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NCT Number: NCT04798898

Improving Survival of COlorectal LIver Metastases by RFA-mediated Immunostimulation

To examine radio frequency ablation as a treatment supplement to stimulate immunogenicity and improve survival for patients undergoing curative-intent surgery for colorectal liver metastases.

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Key information

Age range

18 year–99 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Aarhus University Hospital, Department of Surgery

Aarhus, 8200, Denmark

Location status: Recruiting

Location contact

Andrea Lund, MD

SUB_INVESTIGATOR

Frank V Mortensen, MD, DMSc

PRINCIPAL_INVESTIGATOR

Jakob Kirkegård, MD, PhD

CONTACT

[email protected]

Jakob Kirkegård, MD, PhD

SUB_INVESTIGATOR

About this study

PURPOSE:

To investigate the impact of immunostimulation using radio frequency ablation (RFA) on survival in patients undergoing curative-intent surgery for colorectal liver metastases (CRLM).

HYPOTHESIS:

RFA-mediated partial destruction of CRLM will stimulate the immune system to recognize otherwise hidden cancer antigens, which in turn will improve survival by inhibiting micrometastases and recurrence.

BACKGROUND:

CRLM affects around 1,600 individuals in Denmark each year. State-of-the-art treatment includes liver resection, RFA treatment, radiation therapy, and chemotherapy. Of all individuals undergoing surgery, 50% will experience local or distant recurrence of the disease within five years. Although liver resection is the gold standard, RFA treatment has evolved considerably in recent years. RFA is a parenchymal-sparing treatment for hepatic malignancies, inducing a localized coagulation necrosis of the tumor. This leads to release of tumor antigens, which activates the patients' immune system. However, many cancer cells, including those from CRLM, have the ability to hide their antigens to the patients' immune systems. Using RFA as immunostimulation prior to surgery, these antigens may become visible to the immune system, which in turn can help eradicating all tumor cells and decrease the risk of tumor recurrence. Combined, this likely improves survival.

METHODS:

220 patients with CRLM planned for surgery will be enrolled in this study. Patients will be randomized to +/- RFA treatment before surgery. Under guidance of ultrasonography, a single-electrode RFA-needle is placed in a CRLM with a diameter of at least 3 cm, which is later going to be resected. In 20 of the patients, we will draw blood samples for determination of immune status both pre- and postoperatively. All patients will be part of a work-up with regular CT-scans.

ENDPOINTS:

Disease free survival and overall survival. Secondarily, we will examine the effect of RFA treatment of tumors on the innate and adaptive immune system in 20 patients

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patients with colorectal liver metastases planned for resection
  • At least one tumor size >=3cm
  • Performance status 0-1

Exclusion criteria

  • Liver cirrhosis
  • Extrahepatic metastases that can not be addressed curatively
  • Other malignant diseases within 5 years prior to diagnosis
  • Prior RFA treatment

Treatment and study plan

RFA (radiofrequency ablation)

Device

Preoperative RFA-induced partial necrosis of the liver metastasis

Primary outcomes

  1. Overall survival

    Time frame: 3 years

    Median survival in each arm

Secondary outcomes

  1. One-year survival

    Time frame: 1 year

    One-year survival in each arm

  2. Two-year survival

    Time frame: 2 years

    Two-year survival in each arm

  3. Three-year survival

    Time frame: 3 years

    Three-year survival in each arm

  4. Recurrence rate

    Time frame: 1, 2, and 3 years

    Recurrence rate at 1, 2, and 3 years follow-up

Other outcomes

  1. Complications

    Time frame: 30-day postoperatively

    Immediate postoperative complications (bleeding, surgical site infection, intraabdominal abscesses, bile leak)

Study contacts

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

Jakob Kirkegård, MD, PhD

CONTACT

[email protected]

+4524995027

Sponsors and collaborators

Lead sponsor

University of Aarhus

Other

Collaborators

  • Aarhus University Hospital
  • Rigshospitalet, Denmark

Registry information

Acronym: ISCOLIM

Important dates

Study start
2022
Primary completion
2025
Study completion
2026
First posted
Mar 15, 2021
Registry last updated
Dec 5, 2024

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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