Indo-cyanine Green (ICG) in Paediatric Oncology MIS

Overview

Indo-cyanine green (ICG) is a dye that has been used for a variety of adult and paediatric uses since 1956. Over the past few years, near infrared (NIRF) technology has been developed which allow is use as a fluorescence agent during surgery. It has been used increasingly in the field of adult oncology surgery and has been shown to increase the efficacy of this surgery. The aim of this study is to evaluate the use of NIRF and ICG during specific minimally invasive surgery (MIS) procedures within paediatric oncology surgery. Their use will complement existing surgical techniques rather than replace them. Given the published advantages in adults this study aims to provide evidence of feasibility in the paediatric patients with cancer.

Full Title of Study: “An Open Label, Single Centre, Single Arm, Prospective Feasibility Study Evaluating the Effectiveness of Near-infrared Fluorescence (NIRF) Using Indo-cyanine Green (ICG) in Minimally Invasive Paediatric Oncology Surgery (MIS)”

Study Type

  • Study Type: Interventional
  • Study Design
    • Allocation: N/A
    • Intervention Model: Single Group Assignment
    • Primary Purpose: Treatment
    • Masking: None (Open Label)
  • Study Primary Completion Date: September 30, 2022

Detailed Description

The purpose of this study is to show the feasibility of using ICG in combination with NIRF and MIS in paediatric oncology surgery. It has been used increasingly over the past few years for a range of adult oncology surgical indications including tumour margin identification, lymph node identification and pulmonary metastectomy. It will be investigated in three groups of patients in our study: 1. Tumour margin identification-Identifying the margins of a tumour intra-operatively is crucial for many paediatric cancers. Incomplete resections or resections with involved margins often require upstaging of treatment with more intensive chemotherapy or radiotherapy. ICG will be injected intravenously and then NIRF will be used intermittently until fluorescence is achieved and an evaluation of the tumour and its margins will be performed. 2. Lymph node identification – It is standard of care for most oncology resections to remove lymph nodes that are suspected to be involved with tumour. Both SIOP and COG recommend the removal of 7 or more lymph nodes during a nephrectomy for Wilm's tumour although this is often not achieved. IGC will be injected directly into the tumour (or the adjacent tissue in 2-4 places) and then NIRF will be used intermittently until fluorescence is achieved. An evaluation of the tumour and any fluorescent lymph nodes will then take place and any fluorescent lymph nodes will be removed. 3. Pulmonary metastectomy – Many paediatric cancers including Wilm's tumour have a propensity to metastasise to the lungs. Removal of all lung metastases is important as it has the potential to down-stage tumours, obviating the need for pulmonary radiotherapy. Modern radiology techniques can identify lesions as small as 1mm which are often not palpable at the time of surgery. Relying on finger palpation requires patients to have a thoracotomy with all of the associated complications. ICG will be injected intravenously and then NIRF will be combined with MIS to identify any fluorescent lesions. The location of any lesions will be compared with those seen on pre-surgical imaging (current standard practice). For all three groups of patients, the use of ICG and NIRF will complement rather than replace existing surgical technique in patients who require surgery already. Data will be collected on the number of lesions which do/do not fluoresce as well as the histology of lesions removed. They will be separated into lesions which do not fluoresce, lesions which were removed before fluorescence (they will be checked for ex-vivo fluorescence) and fluorescing lesions so that the histological characteristics of each group can be compared.

Interventions

  • Drug: Indocyanine green
    • Intravenous or intraparenchymal injection

Arms, Groups and Cohorts

  • Experimental: Single Arm
    • Injection of Indocyanine Green at doses detailed on summary of product characteristics for each age range

Clinical Trial Outcome Measures

Primary Measures

  • Number of fluorescent nodes resected during minimally invasive tumour nephrectomy
    • Time Frame: Until the end of surgery, 2 hours
    • Number of fluorescent nodes resected per patient
  • Is Fluorescent guided tumour resection easier than non-fluorescent guided.
    • Time Frame: until the end of surgery, 2 hours
    • Subjective surgeon analysis of intra-operative conditions on a Likert scale per patient
  • To evaluate if NIRF and ICG allow detection of pulmonary metastases
    • Time Frame: until the end of surgery, 2 hours
    • Comparison of number of lesions seen on CT with those seen with fluoroscopy per patient

Secondary Measures

  • To evaluate if fluorescent nodes or metastases are more likely to contain viable tumour
    • Time Frame: until histopathology is reported, 2 weeks
    • Number of fluorescent nodes and metastases containing viable tumour per patient

Participating in This Clinical Trial

Inclusion Criteria

  • Age between 1 day and 15 years 365 days – Have a diagnosis of an intra-abdominal, retroperitoneal or intra-thoracic tumour or pulmonary metastases – Require surgery as part of their treatment – Tumour or metastasis suitable for MIS resection based on assessment of the pre-operative imaging Exclusion Criteria:

  • Allergic to ICG – Allergic to iodine or iodides – Due to receive radioactive iodine as part of a treatment – Hyperthyroidism – Unwilling to participate – Chronic Kidney Disease stage V

Gender Eligibility: All

Minimum Age: 1 Day

Maximum Age: 15 Years

Are Healthy Volunteers Accepted: No

Investigator Details

  • Lead Sponsor
    • Birmingham Women’s and Children’s NHS Foundation Trust
  • Provider of Information About this Clinical Study
    • Sponsor
  • Overall Official(s)
    • Max Pachl, Principal Investigator, Birmingham Women’s and Children’s NHS Foundation Trust

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