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NCT Number: NCT06821958

Amplitude-modulated Radiofrequency Electromagnetic Field Treatment for Advanced Hepatocellular Carcinoma (Immune-RF)

Combined double immune checkpoint inhibition and radiofrequency electromagnetic field treatment for patients with advanced hepatocellular carcinoma

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Charité University Medicine Berlin

Berlin, 13353, Germany

Location status: Recruiting

Location contact

Pirus Ghadjar, Prof. Dr.

PRINCIPAL_INVESTIGATOR

Raphael Mohr, Dr.

PRINCIPAL_INVESTIGATOR

Yvonne Saewe

CONTACT

[email protected]

+49 30 450 527318

About this study

Charité University Medicine Berlin is currently the only German University Hospital with an available capacitive radiofrequency electromagnetic field treatment device. While there is retrospective data available regarding the assumed effectiveness and low toxicity profile of radiofrequency electromagnetic field treatment for various solid tumors including liver cancer, there is no prospective data available on the combined effect of first-line palliative double immune checkpoint inhibition and radiofrequency electromagnetic field treatment for patients with advanced hepatocellular carcinoma. The investigators aim to conduct a feasibility trial and plan to compare the results with data of a prospective trial with a comparable patient population who received double immune checkpoint inhibition alone.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Treatment with combined Anti-PD-L1 and Anti-CTLA-4 antibodies
  • Written informed consent prior to any study procedure
  • 18 years or older
  • Histologically confirmed HCC
  • HCC not amenable to curative (including resection or ablation) or locoregional (including TACE) therapies
  • No prior systemic therapy for HCC
  • Compensated liver function, as defined by a Child-Pugh score ≤ B7
  • Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2
  • Measurable disease by Response Criteria in Solid Tumors (mRECIST and RECIST v1.1) criteria
  • Body weight of > 30 kg
  • Women of childbearing potential with negative pregnancy test and agreement for adequate birth control if conception is possible
  • If present HBV and HCV managed according to the local institutional practice

Exclusion criteria

  • Arterioembolic event including a stroke or myocardial infarction within 3 months prior to randomization Severe / unstable angina, or symptomatic congestive heart failure as defined by NYHA III/IV
  • Cardiac pacemakers / ICD
  • Large metal implants in the treatment area
  • Current evidence of coagulopathy or bleeding diathesis
  • Known fibrolamellar HCC, sarcomatoid HCC, or mixed cholangiocarcinoma and HCC
  • Decompensated liver function as defined by Child Pugh ≥ B8
  • Patients on a liver transplantation list
  • Patients with autoimmune disorders or history of organ transplantation who require immunosuppressive therapy
  • Uncontrolled autoimmune or inflammatory disorders
  • Patient not able for supine positioning (e.g. due to pain)
  • Significantly altered mental status
  • Pregnancy and breastfeeding

Treatment and study plan

Radiofrequency electromagnetic field treatment

Device

Radiofrequency electromagnetic field treatment using a carrier frequency of 13.56 MHz

Primary outcomes

  1. Objective response rate (ORR)

    Time frame: Every 10-12 weeks until progression or a maximum follow-up of 3 years

    Objective response rate

Secondary outcomes

  1. Acute and late toxicity

    Time frame: During 4 years of trial conduction

    CTCAE version 5

  2. Quality of life (QoL)

    Time frame: During 4 years of trial conduction

    European Organisation for Research and Treatment of Cancer (EORTC) QLQ-C30

  3. Quality of life (QoL)

    Time frame: During 4 years of trial conduction

    European Organisation for Research and Treatment of Cancer (EORTC) QLQ-HCC18

  4. Progression-free survival (PFS)

    Time frame: During 4 years of trial conduction

    Progression-free survival

  5. Overall survival (OS)

    Time frame: During 4 years of trial conduction

    Overall survival

  6. Time to progression (TTP)

    Time frame: During 4 years of trial conduction

    Time to progression

  7. Duration of response (DOR)

    Time frame: During 4 years of trial conduction

    Duration of response

Study contacts

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

Pirus Ghadjar, Prof. Dr.

CONTACT

[email protected]

+49 30 450 527318

Sponsors and collaborators

Lead sponsor

Charite University, Berlin, Germany

Other

Registry information

Important dates

Study start
2025
Primary completion
2026
Study completion
2029
First posted
Feb 12, 2025
Registry last updated
Feb 12, 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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