Department of Obstetrics & Gynecology, Gynecologic Oncology and Minimally Invasive Pelvic Surgery, IRCCS Ospedale Sacro Cuore Don Calabria, Negrar, Italy.
Department of Women's and Children's Health, Gynecology and Obstetrics Clinic, University of Padua, Padova, Italy.
Gynecol Endocrinol. 2021 Oct;37(10):930-933. doi: 10.1080/09513590.2021.1929151. Epub 2021 May 26.
The recurrence of deep infiltrating endometriosis (DIE) after its surgical excision is a big problem: postoperative treatment is crucial.
To compare two postoperative treatments: Dienogest and GnRH agonists.
Prospective Randomized Controlled Trial (RCT).
146 women submitted to laparoscopic eradication of DIE with bowel and parametrial surgery.
Patients were randomized into two groups. Group A ( = 81) received Triptorelin or Leuprorelin 3.75 mg every 4 weeks for 6 months. Group B ( = 65) received Dienogest 2 mg/day for at least 6 months. A first interview made after six months valued compliance to therapy, treatment tolerability, pain improvement, and side effects. A second interview at 30 ± 6 months valued pain relapse, imaging relapse, and pregnancy rate.
The primary outcome was to demonstrate the non-inferiority of Dienogest about the reduction in pain recurrence. Secondary outcomes were differences in terms of treatment tolerability, side effects, imaging relapse rate, and pregnancy rate.
Both Dienogest and GnRH agonists were associated with a highly significant reduction of pain at 6 and 30 months, without any significant difference ( < .001). About treatment tolerability, a more satisfactory profile was reported with Dienogest ( = .026). No difference in terms of clinical relapse, imaging relapse, and live births was found.
Dienogest has proven to be as effective as GnRH agonists in preventing recurrence of DIE and associated pelvic pain after surgery. Also, it is better tolerated by patients.
深部浸润型子宫内膜异位症(DIE)切除术后的复发是一个大问题:术后治疗至关重要。
比较两种术后治疗方法:地诺孕素和 GnRH 激动剂。
前瞻性随机对照试验(RCT)。
146 名接受腹腔镜 DIE 切除术和肠和附件手术的女性。
患者随机分为两组。A 组(n=81)接受曲普瑞林或亮丙瑞林 3.75mg,每 4 周一次,共 6 个月。B 组(n=65)接受地诺孕素 2mg/天,至少 6 个月。6 个月后进行第一次访谈,评估治疗依从性、治疗耐受性、疼痛改善和副作用。在 30±6 个月时进行第二次访谈,评估疼痛复发、影像学复发和妊娠率。
主要结局是证明地诺孕素在减少疼痛复发方面不劣于 GnRH 激动剂。次要结局是治疗耐受性、副作用、影像学复发率和妊娠率的差异。
地诺孕素和 GnRH 激动剂均与疼痛在 6 个月和 30 个月时的显著降低相关,无显著差异(<0.001)。关于治疗耐受性,地诺孕素的报告更令人满意(=0.026)。未发现临床复发、影像学复发和活产率的差异。
地诺孕素在预防手术后 DIE 复发和相关盆腔疼痛方面已被证明与 GnRH 激动剂同样有效。此外,它的耐受性更好。