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ctDNA Mutations and Methylation Status for Early Detection of Lung Cancer in Patients With Suspicious Lung Nodules

4 de junho de 2026 atualizado por: Dr. David Chi-leung Lam, The University of Hong Kong

Circulating Tumor DNA Mutations and Methylation Status as Biomarkers for Early Detection of Lung Cancer in Patients With Suspicious Lung Nodules

Lung Cancer is common in Asia and is different from lung cancer from Western countries in terms of lung cancer epidemiology and management. Lung cancer can be detected early but most early-stage lung cancer appear as lung nodules with suspicious features on imaging. Workup and surveillance for subjects with suspicious lung nodule is a clinical problem. There is no consensus and clinical practice usually varies with local epidemiology of lung diseases namely the local clinical characteristics especially with lung cancer and pulmonary tuberculosis. The clinical challenge is to address whether pulmonary nodules identified on CT screening carry short- and long-term risk for lung cancer. The main objective of this study is to test the improvement of efficiency of diagnostic evaluation with clinical parameters and ctDNA mutation/methylation profiling for artificial intelligence modeling of for early detection of lung cancer in subjects with suspicious lung nodules. The hypothesis is that ctDNA mutation and methylation will enhance early detection of lung cancer in patients with suspicious lung nodules. This is a longitudinal cohort study. A total of 200 subjects (100 from Hong Kong and 100 from Vietnam) with suspicious lung nodules on CT Thorax will be recruited. Blood samples will be collected at recruitment and subsequent 6 months follow up. ctDNA mutations and methylation with SPOTMAS Lung assays would be performed at baseline and at 6 months follow-up. The CT scan where the suspicious lung nodules were identified, will be used as baseline scan for recruitment. Recruited subjects will be arranged with a non-contrast LDCT scans at 6 months follow-up. The primary outcome measure of the study is the detection of ctDNA mutation and methylation in correlation with diagnosis of lung cancer or persistence of suspicious lung nodules. The secondary outcome measures of the study are the Sensitivity and specificity of clinical biomarkers in correctly identifying malignant lung nodule, i.e., lung cancer.

Visão geral do estudo

Descrição detalhada

In Asia, the incidence and mortality of lung cancer are both high . The clinical demographics of lung cancer patients in Asia are different when compared with western countries. Both in Hong Kong and in Vietnam, there is a prominence of female non-smokers with lung cancer in Hong Kong, with a male: female ratio of 1.5:1. The biology of lung cancers arising from non-smokers are believed to be different from lung cancers from smokers. This is well reflected in the heterogeneity of lung cancer cell types and also their respective mutation profiles. For instance, there are more female non-smokers with lung cancer with the cell types of being adenocarcinomas, with about half in proportion of them carrying EGFR mutations; whereas in male smokers with lung cancer, there are usually additional possibility of have squamous cell carcinomas, and the chance of the tumors carrying EGFR mutations is lower compared with non-smokers. Thus, different clinical biomarkers should be used for early detection of lung cancer in smokers and non-smokers. There is an urgent need to develop strategy for early detection of lung cancer in non-smokers who have no obvious risk factors like smokers. Blood-based biomarkers has the potential utility for identifying subjects with lung nodules showing high risk features for these lung nodules being malignant or becoming malignant. with whom additional workup for early diagnosis of lung cancer is indicated. What are lung nodules with suspicious features of malignancy? Lung nodules are primarily defined by size of 3 cm or less. They may come in variable numbers or in different lung areas. The radiological appearance could be completely solid nodule (CSN), heterogeneous part-solid/part-ground glass nodules (hGGN) or pure ground glass nodules (pGGN). hGGN and pGGN have been shown to be more likely to be malignant compared to CSN. The presence of calcification, or simply radiological reporting to be granuloma, or fat density inside the nodule is known to indicate benign nature. Lung nodules with irregular or spiculated border are likely malignant whereas smooth border and roundish appearance usually indicates benign lesion. Thus, there is always an element of likelihood or probability of malignancy based on radiological appearance, but it is not possible to tell with full confidence, from imaging features, that a lung nodule is malignant or not. With the often relatively small size and deep-seated location of lung nodules shown only on CT scan, invasive investigations for a lung nodule with tissue biopsy to confirm malignancy are associated with high morbidity. Non-invasive diagnostic biomarkers have become a unique chance of improvement of risk management for subjects at risk. The challenges related to sorting out a large majority of benign nodules from malignant ones and among those a majority of aggressive from indolent cancers. The key questions in determining individual probabilities of diseases, given their history, findings on CT, and biomarkers of risk, remain most challenging. Appropriate risk assessment in reducing the false positives associated with current low-dose computed tomography practices and identification of individuals who need therapy and at what time during tumor surveillance could reduce costs and morbidities associated with unnecessary interventions. Different blood-based biomarkers have been used alone or in combination in clinical practice. The most well-known one is Carcinoembryonic antigen (CEA). However, it is sensitive but not specific enough (raised level not limited to lung cancer but equally prevalent in colorectal tumor, and also inflammatory conditions). Newer biomarkers are urgently needed to enhance diagnosis of indeterminate or suspicious lung nodule. Recently, the development of a multimodal assay called SPOTMAS Lung assay that simultaneously profile methylomics, fragmentomics, DNA copy number, and end motifs in a single workflow of targeted and shallow genome-wide sequencing of cell-free DNA with the aim of early detection of lung cancer. This assay has shown good diagnostic performance of overall sensitivity of 94% for detection of lung cancer. Previous studies have shown that a quarter of patients with incidental pulmonary nodules experienced clinically significant distress that may relate to the poor knowledge about cancer risk and evaluation. Healthcare professionals have important roles to alleviate patients' distress through a good understanding of patients' level of understanding and distress related to lung nodules and social support systems. At the same time, it is important for physicians to know the applicability of available newer biomarker panels in different clinical situations to guide their respective clinical decisions.

