Phase
Condition
Carcinoma
Treatment
Radiofrequency electromagnetic field treatment
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
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 foradequate birth control if conception is possible
If present HBV and HCV managed according to the local institutional practice
Exclusion
Exclusion criteria:
Arterioembolic event including a stroke or myocardial infarction within 3 monthsprior to randomization Severe / unstable angina, or symptomatic congestive heartfailure 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 requireimmunosuppressive therapy
Uncontrolled autoimmune or inflammatory disorders
Patient not able for supine positioning (e.g. due to pain)
Significantly altered mental status
Pregnancy and breastfeeding
Study Design
Study Description
Connect with a study center
Charité University Medicine Berlin
Berlin, 13353
GermanyActive - Recruiting
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