跳至主要内容
临床试验/NCT04890171
NCT04890171招募中不适用

Comparison of Endoscopic Resection and Surgery for Early Gastric Cancer With Undifferentiated Histological Type: a Multicenter Randomized Controlled Trial (ERASE-GC Trial)

National Cancer Center, Korea2 个研究点 分布在 1 个国家目标入组 708 人开始时间: 2021年6月11日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
708
试验地点
2
主要终点
3-year disease-free survival in the ITT population

研究概览

简要总结

This multi-center, randomized controlled trial is designed to evaluate clinical effectiveness and cost-effectiveness of ESD for undifferentiated type of EGC meeting the expanded indication compared with surgery.

详细描述

Endoscopic submucosal dissection (ESD) is a minimally invasive treatment of early gastric cancer (EGC). Because of the stomach preservation, ESD provides a better quality of life (QoL) in EGC patients than surgery. In addition, medical costs are lower in patients underwent ESD than in those underwent surgery. In 2018, gastric cancer management guidelines by the Korean Gastric Cancer Association and Japanese Gastric Cancer Association (JGCA) stated that undifferentiated type of EGC, clinically diagnosed as tumor confined to the mucosa without ulcer, and size ≤2 cm, is included in the expanded indication of ESD. In the 2018 JGCA guideline (version 5), ESD is an investigational treatment for patients with undifferentiated type of EGC meeting the expanded indication whereas surgery (gastrectomy with lymph node dissection) is a standard treatment. Previous single center retrospective studies reported favorable long-term outcomes of ESD for undifferentiated type EGC meeting the expanded criteria on final pathological evaluations compared with that of surgery. More recently, a multi-center retrospective cohort study including 18 Korean university hospitals also reported no significant difference in overall mortality between ESD and surgery after propensity score matching (hazard ratio [HR] for overall mortality in the ESD group, 2.36; 95% confidence interval [CI] 0.91-6.10; p=0.078) during a median follow-up of 75.6 months. However, gastric cancer recurrence occurred only in the ESD group, and the HR for gastric cancer recurrence in the ESD group was 25.49 (95% CI 1.32-491.27; p=0.032). The 3-year disease-free survival (DFS) rate including gastric cancer recurrence or death was 94.9% in the ESD group and 98.1% in the surgery group. Thus, surgery group had a better DFS than ESD group (p=0.002 by log-rank test), and the HR for gastric cancer recurrence or death in the surgery group compared with the ESD group was 0.26 (95% CI, 0.10-0.64; p=0.003). However, previous studies could provide only a low level of evidence because of study limitations including the retrospective study design and incomplete data of patient survival and gastric cancer recurrence during follow-up. The studies did not evaluate QoL and cost-effectiveness after ESD and surgery. Therefore, we designed a multi-center, randomized controlled trial to provide a high level of evidence for clinical effectiveness and cost-effectiveness of ESD for undifferentiated type of EGC meeting the expanded indication.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
19 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients who are diagnosed with undifferentiated type EGC (signet ring cell carcinoma, poorly differentiated tubular adenocarcinoma, or poorly cohesive carcinoma) that meets the expanded indication of ESD 1) Tumor confined to the mucosa without ulcer, and size ≤2 cm on endoscopic evaluations 2) No evidence of lymph node metastasis and distant metastasis on abdominal CT scan
  • Adult patients aged 19-75 years
  • Patients who had willingness to sign an informed consent form

排除标准

  • Patient age: < 19 years or age > 75 years
  • Diagnosis and active treatment for other organ cancer except carcinoma in situ and non-melanomatous skin cancer within 5 years
  • Previous gastrectomy or esophagectomy history
  • Multiple gastric cancers
  • Current treatment for serious medical condition which could hinder study participation including severe heart dysfunction, liver cirrhosis, renal failure, chronic obstructive pulmonary disease or asthma, or uncontrolled infection
  • Inability to provide an informed consent
  • Inadequate conditions for study enrollment according to the evaluation of study physicians

结局指标

主要结局

3-year disease-free survival in the ITT population

时间窗: 3 years after the last participant enrollment

Disease-free survival (gastric cancer recurrence or death from any causes)

次要结局

  • 3-year disease-free survival in the PP population(3 years after the last participant enrollment)
  • Overall survival(5 years after the last participant enrollment)
  • Quality of life changes during follow-up periods(3 years after the last participant enrollment)
  • Curative resection rate of ESD(2 year after the participant enrollment)
  • Treatment related complications (adverse events)(3 years after the last participant enrollment)
  • Cost-effectiveness measured with Incremental cost effective ratio (ICER)(3 years after the last participant enrollment)

研究者

申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

Il Ju Choi

Principal Scientist

National Cancer Center, Korea

研究点 (2)

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