Fluorescence Guided Laparoscopic-Endoscopic Cooperative Sentinel Lymph Node Navigation Surgery Strategy for Early Gastric Cancer(IDEAL Stage 2b)

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-80
SponsorBeijing Friendship Hospital

About this trial

The main treatment for early gastric cancer (EGC) include endoscopic submucosal dissection (ESD) and radical gastrectomy. However, appropriate treatment for patients who exceed the absolute indications and noncurative resection of ESD remains unestablished. Sentinel node navigation surgery (SNNS) enables limited lymph node resection, thereby facilitating function-preserving gastrectomy (FPG) and improving quality of life (QoL). SNNS seems to be the promising solution according to previous study, however evidence-based medicine was lacking. It is imperative to establish its safety and efficacy in patients with EGC. However, the optimal implementation of FPG remain unclear. Moreover, objective assessment of postoperative functional outcomes,remains limited.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

1) Patients aged 18-80 years, regardless of gender. 2) Patients with Eastern Cooperative Oncology Group (ECOG) score ≤ 2 and American Society of Anesthesiologists (ASA) score ≤ 2 who are candidates for a curative D2 gastrectomy.

Disqualifiers

1) Patients with a contraindication for gastroscopy. 2) Patients with uncontrollable diseases, such as coagulation disorders, epilepsy, central nervous system diseases or mental disorders, cardiopulmonary insufficiency, unstable angina, myocardial infarction, a cerebrovascular accident that occurred within 6 months, and other surgical contraindications.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Fluorescence Guided Laparoscopic-Endoscopic Cooperative Sentinel Lymph Node Navigation Surgery

    Procedure/Surgery

    Patients without prior ESD received ESD with laparoscopic sentinel basin dissection (LSBD) for ESD resectable lesions, otherwise patients received laparoscopic-endoscopic cooperative regional gastrectomy (LRG) with LSBD. For patients with prior non-curative ESD, LSBD alone was performed if margins were negative, otherwise LRG with LSBD was conducted. Intraoperative frozen-section pathological examination of the horizontal resection margin of the ESD or full-thickness specimen. During laparoscopic sentinel node basin dissection (LSBD), indocyanine green (ICG) (2 mL, 2.5 mg/mL) was endoscopically injected into the submucosal layer at four quadrants around the marking points (0.5 mL per quadrant). Fifteen minutes after ICG injection, sentinel lymph node basins (SLBs) were defined as the area within a 2 cm margin of the detected fluorescence stained nodes, which were marked with laparoscopic clips.

  • Laparoscopic D2 radical gastrectomy

    Procedure/Surgery

    Preparation: The patient is positioned supine with general anesthesia. An orogastric tube and Foley catheter are inserted. Antibiotics are administered, and sequential stockings are applied. Port Placement: Pneumoperitoneum is created via a Veress needle at the umbilicus. Working ports are placed in the upper quadrants, with a fifth port for liver retraction. Abdominal Exploration: The abdomen is inspected for metastases, and peritoneal cytology is performed. Dissection and Lymph Node Removal: The lesser omentum is divided near the liver, reaching the cardia and diaphragm. The gastrocolic ligament is divided along the transverse colon. Lymph node dissection begins along the splenic artery, then proceeds to the left gastric artery and celiac nodes. The left gastric vessels are controlled with endoclips.After lymph node dissection, distal subtotal gastrectomy is performed. Digestive tract reconstruction is typically done through a mini-laparotomy.

Treatment groups

312 Participants
are divided into 2 treatment groups
Group A: Fluorescence Guided Laparoscopic-Endoscopic Cooperative Sentinel Lymph Node Navigation Surgery StratExperimental treatment 1 intervention
Group B: D2 gastrectomyActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

3-year disease-free survival (DFS) rate

DFS is defined as the time from the date of surgery to the date of first documented tumor recurrence, metastasis, or death from any cause.

Time frame
From date of surgery to up to 3 years post-surgery

Secondary outcomes

1

5-year disease-free survival (DFS) rate

DFS is defined as the time from the date of surgery to the date of first documented tumor recurrence, metastasis, or death from any cause.

Time frame
From date of surgery to up to 5 years post-surgery
2

3-year overall survival (OS) rate

OS is defined as the time from the date of surgery to death from any cause.

Time frame
From date of surgery to up to 3 years post-surgery
3

5-year overall survival (OS) rate

OS is defined as the time from the date of surgery to death from any cause.

Time frame
From date of surgery to up to 5 years post-surgery
4

3-year recurrence-free survival (RFS) rate

RFS is defined as the time from the date of surgery to the first occurrence of disease recurrence.

Time frame
From date of surgery to up to 3 years post-surgery

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Beijing Friendship Hospital

Lead sponsor

China-Japan Friendship Hospital

Collaborator

Cancer Hospital Chinese Academy of Medical Scienc

Collaborator