Fluorescence-guided Resection Of Colorectal Liver Metastases Using SGM-101 and Indocyanine GREEN

Trial Title: Fluorescence-guided Resection Of Colorectal Liver Metastases Using SGM-101 and Indocyanine GREEN

NCT ID: NCT05965817

Condition: Colorectal Cancer
Liver Metastasis Colon Cancer
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Conditions: Official terms:
Neoplasm Metastasis
Liver Neoplasms

Study type: Interventional

Study phase: Phase 2

Overall status: Recruiting

Study design:

Allocation: N/A

Intervention model: Single Group Assignment

Intervention model description: In total 10 patients will be included who are scheduled for resection of colorectal liver metastases and meet at least one of the following criteria: 1. Scheduled for resection of >3 CRLM or, 2. Completed neo-adjuvant chemotherapy, of which the last course was completed within 3 months before surgery or, 3. Scheduled for surgery because of a locally recurrent liver metastasis.

Primary purpose: Diagnostic

Masking: None (Open Label)

Intervention:

Intervention type: Drug
Intervention name: SGM-101 op top of ICG
Description: SGM-101 op top of ICG
Arm group label: Patients with colorectal liver metastases receiving SGM-101 and ICG

Summary: This will be the first trial testing the feasibility of working simultaneously with the two fluorescent dyes ICG and SGM-101 in 10 patients with colorectal metastases.

Detailed description: 25-30% of patients with colorectal cancer develop colorectal liver metastases (CRLM). Cornerstone for optimal survival is achieving radical surgical resections of all metastases . To assist the surgeon in achieving this, the use of intra-operative ICG for fluorescent tumour delineation has widely been adopted as standard of care. Multiple international trials have demonstrated that the use of ICG increases the rate of radical resections and result in the detection of additional malignant lesions invisible to the naked eye. However, the rate of false positives is still high and although it has increased the number of radical resections, even in a minimal invasive cohort the unintended R1 rate is still as much as 8%. Therefore, there is a need of an additional real-time intra-operative tool to detect R1 resections, especially in patients with a priori high risk for R1. To illustrate, in a large shared database of the Erasmus University Medical Center was found that patients that either received neoadjuvant chemotherapy, underwent a resection for >3 CRLM or patients that had a locally recurrent liver metastasis were independently associated with high R1 rates, ranging between 23-29%. Therefore, here is proposed the addition of SGM-101, a tumour targeted (carcinoembryonic antigen, CEA) NIR-fluorescence probe to ICG in patients scheduled for a resection with high risk of R1, ultimately to reduce the R1 ratio. This is the first trial testing the feasibility of working simultaneously with the two fluorescent dyes. If feasibility is met in this trial, this is a step-up towards a powered trial with primary objective to reduce the rate of R1 resections. An additional exploratory objective of this study is to investigate the feasibility of SGM-101's potential to isolate circulating tumour cells (CTCs) and tumour-derived extracellular vesicles (EVs) as biomarkers for CRC. The load of CTCs and EVs in the circulation is strongly associated with poor clinical outcomes. Studies have shown that they contain information about the molecular profile of the tumour. The administration of SGM-101 may enable the detection of CEA positive CTCs and EVs.

Criteria for eligibility:
Criteria:
Inclusion Criteria: - In order to be eligible to participate in this study, a subject must meet all of the following criteria: 1. Diagnosed with liver metastases of colorectal origin for which surgical resection is proposed and meet at least one of the following criteria: 1. Scheduled for surgical resection of >3 CRLM or; 2. completed neo-adjuvant therapy, of which the last course was completed within 3 months before surgery or; 3. Scheduled for surgery because of a locally recurrent liver metastasis. 2. ≥18 years old. 3. Willing and capable to give informed consent before study specific procedures Exclusion Criteria: - A potential subject who meets any of the following criteria will be excluded from participation in this study: 1. Patients with contraindications for SGM-101 1. History of any anaphylactic shock; 2. Patients pregnant or breastfeeding (pregnancy should be ruled out by a pregnancy test within two weeks prior to administration of the conjugate); 3. Known positive test for human immunodeficiency virus (HIV), hepatitis B surface antigen (HBsAG) or hepatitis C virus (HCV) antibody or patients with untreated serious infections; 4. Previous administration of SGM-101 2. Patients with contraindications for Indocyanine green: 1. Allergy for shells and/or clamps 2. Hyperthyroidism 3. Known allergy for ICG 3. Any condition that the investigator considers to be potentially jeopardizing the patient's well-being or the study objectives

Gender: All

Minimum age: 18 Years

Maximum age: N/A

Healthy volunteers: No

Locations:

Facility:
Name: Leiden University Medical Center

Address:
City: Leiden
Zip: 2333ZA
Country: Netherlands

Status: Recruiting

Contact:
Last name: Mats Warmerdam, Msc

Phone: +31715298420
Email: m.i.warmerdam@lumc.nl

Start date: December 1, 2023

Completion date: May 1, 2025

Lead sponsor:
Agency: Leiden University Medical Center
Agency class: Other

Source: Leiden University Medical Center

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT05965817