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Methylated Biomarkers of Smoking as a Selection Tool in Participants for Lung Cancer Screening (MET-SELS)

3 giugno 2026 aggiornato da: University Hospital, Antwerp

The MET-SELS study aims to revolutionize how we identify individuals for lung cancer screening by moving beyond the limitations of self-reported smoking history. Currently, eligibility for low-dose CT (LDCT) scans relies on "pack-years"-a metric often compromised by recall bias, under-reporting, and an inability to account for the biological nuances of smoke inhalation or environmental exposure. Consequently, current criteria miss nearly half of incidental lung cancers.

To bridge this gap, the study investigates DNA methylation as a stable, objective "biological footprint" of smoking. Unlike short-term biomarkers like nicotine or CO levels, specific epigenetic changes in genes such as AHRR and F2RL3 persist long after cessation and correlate accurately with cumulative tobacco exposure.

Led by Professor Dr. Annemiek Snoeckx and a multidisciplinary team at UZA and the Centre for Medical Genetics, the research will analyze saliva samples from two groups: roughly 900 participants from the ZORALCS screening trial and 150 volunteers. By comparing saliva-derived genomic signatures against both self-reported data and professional interviews, the team aims to validate a panel of methylation markers that can pinpoint high-risk individuals with far greater precision.

The ultimate vision for MET-SELS is to implement a population-based "saliva-first" triage system, similar to the FIT test used for colorectal cancer. In this model, high-risk candidates would provide a saliva sample at home; only those with a confirmed epigenetic risk profile would be invited for a LDCT scan, significantly increasing the yield of early-stage lung cancer detection while streamlining healthcare resources.

Panoramica dello studio

Descrizione dettagliata

The MET-SELS study represents a sophisticated paradigm shift in oncology and preventive medicine, aiming to solve one of the most persistent challenges in lung cancer screening (LCS): the accurate identification of the high-risk population. Currently, global screening protocols-which rely on low-dose CT (LDCT) scans-target individuals based on "categorical smoking criteria," typically defined by age and a history of at least 30 pack-years. However, as the MET-SELS researchers argue, these criteria are fundamentally flawed. They are largely arbitrary, susceptible to significant recall and volunteer bias, and fail to capture the biological reality of smoking behavior, such as inhalation depth, nicotine retention, or the compounding effects of second-hand smoke. Because current methods only capture approximately 50% of incidental lung cancers, there is a critical need for a "bias-proof" and biologically grounded selection tool.

To address this, the study, led by Principal Investigator Professor Dr. Annemiek Snoeckx and a multidisciplinary team including Professors Ken Op de Beeck, Guy Van Camp, and Jan van Meerbeeck, turns to the cutting-edge field of epigenetics. The central hypothesis is that tobacco smoke leaves a permanent and quantifiable "molecular scar" on the human genome through DNA methylation. While traditional biomarkers like carbon monoxide in exhaled breath or cotinine in serum only reflect short-term nicotine exposure-and can be easily masked by temporary abstinence or nicotine replacement therapy-DNA methylation patterns in specific genes are remarkably robust. Specifically, the study focuses on a panel of genes including AHRR, F2RL3, and ALPPL2. Research has shown that people who smoke or used to smoke exhibit significantly lower methylation levels at the AHRR site (cg05575921) compared to people who never smoked. Crucially, while some of these epigenetic markers begin to reverse upon quitting, others remain stable for more than 30 years after cessation, providing a reliable "biological ledger" of a person's lifetime tobacco exposure and their true risk profile.

The methodology of the MET-SELS study is designed for high statistical power and clinical relevance. It utilizes two distinct cohorts: Cohort 1 consists of 850-900 participants from the ZORALCS screening implementation study at UZA, and Cohort 2 includes 150 volunteers aged 50 and older, covering a spectrum of smoking histories. Participants provide a simple 2 ml saliva sample, which is far less invasive and more cost-effective for mass screening than blood-based liquid biopsies. These samples undergo rigorous genomic and methylomic analysis at the Centre for Medical Genetics, employing techniques such as whole-genome sequencing (WGS) and quantitative methylation-specific PCR (qMSP). These biological results are then cross-referenced against two types of behavioral data: self-reported questionnaires and intensive, structured interviews led by specialized healthcare providers. By using ROC analysis and linear regression, the study aims to validate how accurately these salivary biomarkers can predict smoking status, pack-years, and duration of abstinence compared to traditional reporting.

