Department of Radiooncology, Medical Faculty of the University of Cologne, Cologne, Germany
Gynecologic Oncology Department, Hospital Erasto Gaertner, Curitiba, Brazil.
Int J Gynecol Cancer. 2020 Dec;30(12):1855-1861. doi: 10.1136/ijgc-2020-001973.
Revised staging of patients with locally advanced cervical cancer is based on clinical examination, imaging, and potential surgical findings. A known limitation of imaging techniques is an appreciable rate of understaging. In contrast, surgical staging may provide more accurate information on lymph node involvement. The aim of this prospective study was to evaluate the impact of pre-treatment surgical staging, including removal of bulky lymph nodes, on disease-free survival in patients with locally advanced cervical cancer.
Uterus-11 was a prospective international multicenter study including patients with locally advanced cervical cancer who were randomized 1:1 to surgical staging (experimental arm) or clinical staging (control arm) followed by primary platinum-based chemoradiation. Patients with histologically proven squamous cell carcinoma, adenocarcinoma, or adenosquamous cancer International Federation of Gynecology and Obstetrics (FIGO) 2009 stage IIB-IVA underwent gynecologic examination and pre-treatment imaging including abdominal computed tomography (CT) and/or abdominal magnetic resonance imaging (MRI). Patients had chest imaging (any of the following: X-ray, CT, or PET-CT). The primary endpoint was disease-free survival and the secondary endpoint was overall survival. An ad hoc analysis was performed after trial completion for cancer-specific survival. Randomization was conducted from February 2009 to August 2013.
A total of 255 patients (surgical arm, n=130; clinical arm, n=125) with locally advanced cervical cancer were randomized. Of these, 240 patients were eligible for analysis. The two groups were comparable with respect to patient characteristics. The surgical approach was transperitoneal laparoscopy in most patients (96.6%). Laparoscopic staging led to upstaging in 39 of 120 (33%) patients. After a median follow-up of 90 months (range 1-123) in both arms, there was no difference in disease-free survival between the groups (p=0.084). For patients with FIGO stage IIB, surgical staging is superior to clinical staging with respect to disease-free survival (HR 0.51, 95% CI 0.30 to 0.86, p=0.011). In the post-hoc analysis, surgical staging was associated with better cancer-specific survival (HR 0.61, 95% CI 0.40 to 0.93, p=0.020).
Our study did not show a difference in disease-free survival between surgical and clinical staging in patients with locally advanced cervical cancer. There was a significant benefit in disease-free survival for patients with FIGO stage IIB and, in a post-hoc analysis, a cancer-specific survival benefit in favor of laparoscopic staging. The high risk of distant metastases in both arms emphasizes the need for further evaluation.
局部晚期宫颈癌患者的修订分期基于临床检查、影像学和潜在的手术发现。影像学技术的一个已知局限性是存在相当高的分期不足率。相比之下,手术分期可能提供关于淋巴结受累的更准确信息。本前瞻性研究的目的是评估术前手术分期(包括切除大体积的淋巴结)对局部晚期宫颈癌患者无病生存率的影响。
Uterus-11 是一项国际多中心前瞻性研究,纳入了局部晚期宫颈癌患者,他们被随机分为 1:1 接受手术分期(实验组)或临床分期(对照组),然后接受以铂类为基础的同期放化疗。组织学证实为鳞癌、腺癌或腺鳞癌的国际妇产科联合会(FIGO)2009 分期 IIB-IVA 期患者接受妇科检查和术前影像学检查,包括腹部计算机断层扫描(CT)和/或腹部磁共振成像(MRI)。所有患者均行胸部影像学检查(以下任意一种:X 射线、CT 或 PET-CT)。主要终点为无病生存率,次要终点为总生存率。试验完成后进行了癌症特异性生存率的分析。从 2009 年 2 月至 2013 年 8 月进行随机分组。
共有 255 例局部晚期宫颈癌患者(手术组 n=130;临床组 n=125)被随机分组。其中,240 例患者符合分析条件。两组患者的特征具有可比性。大多数患者采用经腹腹腔镜(96.6%)进行手术分期。腹腔镜分期使 120 例患者中的 39 例(33%)分期升高。两组患者中位随访时间均为 90 个月(范围 1-123),无病生存率无差异(p=0.084)。对于 FIGO 分期为 IIB 的患者,手术分期的无病生存率优于临床分期(HR 0.51,95%CI 0.30 至 0.86,p=0.011)。在事后分析中,手术分期与更好的癌症特异性生存率相关(HR 0.61,95%CI 0.40 至 0.93,p=0.020)。
本研究未显示局部晚期宫颈癌患者手术与临床分期之间无病生存率存在差异。FIGO 分期为 IIB 的患者无病生存率显著提高,且在事后分析中腹腔镜分期具有癌症特异性生存优势。两组患者的远处转移风险均较高,这强调了进一步评估的必要性。