Study on Adding Ipilimumab to Atezolizumab and Bevacizumab for Patients with Liver Cancer Receiving First-Line Treatment

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What is this study about?

This clinical trial is focused on studying a type of liver cancer known as hepatocellular carcinoma. The study is exploring the effects of adding a medication called Ipilimumab to a combination of two other medications, Atezolizumab and Bevacizumab. These medications are given as solutions through a vein, a method known as intravenous infusion. The purpose of the study is to evaluate whether this combination of treatments can improve outcomes for patients receiving their first systemic therapy for this type of cancer.

Participants in the study will be divided into two groups. One group will receive the combination of Atezolizumab and Bevacizumab, while the other group will receive all three medications, including Ipilimumab. The study will last for a period of up to 24 months, during which the effects of the treatments will be monitored. The main goal is to see if the addition of Ipilimumab can help improve the overall survival of patients compared to the two-drug combination. The study will also look at how well the cancer responds to the treatments and how long patients can live without the disease getting worse.

Throughout the study, participants will receive regular check-ups to monitor their health and the progress of their cancer. The study aims to provide valuable information on whether the addition of Ipilimumab offers a significant benefit in treating hepatocellular carcinoma. Participants will be closely observed for any side effects or changes in their quality of life during the treatment period. This research could potentially lead to improved treatment options for patients with this type of liver cancer.

1 joining the study

Upon joining the study, you will be randomly assigned to one of two treatment groups. This process is called randomization and ensures that each participant has an equal chance of receiving any of the treatments being tested.

2 treatment administration

You will receive medications through an intravenous infusion, which means the medicine will be given directly into your vein. The medications used in this study are ipilimumab, bevacizumab, and atezolizumab.

The specific combination and dosage of these medications will depend on the group you are assigned to. The treatment will be administered in cycles, with each cycle lasting a few weeks.

3 monitoring and assessments

Throughout the study, your health will be closely monitored. This includes regular check-ups, blood tests, and imaging tests to assess how the treatment is affecting your condition.

The main goal during the first 24 weeks (9 cycles) is to evaluate the response to the treatment, which could be a complete response, partial response, or no change.

4 continuation and follow-up

If the treatment is effective and you are tolerating it well, you may continue to receive it as part of the study. Your overall survival and quality of life will be assessed over time.

The study aims to compare the effectiveness of the treatment combinations in terms of overall survival and other health outcomes.

5 end of participation

Your participation in the study will conclude either when the study ends or if you choose to withdraw. You will be informed about the results of the study and any potential implications for your future treatment.

Who Can Join the Study?

  • Must be at least 18 years old.
  • Women who can have children must agree to use birth control during the trial and for at least 6 months after stopping the trial treatments. Men who have sex with women who can have children must also agree to use birth control during the trial and for at least 6 months after stopping the trial treatments.
  • Must be able to understand, sign, and date the informed consent form before being randomly assigned to a treatment group.
  • Must be part of a social security scheme.
  • Must have a confirmed diagnosis of hepatocellular carcinoma (HCC) through a biopsy done less than two years ago. If not confirmed, a liver biopsy is required.
  • Must have a WHO performance status of 0 or 1, which means being fully active or having some symptoms but still able to carry out light work.
  • HCC must not be treatable by surgery, heat treatment, liver transplant, or certain palliative treatments for intermediate stage HCC.
  • Must have advanced or intermediate HCC after failure or inability to use a specific treatment called CEL.
  • Must have normal levels of Troponin-T, a protein that helps diagnose heart problems.
  • Must not have visible fluid buildup in the abdomen (ascites) or a history of liver failure-related brain issues (encephalopathy).
  • Must have adequate liver function, with specific blood test results: AST and ALT levels no more than 5 times the upper normal limit, total bilirubin no more than 35 micromoles per liter, albumin at least 28 grams per liter, and a Child-Pugh A score if cirrhosis is present.
  • Must have adequate blood and kidney function, with specific test results: hemoglobin more than 8.5 grams per deciliter, platelets more than 60 billion per liter, neutrophils more than 1.5 billion per liter, and creatinine clearance at least 40 milliliters per minute.
  • Must have controlled heart disease for at least 6 months.
  • Must have at least one measurable tumor according to specific criteria (RECIST v1.1).
  • Must have had an esophageal endoscopy within the last 6 months. If varicose veins are found, they should be treated with beta-blockers unless there are reasons not to use them.

Who Cannot Join the Study?

  • Patients who have a different type of cancer other than hepatocellular carcinoma cannot participate.
  • Patients who have had another cancer treatment within the last 4 weeks are not eligible.
  • Patients with severe heart problems, such as heart failure or a recent heart attack, cannot join the study.
  • Patients with uncontrolled high blood pressure are not allowed to participate.
  • Patients with active infections, including HIV or hepatitis, are excluded.
  • Patients who are pregnant or breastfeeding cannot take part in the trial.
  • Patients with a history of severe allergic reactions to similar medications are not eligible.
  • Patients with significant liver disease, other than hepatocellular carcinoma, are excluded.
  • Patients who have had a major surgery within the last 4 weeks cannot participate.
  • Patients with a history of drug or alcohol abuse within the last 6 months are not eligible.
  • Patients who are unable to follow the study procedures or attend scheduled visits are excluded.

