Detection of Upper Gastrointestinal Tumour Depth and Demarcation Using Systemic Administration of Indocyanine Green During Endoscopic Submucosal Dissection

Trial statusRecruiting
Trial phasePhase 1, Phase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity Medical Center Groningen

About this trial

Endoscopic submucosal dissection (ESD) is a relatively new technique to treat superficial cancers in the upper gastrointestinal (GI) tract. Previous studies reported high en bloc resection rates (95%-97%). However, R0 resection rates (84.5%) suggest that the tumour is not radically removed in all cases, resulting in a risk of tumour recurrence. One of the key challenges is the limited accuracy in determining the depth of cancer invasion. To reduce the risk of tumour recurrence, the endoscopist would greatly benefit from proper and complete visualization of the tumour margin and depth during ESD. Several studies have shown that near-infrared quantified fluorescence molecular endoscopy (qFME) could serve as a red flag detection method and might be a useful imaging tool for tumour demarcation in the upper GI tract. The aim of this study is to evaluate the feasibility of ICG-enhanced near-infrared qFME to determine tumour demarcation and tumour depth in upper GI tumours (e.g. superficial esophageal and/or gastric adenocarcinoma (T1)) during ESD.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients with confirmed superficial esophageal and/or gastric adenocarcinoma (T1) and are scheduled for ESD within the UMCG;

Age of 18 years or older;

Able to provide written informed consent.

Disqualifiers

Known allergy to indocyanine green;

Known allergies to iodine, shellfish and/or clams;

eGFR < 30 mL/min/1.73 m2;

Pregnancy or breastfeeding;

Trial design

Design model

Single group

Treatments tested in this trial

  • Indocyanine Green (IC-Green)

    Drug

    Systemic administration of indocyanine green during the endoscopic procedure.

  • Fluorescence guided identification using indocyanine green

    Diagnostic test

    Near-infrared quantified fluorescence molecular endoscopy (qFME) will be used during the endoscopic procedure.

Treatment groups

10 Participants
are divided into 1 treatment group
Group A: Systemic administration of ICGExperimental treatment 2 interventions

Trial outcomes

Primary outcomes

1

Feasibility of ICG-enhanced qFME to determine tumour demarcation and depth in upper gastrointestinal tumours during ESD

Feasibility will be assessed by analyzing the fluorescent imaging data obtained during and after the procedure. Visible fluorescence will be determined by calculating the target-to-background ratio (TBR), where the target is defined as the mean pixel intensity of the resection bed in areas displaying fluorescence.

Time frame
One week after the qFME procedure
2

Feasibility of ICG-enhanced qFME to determine tumour demarcation and depth in upper gastrointestinal tumours during ESD

Secondary evaluation will focus on whether visible fluorescence after resection correlates with an R1 resection grade based on histopathology.

Time frame
One week after the qFME procedure
3

Feasibility of ICG-enhanced qFME to determine tumour demarcation and depth in upper gastrointestinal tumours during ESD

Fluorescence will also be quantified using mucosal multi-diameter single-fiber reflectance / single-fiber fluorescence (MDSFR/SFF) spectroscopy, a non-invasive measurement technique.

Time frame
After study completion, to be expected within 8 months

Secondary outcomes

1

Visibility of the papilla of Vater and the intraduodenal part of the extrahepatic biliary anatomy by detecting fluorescent signal with ICG-enhanced qFME

Visibility is determined visual evaluation during the endoscopic procedure and calculating the TBR in the same manner as explained above.

Time frame
One week after the qFME procedure

Other outcomes

Sponsors and contacts

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