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Recruiting NCT04890171

Comparison of Endoscopic Resection and Surgery for Early Gastric Cancer With Undifferentiated Histological Type

No phase Interventional Stomach Cancer Undifferentiated Type Expanded Indication of Endoscopic Resection

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Endoscopic submucosal dissection, Surgery.
Who it may be relevant to
Registry conditions: Stomach Cancer, Undifferentiated Type, Expanded Indication of Endoscopic Resection. Basic parameters: 19 years — 75 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
South Korea
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

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

Overview

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.

Detailed description

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.

Interventions

  • Procedure Endoscopic submucosal dissection
    Endoscopic submucosal dissection by a endoscopist using endoscopic devices
  • Procedure Surgery
    Gastrectomy with lymph node dissection by a surgeon

Primary outcome measures

  • 3-year disease-free survival in the ITT population [Time frame: 3 years after the last participant enrollment]
Secondary outcome measures (6)
  • 3-year disease-free survival in the PP population [Time frame: 3 years after the last participant enrollment]
  • Overall survival [Time frame: 5 years after the last participant enrollment]
  • Curative resection rate of ESD [Time frame: 2 year after the participant enrollment]
  • Quality of life changes during follow-up periods [Time frame: 3 years after the last participant enrollment]
  • Treatment related complications (adverse events) [Time frame: 3 years after the last participant enrollment]
  • Cost-effectiveness measured with Incremental cost effective ratio (ICER) [Time frame: 3 years after the last participant enrollment]

Eligibility criteria

Inclusion criteria

  • 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

Exclusion criteria

  • 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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Treatment

Study locations

South Korea · 1 center
  • National Cancer Center, Korea — Goyang-si

Identifiers

NCT: NCT04890171 · NCC2021-0117

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