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NCT04705389Active, not recruiting

SerUM Markers in MERkel Cell Carcinoma Patients: a Longitudinal moniTorIng Study for optiMization of European Guidelines

Source: ClinicalTrials.gov · Last updated 12 Jun 2026

Brief summary (registry, in English)

Merkel cell carcinoma (MCC) is a rare aggressive skin carcinoma. Approximately 80% of MCC are related to the Merkel Cell Polyomavirus (MCPyV). Although rates of relapse are high, the follow-up strategy lacks consensus. Patients are usually assessed clinically every 3 to 6 months for the first 2-3 years, and every 6 to 12 months thereafter. In the European guidelines, patients with early stages are monitored with clinical examination and ultrasonography of lymph nodes, while whole-body imaging is optional in patients with stage III disease, on a yearly basis for 5 years. Such strategy may prevent the diagnosis of infra-clinical recurrences, whereas patients could still be treated with surgery or radiation therapy. Until 2017, patients with advanced disease were treated with chemotherapies, with no long-term benefit. Immunotherapies with PD-1/PD-L1 inhibitors currently allow durable responses in 50% of such patients. This major change in the management of MCC patients argues for a follow-up strategy that would allow early diagnosis of infra-clinical metastases, when tumoral burden is still low. Given that all patients cannot be monitored by systematic regular imaging, additional non-invasive tools are needed. Blood-based biomarkers as a surrogate of tumor burden are advantageous as they can be repeated over time, providing guidance on when imaging is necessary. The study aims to assess two blood biomarkers, MCPyV T-Ag antibodies and cell-free miR-375, in a prospective fashion from baseline diagnosis, in a cohort of 150 European MCC patients

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
35 (actual)
First submitted
8 Jan 2021
Start date
5 Dec 2022
Primary completion date
5 Dec 2025
Lead sponsor
University Hospital, Tours
NCT number
NCT04705389

What you commit to

  • Study type: Interventional
  • Participants enrolled: 35
  • From 5 Dec 2022 to the primary completion date, 5 Dec 2025
  • 10 sites in 10 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Patients following any measures of legal presentation
  • Pregnancy or breastfeeding

Who the study is looking for

  • Patients with a " de novo " diagnosis of MCC, confirmed on histological criteria (neuroendocrine morphology, CK20 staining and/or neuroendocrine and/or SATB2 staining, exclusion of differential diagnosis)
  • ≥ 18 years of age
  • Written informed consent obtained from the participant

Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (10)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Department of Dermatology, Medical University of Vienna
Coordinator of this site? Confirm its status
ViennaAustriaUnknown status
Translational Skin Cancer Research
Coordinator of this site? Confirm its status
EssenGermanyUnknown status
University Hospital of Helsinki, Finland
Coordinator of this site? Confirm its status
HelsinkiFinlandUnknown status
Dermatology Dept, Hospital University of Tours
Coordinator of this site? Confirm its status
ToursFranceUnknown status
Queen Elizabeth Hospital
Coordinator of this site? Confirm its status
BirminghamUnited KingdomUnknown status
National Tumour Institute "Fondazione G. Pascale" Unit of Melanoma - Cancer Immunotherapy and Innovative therapy
Coordinator of this site? Confirm its status
NaplesItalyUnknown status
Academic Hospital of Maastricht
Coordinator of this site? Confirm its status
MaastrichtNetherlandsUnknown status
Department of Dermatology, Carol Davila University of Medicine and Pharmacy
Coordinator of this site? Confirm its status
BucharestRomaniaUnknown status
Skin Cancer and Surgery Center, Sahlgrenska University Hospital
Coordinator of this site? Confirm its status
GothenburgSwedenUnknown status
Department of Dermatology, Başkent University Faculty of Medicine
Coordinator of this site? Confirm its status
AnkaraTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.