The long-term vision of MET-SELS is nothing short of a total transformation of public health policy. The researchers aim to validate a "saliva-first" triage model for lung cancer, analogous to the FIT (Fecal Immunochemical Test) used in colorectal cancer screening. In this envisioned future, a saliva collection kit would be mailed to the target-age population; only those whose epigenetic signature reveals a high-risk profile would be invited for a clinical LDCT scan. This approach would not only improve the yield of early-stage lung cancer detection but also significantly enhance the cost-effectiveness of screening programs by excluding low-risk individuals who are currently selected based on inaccurate self-reporting. By replacing subjective anecdotes with objective genomic data, the MET-SELS study paves the way for a more precise, equitable, and effective era of cancer prevention.

Tipo di studio

Interventistico

Iscrizione (Stimato)

1000

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Luoghi di studio

    • Antwerpen
      • Antwerp, Antwerpen, Belgio, 2650

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

Descrizione

Cohort 1: Volunteers

Inclusion Criteria:

  • Age: Must be > 50 years of age
  • Smoking History: Includes individuals with and without a smoking history

Cohort 2: ZORALCS-study participants

Inclusion Criteria:

  • Age: 55-74 years old
  • Smoking History: Includes individuals with a smoking history

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Selezione
  • Assegnazione: Non randomizzato
  • Modello interventistico: Assegnazione di gruppo singolo
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Cohort - volunteers
Reference group: people who smoked less than 10 years
Participants provide a simple 2 ml saliva sample, which is far less invasive and more cost-effective for mass screening than blood-based liquid biopsies. These samples undergo rigorous genomic and methylomic analysis at the Centre for Medical Genetics, employing techniques such as whole-genome sequencing (WGS) and quantitative methylation-specific PCR (qMSP). These biological results are then cross-referenced against two types of behavioral data: self-reported questionnaires and intensive, structured interviews led by specialized healthcare providers. By using ROC analysis and linear regression, the study aims to validate how accurately these salivary biomarkers can predict smoking status, pack-years, and duration of abstinence compared to traditional reporting.
Sperimentale: Cohort: Lung cancer screening participants
Participants of the ZORALCS-study
Participants provide a simple 2 ml saliva sample, which is far less invasive and more cost-effective for mass screening than blood-based liquid biopsies. These samples undergo rigorous genomic and methylomic analysis at the Centre for Medical Genetics, employing techniques such as whole-genome sequencing (WGS) and quantitative methylation-specific PCR (qMSP). These biological results are then cross-referenced against two types of behavioral data: self-reported questionnaires and intensive, structured interviews led by specialized healthcare providers. By using ROC analysis and linear regression, the study aims to validate how accurately these salivary biomarkers can predict smoking status, pack-years, and duration of abstinence compared to traditional reporting.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
DNA-methylation
Lasso di tempo: 3 years
DNA Methylation Status, measured as a continuous variable across a panel of specific genes (e.g., AHRR, F2RL3, ALPPL2).
3 years

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Comparative smoking accuracy
Lasso di tempo: 2 years
Self-reported vs. Interview-based Accuracy: Comparing how well the DNA markers correlate with the participant's own questionnaire answers versus the data gathered by a specialized healthcare professional
2 years

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Collaboratori

Investigatori

  • Investigatore principale: Annemiek Snoeckx, MD, PhD, University Of Antwerp / Antwerp University Hospital

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

4 ottobre 2025

Completamento primario (Stimato)

1 gennaio 2027

Completamento dello studio (Stimato)

1 gennaio 2028

Date di iscrizione allo studio

Primo inviato

4 maggio 2026

Primo inviato che soddisfa i criteri di controllo qualità

3 giugno 2026

Primo Inserito (Effettivo)

8 giugno 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

8 giugno 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

3 giugno 2026

Ultimo verificato

1 aprile 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • 4607 (Altro identificatore: Antwerp University Hospital)

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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