The Dragon PLC Trial (DRAGON-PLC)

Last updated: May 12, 2025
Sponsor: Maastricht University
Overall Status: Active - Recruiting

Phase

N/A

Condition

Digestive System Neoplasms

Liver Cancer

Abdominal Cancer

Treatment

Portal Vein Embolization

Hepatic Vein Embolization

Clinical Study ID

NCT06914648
NL87590.0681.24
  • Ages > 18
  • All Genders

Study Summary

The goal of the DRAGON PLC clinical trial is to determine whether portal vein embolization (PVE) combined with hepatic vein embolization (HVE) improves resectability and overall survival in patients with initially unresectable primary liver cancer compared to standard PVE alone. This trial specifically focuses on patients with hepatocellular carcinoma and cholangiocarcinoma.

The main questions this trial aims to answer are whether combined PVE and HVE increases the proportion of patients who become resectable within 3 weeks and improves 5-year overall survival compared to PVE alone by enhancing liver hypertrophy.

Participants will:

  • Undergo either standard PVE or combined PVE and HVE.

  • Have regular imaging to assess liver resectability.

  • Be monitored for survival outcomes up to 5 years after intervention.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • PLC diagnosis, specifically iCCC, pCCC, and HCC;

  • Requiring PVE due to an FLR volume is <30% in normally functioning livers, <40% inlivers with potentially impaired function e.g. resulting from prior systemic therapyinduction or bile duct colonization / transpapillary biliary drainage, or <50% inlivers with severely impaired function resulting from liver cirrhosis (max. ChildPugh A5) OR function on hepatobiliary scintigraphy (HEBIS) is < 2.7 %/min/m2;

  • Age ≥ 18 years;

  • Able to understand the trial and provide informed consent.

Exclusion

Exclusion Criteria:

  • Liver cirrhosis with a Child-Pugh score of B or C;

  • Presence of portal hypertension;

  • Presence of cholangitis;

  • Pregnant women;

  • Premenopausal females not able/willing to commit to contraception (specificallylong-acting reversible contraception or hormonal contraception);

  • Patients unresectable due to prohibitive comorbidities (decision made by localmultidisciplinary team);

  • Patients with hepatic malignancies other than iCCC, pCCC or HCC;

  • PVE/HVE anatomically not feasible;

  • Any patient with non-resectable or non-ablatable extrahepatic metastatic disease.

  • Unable to understand the study information, study instructions and give informedconsent

Study Design

Total Participants: 358
Treatment Group(s): 2
Primary Treatment: Portal Vein Embolization
Phase:
Study Start date:
April 01, 2025
Estimated Completion Date:
November 15, 2032

Study Description

Primary liver cancer (PLC) is the third most common cause of cancer death worldwide. Surgical resection is the mainstay for a curative approach as contemporary chemotherapy and immune-based therapies only lead to a median survival of 10-14 months. A complete surgical resection increases the median survival to 42 months (range 32-52 months). However, PLC is mainly diagnosed at an advanced stage and >70% of PLC patients are ineligible for an immediate surgical approach. There are different reasons that make a patient ineligible for surgery, one important reason is the risk of liver failure after the surgery due to a small remnant liver.

This study aims to improve the oncological, radiological and surgical strategy to allow more patients to undergo liver resection safely, to improve quality of life and to extend overall survival at acceptable costs.

Adequate function of the future liver remnant (FLR) is a prerequisite for surgical resectability. This is necessary in order to avoid liver failure after surgery, a major cause of morbidity (38%) and mortality (27%). To mitigate this risk, regenerative strategies based on preoperative calculation of the FLR volume and function are essential. Patients with technically resectable disease but predicted insufficient FLR volume or function are referred to as primarily unresectable or potentially resectable (PU/PR). These patients can undergo strategies that capitalize on the regenerative capacity of the liver which aim to preoperatively increase the FLR volume and function in order to allow surgery. Many of the patients that are primarily unresectable due to an insufficient FLR can become ultimately and safely resectable after the induction of adequate FLR-hypertrophy by the current standard, portal vein embolisation (PVE). However, 25% of patients do not show sufficient FLR growth after PVE and are unable to safely undergo resection. A new approach has been developed to improve this. Combined portal and hepatic vein embolisation (PVE/HVE) has great promise in terms of increasing FLR growth, resection rate (RR), safety and potentially, overall survival. Establishing PVE/HVE as the new standard could result in increased survival and a better quality of life (QoL) for patients.

