亚甲蓝,3 名受试者接受固定剂量的 EN3835,9 名受试者接受递增剂量的 EN3835,均通过经阴道、超声引导下注射。主要观察指标为注射的安全性和耐受性以及治疗组织和对照组织之间胶原含量的变化。向子宫肌瘤内注射 EN3835 后无明显不良事件。Masson 三色染色显示,与对照组相比,治疗组的胶原含量减少了 39%(p <0.05)。二次谐波产生(SHG)分析显示,与对照组相比,治疗组的胶原密度降低了 21%。皮罗辛染色显示,胶原酶处理过的纤维瘤中的胶原纤维比对照组更短、更稀疏。在注射研究药物后 4-8 天和 60-90 天,第 2 组的受试者在 McGill 疼痛问卷中报告了与纤维瘤相关的疼痛减轻。研究结果表明,胶原酶注射是安全的,且耐受性良好。这些结果支持进一步对胶原酶作为子宫肌瘤微创治疗的临床研究。NCT0289848。