Study of Retifanlimab Combined with Carboplatin, Cisplatin and Etoposide Before Surgery in Patients with Resectable Merkel Cell Carcinoma

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What is this study about?

This study focuses on patients with Merkel Cell Carcinoma that can be removed by surgery and has not spread to other organs. The treatment combines several medications: retifanlimab (also known as ZYNYZ), which is given together with chemotherapy drugs including carboplatin or cisplatin, and etoposide. All medications are given through an intravenous infusion into a vein.

The purpose of this study is to test how well a short course of combined chemotherapy and immunotherapy works when given before surgery in patients with Merkel Cell Carcinoma. The treatment involves one cycle of therapy followed by an operation to remove the tumor. During the treatment, patients will receive the medications through intravenous infusions at specified doses.

After the surgery is completed, doctors will examine the removed tumor tissue to determine if any cancer cells remain. The study will also look at how safe the treatment is and how it affects patients’ quality of life. Researchers will collect blood samples and tumor tissue to study how the treatment affects the cancer cells and the body’s immune system.

1 Initial treatment phase

You will receive a combination of medications through intravenous infusion. The treatment includes:

Retifanlimab (ZYNYZ 500 mg)

Platinum-based chemotherapy (either cisplatin or carboplatin)

Etoposide

This treatment consists of one cycle before surgery.

2 Surgery

After completing the medication cycle, you will undergo surgery to remove the tumor.

The surgical team will remove the tumor and examine nearby lymph nodes.

3 Medical evaluations

Throughout the study, you will undergo regular health assessments including:

– Blood tests to check blood cell counts, liver, and kidney function

– Physical examinations

– Vital signs monitoring

– Heart activity checks (ECG)

– Quality of life questionnaires

4 Follow-up period

After surgery, you will have regular follow-up visits to monitor your recovery and health status.

The study team will track your progress to assess whether the cancer returns.

The total duration of follow-up will continue until the end of 2026.

5 Sample collection

Throughout the study, samples will be collected to analyze your response to treatment:

– Tumor tissue samples before and after treatment

– Blood samples for analysis

These samples help evaluate how well the treatment is working.

Who Can Join the Study?

  • Must be at least 18 years old
  • Must sign an informed consent form
  • Must have a confirmed diagnosis of Merkel cell carcinoma that can be surgically removed
  • Must not have received any previous systemic treatment or radiation therapy before surgery
  • Must be able to perform daily activities independently or with minimal assistance (ECOG status 0-1)
  • Must be willing to attend scheduled appointments and follow the treatment plan
  • Must provide tumor tissue samples for analysis
  • Must have adequate blood test results showing:
    • Platelet count of at least 100,000 per microliter
    • White blood cell count of at least 1,500 per microliter
    • Hemoglobin level of at least 9.0 g/dL
  • Must have proper kidney function as shown by blood tests
  • Must have proper liver function as shown by blood tests
  • For women who can become pregnant:
    • Must have a negative pregnancy test
    • Must use effective birth control during the study and for 180 days after
  • For men:
    • Must use effective birth control during the study and for 6 months after
    • Must not donate sperm during this period

Who Cannot Join the Study?

  • Previous treatment with any anti-cancer therapy for Merkel cell carcinoma
  • Having cancer that has spread to other organs (metastases)
  • Tumor that cannot be removed by surgery
  • History of autoimmune diseases (conditions where the immune system attacks healthy cells)
  • Active or chronic infections including hepatitis B, hepatitis C, or HIV
  • Severe heart conditions in the past 6 months
  • Uncontrolled high blood pressure
  • Pregnant or breastfeeding women
  • Known allergies to the study medications
  • Mental conditions that could interfere with following study procedures
  • Major surgery within 4 weeks before starting the study
  • Participation in other clinical trials within 4 weeks before this study
  • Any condition that the doctor believes would make participation unsafe

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

No sites found in this category

Other Sites

Site Name City Country Status
Istituto Oncologico Veneto Padua Italy
Istituto Europeo Di Oncologia S.r.l. Milan Italy
IRCCS Istituto Nazionale Tumori Fondazione Pascale Naples Italy
Azienda Ospedaliero Universitaria Di Modena Modena Italy
Fondazione Luigi Maria Monti Rome Italy
Istituto Tumori Bari Giovanni Paolo II Bari Italy
Universita’ Degli Studi Di Perugia Perugia Italy
IRCCS Ospedale Policlinico San Martino Genoa Italy
Universita Degli Studi Di Brescia Brescia Italy
Fondazione I.R.C.C.S. Istituto Neurologico Besta Milan Italy
Azienda Ospedaliero Universitaria Pisana Pisa Italy
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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
Italy Italy
Not recruiting
01.12.2022

Trial locations

Retifanlimab is an immunotherapy medication that helps the immune system fight cancer cells. It belongs to a group of drugs called immune checkpoint inhibitors, which work by blocking certain proteins that prevent the immune system from attacking cancer cells.

Etoposide is a chemotherapy medication that works by stopping cancer cells from growing and dividing. It is commonly used in combination with other chemotherapy drugs to treat various types of cancer.

Platinum (such as cisplatin or carboplatin) is a type of chemotherapy medication that damages the DNA of cancer cells, preventing them from multiplying. It is often used in combination with other chemotherapy drugs to increase effectiveness in treating cancer.

Merkel Cell Carcinoma – A rare type of skin cancer that typically appears as a flesh-colored or bluish-red nodule on the skin’s surface. It usually develops on sun-exposed areas of the body, most commonly on the face, head, or neck. The cancer begins in Merkel cells, which are located at the base of the epidermis and are connected to nerve endings that sense touch. This cancer tends to grow quickly in the skin’s top layer and can spread to nearby lymph nodes. Merkel cell carcinoma often appears as a painless, firm bump that can be red, purple, or skin-colored. The condition primarily affects older adults and those with weakened immune systems.

Trial ID:
2024-516316-13-00
Protocol code:
MERCURY
Trial Phase:
Therapeutic exploratory (Phase II)

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