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Non Small Cell Lung CancerNCT06163846

Image Mining and ctDNA to Improve Risk Stratification and Outcome Prediction in NSCLC Applying Artificial Intelligence.

An observational study of Non Small Cell Lung Cancer, run by IRCCS San Raffaele at 1 site in Italy.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Lung cancer is the leading cause of cancer-related death in Europe. Pathological staging is the gold standard, but it can be influenced by neo-adjuvant treatment and number of sampled lymph nodes; it is not feasible in advanced stages and in patients with high-risk comorbidities. Read more about this study

Who is it for?
Ages 18 to 70 years
Conditions the study is for
Non Small Cell Lung Cancer
What is being tested?
Assess the role of baseline image mining, ctDNA data and their combination in patient staging and risk stratification
How many people
415 participants
Where
1 siteItaly
Study dates
10 Jul 2020to Jun 2025
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 70 years
  • All sexes
  • Adult, Older adult

Study population: This clinical research protocol will be an observational, prospective, bicentric, single-arm study. Patients newly diagnosed with non-small cell lung cancer will be eligible. 415 patients will be enrolled (of which 170 at San Raffaele Hospital). At the time of enrollment all eligible patients will sign the informed consent.

Who may be able to join

  • Patients with new pathological diagnosis of lung cancer, available baseline imaging (CT and FDG-PET/CT), age > 18 years, and eligibility for surgery will be considered for inclusion.

Who cannot join

  • pregnant or breast- feeding women.

Trial locations and contacts

1 site in 1 country.

Alessandra Maielli contact

0226433639

maielli.alessandra@hsr.it

Italy1 site, 1 recruiting
  • Irccs San Raffaele

    Milan, 20132

    Arturo Chiti

    Recruiting

Other trials in Italy

About this study

Lung cancer is the leading cause of cancer-related death in Europe. Pathological staging is the gold standard, but it can be influenced by neo-adjuvant treatment and number of sampled lymph nodes; it is not feasible in advanced stages and in patients with high-risk comorbidities. Therefore, patients with tumors of the same stage can experience variations in the incidence of recurrence and survival since suboptimal staging leads to inappropriate treatment that result in poorer outcomes. It is still undetermined what are the tumor characteristics that can accurately assess tumor burden and predict patient outcome.Our central hypothesis is that image-derived and genetic characteristics are consistent with disease stage and patient outcome. Combining through artificial intelligence techniques data coming from imaging and circulating cell-free tumor DNA (ctDNA) can provide accurate staging and predict outcome. This hypothesis has been formulated based on preliminary data and on the evidence that image-derived biomarkers by means of image mining (radiomics and deep learning algorithms) are able to provide "phenotype" and prognostic information. On the other hand, the analysis of ctDNA isolated from the plasma of patients has been proposed as an alternative method to assess the disease in the different phases, in particular, at diagnosis and after surgery, for detection of residual disease.

Read the detailed description

Our central hypothesis is that peculiar image-derived and genetic characteristics are consistent with disease stage and patient outcome. Therefore, they are biomarkers of disease burden and relapse, which can be non- invasively assessed. The combination through artificial intelligence methods of data coming from medical imaging and circulating cell-free tumor DNA (ctDNA) can provide accurate staging and outcome prediction. This hypothesis has been formulated based on the evidence that medical images are able to provide meanable data reflecting tumor characteristics, capturing intrinsic tumor heterogeneity, non-invasively, using a whole- body and whole-lesion assessment. In fact, in recent years, advanced analysis of medical imaging using radiomics, machine learning or in combination - image mining, has been explored. Image- derived biomarkers, by means of texture feature extraction and convolutional neural network application, have been tested to provide "phenotype" information (malignant vs benign, and histotype identification, and T or N staging. Moreover, correlations between image-derived quantitative features with tissue gene-expression patterns have been shown, linking the imaging phenotypes to the genotype as also demonstrated in our preliminary data. Secondly, image mining approach has been proposed to provide prognostic information at baseline evaluation, as also shown in our previous work. Still, few prospective studies with robust methodological approach have been published. On the other hand, the analysis of circulating cell-free tumor DNA (ctDNA) isolated from the plasma of lung cancer patients has been proposed as an alternative method to assess the disease in the different phases. In particular, at diagnosis, the post-surgical detection of residual disease, the identification of mutations in the metastatic setting for treatment guidance and monitoring treatment response. Even if, ctDNA has been detected in patients with all stages of NSCLC with levels increasing with stage and tumor burden ctDNA information has not been explored yet for the purpose of staging. The possibility to detect a tumor in the early phase of its development or the recurrence has to face the issue of the low amount of cfDNA in patients with minimal disease burden. Moreover, the presence of a para-physiological ctDNA background particularly in aged people affects the specificity. In this respect, the investigators expect that the combination of different biomarkers will allow to solve this problem.Artificial Intelligence analytics are increasingly described in healthcare applications. In recent years, supervised, semi-supervised, and unsupervised machine learning methods have been applied to analyze genomic, proteomic, clinical data and radiographical characteristics. Deep learning methods offer opportunities for comprehensive analysis of multi-dimensional data for improved prognosis prediction. The rationale for the proposed project is that, once it is known which imaging features and ctDNA-derived information is linked to the tumor stage and post-operative risk of relapse, the developed algorithm will be an effective and innovative approach for both staging and follow-up of patients affected by lung cancer, with implications on decision-making in clinical practice.

Being tested
Assess the role of baseline image mining, ctDNA data and their combination in patient staging and risk stratification
Medical subject headings
Carcinoma, Non-Small-Cell Lung

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Assess the role of baseline image mining, ctDNA data and their combination in patient staging and risk stratificationDiagnostic test

    Assess the combination of baseline and follow-up image mining, together with ctDNA, in predicting disease relapse and progression.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Artificial intelligence and circulating cell-free tumor DNA (ctDNA) for the staging and predict outcome in patients with with non-small cell lung cancer.

    Evaluate the prognostic role of advanced image analysis, ctDNA and their combination.

    Measured: 5 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted11 Dec 2023
  2. Study start10 Jul 2020
  3. Primary completion10 Dec 2020
  4. Study completionJun 2025 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
415 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06163846
Sponsor's protocol ID
AIRC_IG_2019_23596
Status last verified
Dec 2023
First submitted
23 Nov 2023
Last updated
20 Dec 2023
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

An observational study of Non Small Cell Lung Cancer, run by IRCCS San Raffaele at 1 site in Italy.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 20 Dec 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Alessandra Maielli (0226433639, maielli.alessandra@hsr.it), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Artificial intelligence and circulating cell-free tumor DNA (ctDNA) for the staging and predict outcome in patients with with non-small cell lung cancer. (time frame: 5 years). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 Dec 2023.

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