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Site Name City Country Status
University Hospital Of Clermont-Ferrand Clermont Ferrand France
Centre Hospitalier Universitaire De Lille Lille France
Centre Hospitalier Regional Et Universitaire De Brest Brest France
Institut Gustave Roussy Villejuif France
Centr Georges Francois Leclerc Dijon France
CHU Grenoble Alpes La Tronche France

Other Sites

Site Name City Country Status
Centre Hospitalier D Avignon Avignon France
Institut De Cancerologie Strasbourg Europe STRASBOURG, Alsace France
Centre Hospitalier Universitaire De Montpellier Montpellier France
Centre Hospitalier De La Cote Basque Bayonne France
Hopital Saint Joseph Marseille France
Centre Hospitalier Universitaire De Nice Nice France
Centre Hospitalier De Cholet Cholet France
Centre Hospitalier Universitaire Amiens Picardie Amiens France
Centre Hospitalier De Boulogne Sur Mer Boulogne sur Mer France
Hopital Saint Antoine Paris France
Centre Hospitalier De Perpignan Perpignan France
Centre Hospitalier Universitaire Rouen Rouen France
Hopitaux Universitaires Pitie Salpetriere Paris France
Clinique De L’infirmerie Protestante De Lyon Caluire Et Cuire France
Les Hopitaux Universitaires De Strasbourg STRASBOURG, Alsace France
Centre Hospitalier Universitaire De Toulouse Toulouse France
Centre Hospitalier Saint Joseph Saint Luc Lyon France
Centre Hospitalier Universitaire De Nantes Nantes France
Hopital Prive Des Cotes D’armor Plerin France
Grand Hopital De L Est Francilien Meaux France
Centre Hospitalier D Auxerre Auxerre France
Polyclinique Bordeaux Nord Aquitaine Bordeaux France
Hospital Foch Suresnes France
Centre Hospitalier Universitaire De Poitiers Poitiers France
IHFB Cognacq Jay Levallois-Perret France
Chorale Du Centre Hospitalier De Lens Lens France
Centre Hospitalier Jean Rougier Cahors France
Centre Hospitalier Bethune Beuvry Beuvry France
Centre Hospitalier Universitaire De Caen Normandie Caen France
L’Hopital Prive Du Confluent Nantes France
Centre Hospitalier De Pau Pau France
Centre De Lutte Contre Le Cancer Eugene Marquis Rennes France
Assistance Publique Hopitaux De Paris Creteil France
Groupe Hospitalier Rance Emeraude Saint-Malo France
Groupe Hospitalier Saint Vincent STRASBOURG, Alsace France
CHRU De Nancy Vandoeuvre Les Nancy France
Centre Hospitalier Pasteur Colmar France
Centre Hospitalier Saint Nazaire St Nazaire France
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Cbghab Haggvkowtld Vmuqyzb Valence France
Cna Cnazi Rdbdqwbrtwy Lyon France
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Iptxfslx dl Clcmohvriojs Hnvzyxhdpxk Uyrdrxjkloejp dd Spujg Etpqgvh (vmvfxbf Saint Priest En Jarez France
Icjmdvxb Pnhgztdkztwnxym Colpxs Ckzpnx Marseille France
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Want to learn more about this study or check if you can participate? Contact us.

Trial status

Country Status Recruitment Start
France France
Not recruiting
30.11.2022

Trial locations

Ipilimumab is a type of medication known as an immune checkpoint inhibitor. It works by helping your immune system recognize and attack cancer cells more effectively. In this trial, Ipilimumab is being tested to see if it can improve the treatment of liver cancer when added to other medications.

Atezolizumab is another immune checkpoint inhibitor. It helps your immune system fight cancer by blocking a protein that prevents your immune cells from attacking cancer cells. This medication is already used in treating some types of cancer, and the trial is exploring its effectiveness in liver cancer.

Bevacizumab is a medication that works by blocking the growth of blood vessels that supply nutrients to tumors. By cutting off the blood supply, it can help slow down or stop the growth of cancer. In this trial, Bevacizumab is being used in combination with other medications to see if it can improve outcomes for patients with liver cancer.

Hepatocellular carcinoma – Hepatocellular carcinoma is a type of liver cancer that originates in the hepatocytes, the main type of liver cell. It typically begins as a single tumor that grows larger over time, but it can also start as multiple small cancer nodules throughout the liver. As the disease progresses, it can invade nearby blood vessels and spread to other parts of the body, such as the lungs and bones. The progression of hepatocellular carcinoma is often associated with underlying liver conditions, such as cirrhosis or chronic hepatitis infection. Symptoms may include abdominal pain, weight loss, and jaundice, which can worsen as the disease advances. The growth rate and pattern of spread can vary significantly among individuals.

Trial ID:
2022-501217-31-00
Protocol code:
PRODIGE81-TRIPLET
Trial Phase:
Therapeutic use (Phase IV)

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