Department of Gynecology, Cervical Cancer Center, European Institute of Oncology, Milan, Italy.
Gynecol Oncol. 2013 Jul;130(1):69-74. doi: 10.1016/j.ygyno.2013.02.038. Epub 2013 Mar 6.
The aim of the study is to evaluate the response to neoadjuvant chemotherapy (NACHT) of patients with recurrent cervical cancer who were poor candidates for pelvic exenteration (PE), and the impact on DFS and OS.
A retrospective data collection extracted from medical records of 61 patients submitted to pelvic exenteration was performed: 30 underwent up-front exenterative procedure whereas 31 received NACHT.
The median tumor size was significantly (P=0.0006) larger in the NACHT group compared to the up-front PE one (43.9 mm vs 28 mm), and a significant (P=0.04) higher percentage of patients (45 vs 20%) had lateral pelvic wall invasion in the NACHT group. No statistically significant difference in early and late complications was observed in the two groups. Median overall survival in study population was 42.9 months (95% CI: 22.2, 180.8). Median overall survival times as well as recurrence free survival times were not significantly different between NACHT (42.9 months and 36.1 months for OS and DFS respectively) vs. No NACHT (111.9 months and 48.1 months for OS and DFS respectively). There was an overall significant difference in DFS between negative and positive margins but the curves were similar for NACHT and up-front PE groups stratified by resection margin status.
In our series, though small and retrospective, NACHT prior to PE represents a feasible therapeutic option without intra-operative and early post-operative mortality or worsening of early and late complication rate and with acceptable long-term survival and DFS for recurrent cervical cancer patients who are poor candidates for up-front pelvic exenteration.
本研究旨在评估不适合盆腔切除术(PE)的复发性宫颈癌患者接受新辅助化疗(NACHT)的反应,以及对DFS 和 OS 的影响。
回顾性收集了 61 例接受盆腔切除术的患者的病历资料,其中 30 例患者行 upfront 切除术,31 例患者接受 NACHT。
与 upfront PE 组相比,NACHT 组的肿瘤大小中位数明显更大(P=0.0006)(43.9mm 对 28mm),且 NACHT 组有更高比例的患者(45%对 20%)存在侧盆壁侵犯。两组患者的早期和晚期并发症无统计学差异。研究人群的中位总生存期为 42.9 个月(95%CI:22.2,180.8)。NACHT 组(OS 和 DFS 分别为 42.9 个月和 36.1 个月)与无 NACHT 组(OS 和 DFS 分别为 111.9 个月和 48.1 个月)的中位总生存时间和无复发生存时间无显著差异。阴性和阳性切缘之间的 DFS 总体差异有统计学意义,但根据切缘状态分层后,NACHT 和 upfront PE 两组的曲线相似。
在我们的系列研究中,尽管规模较小且为回顾性研究,但在不增加术中及术后早期死亡率或增加早期及晚期并发症发生率的情况下,NACHT 先于 PE 是一种可行的治疗选择,对于不适合 upfront PE 的复发性宫颈癌患者具有可接受的长期生存和 DFS。