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NCT Number: NCT06546007

Rarecells Molecular Biomarkers for Early Detection of Lung Cancer

Early diagnosis of lung cancer is a public health priority. Additionally, early detection of recurrences after treatment is crucial for optimizing disease management.

This study seeks to demonstrate the accuracy of the Rarecells ISET® circulating tumor cells DNA (CTC-DNA), combined with circulating tumor DNA (ctDNA), for the early diagnosis of lung cancer.

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Key information

Age range

35 year–85 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Università Cattolica del Sacro Cuore Gemelli Hospital

Roma, Italy

Location status: Recruiting

Location contact

Filippo Lococo, MD

CONTACT

Filippo Lococo, MD

PRINCIPAL_INVESTIGATOR

About this study

Researching for tumor biomarkers in the blood, circulating tumor cells (CTCs), and circulating tumor DNA (ctDNA) can non-invasively detect signs of cancer without risk to the patient. These are ideal and risk-free methods for monitoring patients and early detection of lung cancer.

This study aims to assess the sensitivity of molecular analyses performed on circulating tumor DNA in the blood and on DNA from circulating tumor cells, isolated using the highly sensitive ISET® method. The purpose is to assess two circulating molecular biomarkers in the field of liquid biopsy in patients with lung cancer: Rarecells ISET® CTC-DNA and ctDNA.

Subjects eligible for inclusion in the study are individuals diagnosed with operable lung cancer who will undergo biopsy or surgical resection of the tumor. Upon enrolment in the trial, participants will undergo an assessment including low-dose CT scan, isolation of CTCs by the ISET® method, and separation of plasma for analysis of ctDNA.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male or female aged between 35 and 85 years
  • Patient diagnosed with resectable lung cancer (by imaging and/or pathological examination) not yet treated for this cancer.
  • Patient capable of giving free, informed, and express consent

The assessment of successful elected surgery implies, but is not limited to, the following:

  • Exclusion of detectable extra thoracic and distant metastases
  • Determination of the presence or absence of superior mediastinal lymph node metastases
  • Definition of the histologic or cell type, whenever possible
  • Evaluation of operative risk

Exclusion criteria

  • Patient diagnosed and/or treated previously for lung cancer or another cancer, regardless of duration
  • Patient treated with neoadjuvant treatment
  • Pregnant women
  • Patient presenting psychiatric or neurological disorders preventing them from understanding the research

Treatment and study plan

CTC-DNA

Diagnostic Test

ctDNA for the analysis of lung cancer mutations in patients with operable tumors.

Other names: ctDNA

Primary outcomes

  1. Comparative and complementary in operable patients diagnosed with cancer

    Time frame: 30 days post procedure

    Number of patients with lung cancer-related mutations by CTCDNA alone, by ctDNA alone and by the ctDNA -CTCDNA pair divided by the number of patients with cancer enrolled in the study

Secondary outcomes

  1. Comparative and complementary sensitivity of CTC-DNA and ctDNA per histological subtype

    Time frame: 30 days post procedure

    Number of patients with lung cancer-related mutations by CTCDNA alone, by ctDNA alone and by the ctDNA -CTCDNA pair per histologic subtype

Study contacts

Contact information is provided by the study sponsor or research team.

Monica Tocchi, MD, PhD

CONTACT

[email protected]

6469331025

Sponsors and collaborators

Lead sponsor

Rarecells Diagnostics SAS

Industry

Collaborators

  • Meditrial Europe Ltd.
  • Meditrial SrL

Registry information

Official study title

Clinical Study To Evaluate the Sensitivity of Circulating Iset® by Rarecells Molecular Biomarkers for Early Detection of Lung Cancer

Acronym: BioMolCTC

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Aug 9, 2024
Registry last updated
Jun 11, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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