The aim of this project is to use the assay of circulating tumor DNA mutations and methylomics to detect early lung cancer among subjects with suspicious lung nodules on lung imaging. The Key questions in determining individual probabilities of lung cancer, given their clinical history, findings on CT scan, and ctDNA mutation and methylation status for risk of early lung cancer, will be addressed. Reducing the false positives associated with current low-dose computed tomography practices and the identification of individuals who need therapy and at what time during tumor surveillance could reduce costs and morbidities associated with unnecessary interventions. Data will be collected and analyzed according to the list of primary and secondary outcomes.

The primary outcome measure of the study is - the detection of ctDNA mutation and methylation in correlation with diagnosis of lung cancer or persistence of suspicious lung nodules. The secondary outcome measures of the study are - the Sensitivity and specificity of clinical biomarkers in correctly identifying malignant lung nodule, i.e., lung cancer. The area under the summary receiver operating characteristic curve (AUC) and diagnostic odds ratio (DOR) with the ctDNA assay. Improvement of positive diagnostic likelihood ratio (DLR+) and negative diagnostic likelihood ratio (DLR-) of using the in diagnosing lung cancer. Cost-effectiveness in adding a clinical biomarker panel in enhancing risk stratification of lung nodules and hence diagnosis of lung cancer, defined as the incremental cost per additional lung cancer diagnosed.

The result from this project will provide means to early detection of lung cancer by ctDNA and methylomics assay. The Key questions in determining individual probabilities of lung cancer, given their clinical history, findings on CT, and ctDNA mutation and methylation status for risk of early lung cancer, will be addressed. Reducing the false positives associated with current low-dose computed tomography practices and the identification of individuals who need therapy and at what time during tumor surveillance could reduce costs and morbidities associated with unnecessary interventions. The impact of psychological stress associated with the diagnosis and surveillance of lung nodules could also be evaluated.

The information gained from this project will provide evidence-based practice guidance for diagnostic evaluation for lung nodules or lung cancer.

Tipo de estudo

Observacional

Inscrição (Estimado)

200

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Locais de estudo

      • Hong Kong, Hong Kong
        • University of Hong Kong Queen Mary Hospital
        • Contato:
          • David CL Lam, BSc,MBBS,PhD,FCCP,FACP,FRCP(E)
          • Número de telefone: 85222555814
          • E-mail: dcllam@hku.hk
        • Investigador principal:
          • David CL Lam, BSc,MBBS,PhD,FCCP,FACP,FRCP(E)
        • Subinvestigador:
          • Lynn YW Shong

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Não

Método de amostragem

Amostra Não Probabilística

População do estudo

People with suspicious lung nodules on CT Thorax

Descrição

Inclusion Criteria:

  1. Age 45 - 80 years;
  2. Suspicious lung nodules (> 0.5 - 30mm in longest diameter, non-calcified) found within the past six months, or if PET scan has been done before, the specific uptake value (SUV) should be more than 1

Exclusion Criteria:

  1. Age < 45 or > 80;
  2. Lung nodules of < 0.5 cm in longest diameter, or with calcification seen in imaging;
  3. Known lung cancer or lung metastasis before, or history of extra-pulmonary cancer;
  4. Active tuberculosis;
  5. Clinical unstable conditions including untreated ischemic heart disease or arrhythmia, uncontrolled airway disease;
  6. Unwillingness to undergo invasive investigation like bronchoscopy;
  7. Unable to provide informed written consent.

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
ctDNA mutation and methylation may contribute to the early identification of lung cancer in patients with suspicious lung nodules.
Prazo: 2 year study follow up and surveillance
The presence of ctDNA mutation and methylation features in relation to the diagnosis or persistence of suspicious lung nodules
2 year study follow up and surveillance

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Improving the accuracy of LDCT practices and supporting the identification of individuals who may benefit from further intervention at appropriate times Tumor surveillance could potentially impact costs and morbidities related to unnecessary intervention
Prazo: 2 year study follow up and surveillance

The performance characteristics of clinical biomarkers, including sensitivity and specificity, in differentiating malignant from non-malignant lung nodules, i.e. lung cancer. The area under the summary receiver operating characteristic curve (AUC) and diagnostic odds ratio (DOR) with the ctDNA assay.

Potential improvement in positive diagnostic likelihood ratio (DLR+) and negative diagnostic likelihood ratio (DLR-) of using the in diagnosing lung cancer.

An assessment of the cost-effectiveness of incorporating a clinical biomarker panel to enhance risk stratification of lung nodules and support diagnosis of lung cancer, expressed as the incremental cost per additional lung cancer diagnosed.

2 year study follow up and surveillance

Colaboradores e Investigadores

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Publicações e links úteis

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Publicações Gerais

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Estimado)

1 de junho de 2026

Conclusão Primária (Estimado)

1 de junho de 2028

Conclusão do estudo (Estimado)

1 de dezembro de 2028

Datas de inscrição no estudo

Enviado pela primeira vez

22 de maio de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

22 de maio de 2026

Primeira postagem (Real)

29 de maio de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

8 de junho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

4 de junho de 2026

Última verificação

1 de junho de 2026

Mais Informações

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Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

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