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国际广泛子宫颈切除术评估:IRTA 研究。

International radical trachelectomy assessment: IRTA study.

机构信息

Department of Gynecologic Oncology and Reproductive Medicine, University of Texas MD Anderson Cancer Center, Houston, Texas, USA

Department of Gynecologic Oncology and Reproductive Medicine, University of Texas MD Anderson Cancer Center, Houston, Texas, USA.

出版信息

Int J Gynecol Cancer. 2019 Mar;29(3):635-638. doi: 10.1136/ijgc-2019-000273. Epub 2019 Feb 13.

Abstract

BACKGROUND

Radical trachelectomy is considered a viable option for fertility preservation in patients with low-risk, early-stage cervical cancer. Standard approaches include laparotomy or minimally invasive surgery when performing radical trachelectomy.

PRIMARY OBJECTIVE

To compare disease-free survival between patients with FIGO (2009) stage IA2 or IB1 (≤2cm) cervical cancer who underwent open versus minimally invasive (laparoscopic or robotic) radical trachelectomy.

STUDY HYPOTHESIS

We hypothesize that minimally invasive radical trachelectomy has similar oncologic outcomes to those of the open approach.

STUDY DESIGN

This is a collaborative, multi-institutional, international, retrospective study. Patients who underwent a radical trachelectomy and lymphadenectomy between January 1, 2005 and December 31, 2017 will be included. Institutional review board approval will be required. Each institution will be provided access to a study-specific REDCap (Research Electronic Data Capture) database maintained by MD Anderson Cancer Center and will be responsible for entering patient data.

INCLUSION CRITERIA

Patients with squamous, adenocarcinoma, or adenosquamous cervical cancer FIGO (2009) stages IA2 and IB1 (≤2 cm) will be included. Surgery performed by the open approach or minimally invasive approach (laparoscopy or robotics). Tumor size ≤2 cm, by physical examination, ultrasound, MRI, CT, or positron emission tomography (at least one should confirm a tumor size ≤2 cm). Centers must contribute at least 15 cases of radical trachelectomy (open, minimally invasive, or both).

EXCLUSION CRITERIA

Prior neoadjuvant chemotherapy or radiotherapy to the pelvis for cervical cancer at any time, prior lymphadenectomy, or pelvic retroperitoneal surgery, pregnant patients, aborted trachelectomy (intra-operative conversion to radical hysterectomy), or vaginal approach.

PRIMARY ENDPOINT

The primary endpoint is disease-free survival measured as the time from surgery until recurrence or death due to disease. To evaluate the primary objective, we will compare disease-free survival among patients with FIGO (2009) stage IA2 or IB1 (≤2cm) cervical cancer who underwent open versus minimally invasive radical trachelectomy.

SAMPLE SIZE

An estimated 535 patients will be included; 256 open and 279 minimally invasive radical trachelectomy. Previous studies have shown that recurrence rates in the open group range from 3.8% to 7.6%. Assuming that the 4.5-year disease-free survival rate for patients who underwent open surgery is 95.0%, we have 80% power to detect a 0.44 HR using α level 0.10. This corresponds to an 89.0% disease-free survival rate at 4.5 years in the minimally invasive group.

摘要

背景

根治性宫颈切除术被认为是低危、早期宫颈癌患者保留生育能力的一种可行选择。在进行根治性宫颈切除术时,标准方法包括剖腹手术或微创手术。

主要目的

比较 FIGO(2009)分期为 IA2 或 IB1(≤2cm)宫颈癌患者行开腹与微创(腹腔镜或机器人)根治性宫颈切除术的无病生存率。

研究假设

我们假设微创手术在肿瘤学方面的结果与开放手术相似。

研究设计

这是一项合作的、多机构的、国际性的、回顾性研究。将纳入 2005 年 1 月 1 日至 2017 年 12 月 31 日期间行根治性宫颈切除术和淋巴结切除术的患者。需要获得机构审查委员会的批准。每个机构都将可以访问由 MD 安德森癌症中心维护的特定于研究的 REDCap(研究电子数据捕获)数据库,并负责输入患者数据。

纳入标准

FIGO(2009)分期为 IA2 和 IB1(≤2cm)的宫颈癌患者,包括鳞癌、腺癌或腺鳞癌。手术方式为开腹或微创手术(腹腔镜或机器人)。肿瘤大小≤2cm,通过体格检查、超声、MRI、CT 或正电子发射断层扫描(至少一种应确认肿瘤大小≤2cm)。中心至少要贡献 15 例根治性宫颈切除术(开腹、微创或两者兼有)。

排除标准

宫颈癌在任何时候的盆腔新辅助化疗或放疗、先前的淋巴结切除术或盆腔后腹膜手术、孕妇、流产的宫颈切除术(术中转为根治性子宫切除术)或阴道入路。

主要终点

无病生存率是从手术到复发或因疾病死亡的时间,是主要终点。为了评估主要目标,我们将比较 FIGO(2009)分期为 IA2 或 IB1(≤2cm)宫颈癌患者行开腹与微创根治性宫颈切除术的无病生存率。

样本量

预计将纳入 535 例患者;开腹 256 例,微创 279 例。先前的研究表明,开腹组的复发率为 3.8%至 7.6%。假设行开腹手术的患者 4.5 年无病生存率为 95.0%,我们有 80%的把握力用α水平 0.10 检测到 0.44 的 HR。这相当于微创组 4.5 年无病生存率为 89.0%。

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