Division of Gynecologic Oncology, Fondazione Policlinico Universitario A. Gemelli, IRCCS, Rome, Italy.
Division of Gynecologic Oncology, Fondazione Policlinico Universitario A. Gemelli, IRCCS, Rome, Italy; Division of Gynecologic Oncology, Università Cattolica del Sacro Cuore, Rome, Italy.
Eur J Surg Oncol. 2018 Oct;44(10):1568-1572. doi: 10.1016/j.ejso.2018.08.006. Epub 2018 Aug 17.
to assess the feasibility of minimally invasive surgery in the management of lymph-nodal recurrences of gynecological cancers, in terms of surgical and oncological outcomes.
we retrospectively collected patients with isolated lymph-nodal recurrent disease of gynecological malignancies who underwent to minimally invasive lymphadenectomy at Catholic University of the Sacred Hearth in Rome (Italy), from January 2013 to November 2017.
Forty patients were considered eligible (31 LPS, 9 Robot); 24 (60.0%) with an ovarian cancer, 8 (20.0%) with a cervical cancer and 8 (20.0%) with an endometrial cancer recurrence. The most frequent site of lymph-nodal recurrence was represented by the aortic region (47.5%), while 18 patients (45.0%) experiencing pelvic lymph-nodal recurrence, 2 (5.0%) both pelvic and aortic relapse, and only 1 (2.5%) had an hepato-celiac lymph node recurrence. No patient required a laparotomic conversion. Median operative time was 220 min, median EBL was 80 mL, and median post-operative hospital stay was 2 days. There were 2 (5.0%) intra-operative and 4 (10.0%) post-operative complications, of which 2 were grade 3. The median follow-up was 22.5 months, and during this time 15 patients showed another relapse with a median time to progression of 12 months. Seven women died because of the disease. The 2-year post-relapse disease-free survival (PR-DFS) was 54.7%, and the 2-year post-relapse overall survival (PR-OS) was 79.3%.
In our experience minimally invasive surgery is a valid therapeutic approach in very select patients with localized lymph-nodal recurrence of gynecological cancers, with benefits about peri and post-operative morbidities and without compromising their oncological outcome.
评估微创外科治疗妇科恶性肿瘤淋巴结复发的可行性,从手术和肿瘤学结果方面评估。
我们回顾性收集了 2013 年 1 月至 2017 年 11 月在罗马天主教圣心大学接受微创淋巴结切除术的妇科恶性肿瘤孤立性淋巴结复发患者。
40 名患者符合条件(31 例 LPS,9 例机器人);24 例(60.0%)为卵巢癌,8 例(20.0%)为宫颈癌,8 例(20.0%)为子宫内膜癌复发。淋巴结复发最常见的部位是主动脉区(47.5%),18 例(45.0%)为盆腔淋巴结复发,2 例(5.0%)为盆腔和主动脉复发,仅 1 例(2.5%)为肝门淋巴结复发。无患者需要转为剖腹手术。中位手术时间为 220 分钟,中位出血量为 80 毫升,中位术后住院时间为 2 天。术中发生 2 例(5.0%)并发症,术后发生 4 例(10.0%)并发症,其中 2 例为 3 级。中位随访时间为 22.5 个月,在此期间 15 例患者出现另一次复发,中位无进展时间为 12 个月。7 名妇女因疾病死亡。2 年复发无病生存率(PR-DFS)为 54.7%,2 年复发总生存率(PR-OS)为 79.3%。
在我们的经验中,微创外科是妇科恶性肿瘤局限性淋巴结复发非常特殊患者的一种有效治疗方法,可减少围手术期和术后并发症,而不会影响肿瘤学结果。