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NCT Number: NCT07295002

Sentinel Node Resection With or Without LECS After Noncurative ESD for EGC

For patients with non-curative resection after endoscopic submucosal dissection (ESD) for early gastric cancer (EGC), complementary surgery is generally recommended. However, about 2/3 of patients have no remaining tumor in the stomach or regional lymph nodes. In this trial, Indocyanine Green (ICG)-guided lymphadenectomy with or without laparoscopic and endoscopic cooperative surgery (LECS) will be tested as a less invasive alternative in such cases. For patients with a primary radically resected EGC, ICG-guided lymphadenectomy alone will be performed. For patients with deep-margin positive EGC, ICG-guided lymphadenectomy and LECS will be performed, in order to ensure both local tumor control in the stomach and in regional nodes.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

About this study

Endoscopic submucosal dissection (ESD) is the recommended treatment for early gastric cancer (EGC) who are fullfillling the criteria based on international guidelines. After ESD, some resections are classified as non-curative because of factors such as non radicality (especially when the deep margin is positive for cancer), lymphovascular invasion or deep submucosal invasion Sm>1. In such cases, guidelines recommend complementary gastrectomy and lymphadenectomy. Gastrectomy is known to carry a risk for severe complications in about 9-22 % of cases. Furthermore, up to 2/3 of patients are found to have no remaining tumor in the stomach or regional nodes after surgery.

In this trial, Indocyanine Green (ICG)-guided lymphadenectomy including sentinel node resection, with or without complementary laparoscopic and endoscopic cooperative surgery (LECS) will be tested as a less invasive treatment option. For patients with radically resected EGC, ICG-guided lymphadenectomy alone will be performed. In patients with deep margin positive EGC, ICG-guided lymphadenectomy and LECS will be performed.

ICG-guided lymphadenectomy is performed by first injecting 100 times diluted ICG in four quadrants in the submucosa around the tumor scar with gastroscopy. After 15 minutes, the draining nodes will be visualized with laparoscopy, and locally resected. LECS is performed by endoscopic marking of the scar followed circumferential mucosal cutting, trimming, and perforation of the stomach followed by full-thickness resection of the scar with laparoscopy. After resection, the resected specimen will be taken out and the stomach defect sutured laparoscopically.

After the procedure, the patient will be presented at a multidisciplinary tumor board. If only clinical follow-up is recommended, the patient will be followed closely with gastroscopy and computer tomography (CT) scan every 3 months for the first year.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • EGC previously treated with ESD according to current guidelines (differentiated adenocarcinoma, not ulcerative, of any size, differentiated adenocarcinoma ulcerative </=3cm, undifferentiated adenocarcinoma not ulcerative </=2cm)
  • Non curative resection
  • Lymphovascular invasion
  • Non-radical resection vertical margin
  • deep submucosal invasion
  • Signed informed consent

Exclusion criteria

  • Location within 2 cm from cardia or pylorus
  • Non-curative resection with only non-radicality horizontal margin
  • Inoperative because of severe comorbidities
  • Previous radiotherapy to the upper abdomen
  • Pregnancy
  • Allergy to ICG
  • Inability to provide informed consent due to cognitive impairment, language barrier, or other reasons impairing understanding and autonomous decision-making.

Treatment and study plan

ICG-guided lymphadenectomy

Procedure

Submucosal injection of ICG in quadrants around the scar after ESD, followed by laparoscopic resection of positive lymph nodes after 15 minutes

Laparoscopic and endoscopic cooperative surgery (LECS)

Procedure

Endoscopic marking and submucosal cutting around the scar after ESD, followed by perforation of the gastric wall and laparoscopic full thickness resection of the area under endoscopic guidance.

Primary outcomes

  1. Severe complications defined as Clavien-Dindo >/= III

    Time frame: Periprocedural

    Safety of the procedure, defined as Clavien-Dindo complication grade >/= III

Secondary outcomes

  1. Any complications

    Time frame: Periprocedural

    Any complication during the procedure (Clavien-Dindo II-IV)

  2. Postoperative bleeding

    Time frame: Periprocedural

    Postoperative bleeding requiring blood transfusion

  3. Leakage

    Time frame: Periprocedural

    Leakage/postoperative abscess requiring drainage

  4. Operation time

    Time frame: Periprocedural

    Time of the surgical procedure

  5. Pathological tumor (T)-stage

    Time frame: Up to 2 months post procedure

    Depth of tumor invasion into the gastric wall (for LECS cases)

  6. Tumor-free resection margins

    Time frame: Up to 2 months post procedure

    The rate of horizontal and vertical margins free of tumor cells (for LECS cases).

  7. Number of lymph nodes

    Time frame: Periprocedural

    Number of lymph nodes harvested during the procedure

  8. Number of positive lymph nodes

    Time frame: Up to 2 months post procedure

    Number of lymph nodes positive for cancer

  9. Hospital-stay

    Time frame: From the day of the procedure until patient is discharged from the hospital, assessed up to 12 weeks post procedure

    Number of days from the procedure until discharge

  10. Health-related quality of life (HQL) score QLQ-30

    Time frame: Preoperatively, after 30 days and 1 year

    Pre and postoperative HQL, tested with the validated score QLQ-C30 (The EORTC QLG Core Questionnaire for cancer patients)

  11. Health-related quality of life (HQL) score OG25

    Time frame: Preoperatively, after 30 days and 1 year

    Pre and postoperative HQL, tested with the validated score OG25 (The EORTC QLG Module Questionnaire specifically for esophago-gastric patients)

  12. 30-day mortality

    Time frame: From procedure to maximum 30 days postoperatively

    30-day mortality

  13. In-hospital mortality

    Time frame: From the day of the procedure until patient is discharged from the hospital, assessed up to 12 weeks post procedure

    In-hospital mortality

  14. 1-year disease-free survival

    Time frame: Until 1 year after the procedure

    1-year disease-free survival

Study contacts

Contact information is provided by the study sponsor or research team.

Henrik Maltzman, MD

CONTACT

[email protected]

+46706334445

Ioannis Rouvelas, MD, PhD

CONTACT

[email protected]

+46707976814

Sponsors and collaborators

Lead sponsor

Region Stockholm

Other Gov

Registry information

Official study title

COmpletion Sentinel Node Resection With or Without Minimally invAsive and Endoscopic Cooperative Surgery Following noncuRative Endoscopic Submucosal Dissection for Early Gastric Cancer

Acronym: Co-SNARE

Important dates

Study start
2026
Primary completion
2029
Study completion
2029
First posted
Dec 19, 2025
Registry last updated
Dec 19, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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