Connect with a study center

  • Monash Medical Center

    Melbourne,
    Australia

    Site Not Available

  • Medical University of Vienna

    Vienna, 1090
    Austria

    Site Not Available

  • Social Center South

    Vienna, 1100
    Austria

    Site Not Available

  • Erasmus Hospital

    Brussels, Bruxelles 1070
    Belgium

    Site Not Available

  • UZ Antwerpen

    Antwerp, Edegem 2650
    Belgium

    Site Not Available

  • CHU-UCL Namur site Godinne (UCLouvain)

    Yvoir, Namen 5530
    Belgium

    Site Not Available

  • Cliniques Universitaires Saint Luc, UCLouvain

    Brussels, 1200
    Belgium

    Site Not Available

  • UZ Gent

    Gent, 9000
    Belgium

    Site Not Available

  • Jessa Hospital

    Hasselt, 3500
    Belgium

    Site Not Available

  • UZ Brussel

    Jette, 1090
    Belgium

    Site Not Available

  • AZ Groeninge Hospital Kortrijk

    Kortrijk, 8500
    Belgium

    Site Not Available

  • CHU Liège

    Liège, 4000
    Belgium

    Active - Recruiting

  • Foothills Medical Center

    Calgary, Alberta
    Canada

    Site Not Available

  • Vancouver General Hospital

    Vancouver, British Columbia
    Canada

    Site Not Available

  • Queen Elizabeth II Health Sciences Center

    Halifax, Nova Scotia
    Canada

    Site Not Available

  • Juravinski Hospital and Cancer Centre

    Hamilton, Ontario
    Canada

    Site Not Available

  • Kingston Health Sciences Centre

    Kingston, Ontario
    Canada

    Site Not Available

  • London Health Sciences Centre

    London, Ontario
    Canada

    Site Not Available

  • St. Joseph's Health Centre

    Toronto, Ontario
    Canada

    Site Not Available

  • Sunnybrook Hospital

    Toronto, Ontario
    Canada

    Site Not Available

  • University Health Network/TGH

    Toronto, Ontario
    Canada

    Site Not Available

  • Centre Hospitalier Universitaire de Sherbrooke

    Sherbrooke, Quebec
    Canada

    Site Not Available

  • Centre Hospitalier de l'Université de Montréal

    Montreal,
    Canada

    Site Not Available

  • McGill University Health Centre, Montreal

    Montreal,
    Canada

    Site Not Available

  • L'Hopital d'Ottawa

    Ottawa,
    Canada

    Site Not Available

  • Royal University Hospital

    Saskatoon,
    Canada

    Site Not Available

  • Universitätklinikum Dresden

    Dresden,
    Germany

    Site Not Available

  • Universitätklinikum Hannover

    Hannover,
    Germany

    Site Not Available

  • Universitätklinikum Köln

    Köln,
    Germany

    Site Not Available

  • Ospedale San Raffaele

    Milan,
    Italy

    Site Not Available

  • Maastricht Universitair Medisch Centrum+

    Maastricht, Limburg 6229HX
    Netherlands

    Site Not Available

  • Amsterdam UMC, location VUMC

    Amsterdam, Noord Holland
    Netherlands

    Site Not Available

  • Maxima Medisch Centrum

    Eindhoven,
    Netherlands

    Site Not Available

  • Universitair Medisch Centrum Groningen

    Groningen,
    Netherlands

    Site Not Available

  • Leiden Universitair Medisch Centrum

    Leiden,
    Netherlands

    Site Not Available

  • Universitair Medisch Centrum Utrecht

    Utrecht,
    Netherlands

    Site Not Available

  • University Hospital Oslo

    Oslo,
    Norway

    Site Not Available

  • University Hospital Linköping

    Linköping,
    Sweden

    Site Not Available

  • Karolinska University Hospital Stockholm

    Stockholm,
    Sweden

    Site Not Available

  • Cantonal Hospital Winterthur

    Winterthur, Zürich
    Switzerland

    Site Not Available

  • Claraspital Basel

    Basel,
    Switzerland

    Site Not Available

  • Universitätsspital Basel

    Basel,
    Switzerland

    Site Not Available

  • CHUV - Lausanne University Hospital

    Lausanne,
    Switzerland

    Site Not Available

  • Hirslanden Klinik St. Anna

    Luzern,
    Switzerland

    Site Not Available

  • Hirslanden Klinik

    Zürich,
    Switzerland

    Site Not Available

  • Belfast Health and Social Care Trust

    Belfast,
    United Kingdom

    Site Not Available

  • Queen Elizabeth Hospital

    Birmingham,
    United Kingdom

    Site Not Available

  • Aintree University Hospital

    Liverpool,
    United Kingdom

    Site Not Available

  • Kings college Hospital

    London,
    United Kingdom

    Site Not Available

  • Oxford University Hospitals NHS Foundation Trust

    Oxford,
    United Kingdom

    Site Not Available

  • University Hospital Southampton

    Southampton,
    United Kingdom

    Site Not Available

  • Yale School of Medicine Hospital

    New Haven, Connecticut 06510
    United States

    Site Not Available

  • Rush University Medical Center

    Chicago, Illinois 60612
    United States

    Site Not Available

  • Mayo Clinic

    Rochester, Minnesota 55905
    United States

    Site Not Available

  • Memorial Sloan Kettering Cancer Center

    New York, New York 10065
    United States

    Site Not Available

  • Cleveland Clinic

    Cleveland, Ohio 44195
    United States

    Site Not Available

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