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NCT Number: NCT05375591

AI & Radiomics for Stratification of Lung Nodules After Radically Treated Cancer

This study will assess the utility of radiomics and artificial intelligence approaches to new lung nodules in patients who have undergone radical treatment for a previous cancer.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Royal Brompton Hospital, London, United Kingdom

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About this study

Improvements in cancer detection and diagnosis have led to increasing numbers of patients being diagnosed with early stage cancer and potentially receiving curative therapy with improved survival outcomes. Recent retrospective studies in cancer survivors have demonstrated such patients possess an increased risk of further cancer in their lifetime compared to the general population, in part potentially due to shared lifestyle risk factors (e.g. smoking), genetic cancer pre-disposition or downstream oncogenic side effects of anti-cancer therapies (eg. radiotherapy). Lung cancer remains the leading cause of cancer related deaths worldwide and the lungs also represent a common site for metastatic disease in patients with non-pulmonary malignancy. Furthermore, lung cancer is one of the most common second primary malignancy in patients with a prior history of treated cancer. Therefore, discerning the significance of a pulmonary nodule in the context of a previous cancer remains a clinical challenge given it may possess the potential to represent benign disease, metastatic relapse or new primary malignancy.

This study will assess the utility of radiomics and artificial intelligence approaches to new lung nodules in patients who have undergone radical treatment for a previous cancer. This will entail use of machine learning (ML) approaches and later, exploration of deep-learning/convolutional neural network approaches to nodule interpretation for differentiation of benign, metastatic and new primary lung cancer nodules/lesions. Development of a ML classifier or deep learning based tool may help guide which patients would benefit from earlier investigations including additional imaging, biopsy sampling and lead to earlier cancer diagnosis, leading to better patient outcomes in this unique cohort. This is a retrospective study analysing data already collected routinely as part of patient care. All data will be anonymised prior to any analysis, no patient directed/related interventions will be employed and consent-waiver for study inclusion will be exercised.

Who can participate

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

Inclusion criteria

  • Confirmed history of previous radically or curative-intent treated solid organ cancer within 10 years of new index CT thoracic scan demonstrating a new pulmonary nodule and either of the following:
  • Biopsy confirming previous malignancy with MDT consensus and successful cancer resolution/remission following anti-cancer treatment on interval imaging or blood assay analysis
  • Where biopsy was not possible/confirmed for previous malignancy, MDT consensus outcome confirming cancer (+/- calculated Herder score >80% if applicable) and decision to treat as malignancy with subsequent resolution/remission following anti-cancer treatment on interval imaging or blood assay analysis
  • Radical treatment for previous cancer defined as either of the following:
  • Surgical resection
  • Radical radiotherapy or stereotactic beam radiotherapy
  • Radical chemotherapy
  • Radical chemo-radiotherapy
  • Multi-modality treatment with any of the above
  • New pulmonary nodule ground truth known
  • Scan data showing 2-year stability (based on diameter or volumetry) or resolution in cases of benign disease
  • Scan data showing progressive nodule enlargement or increase in nodule number on interval imaging with MDT consensus (+/- PET with Herder score >80% if applicable) determining metastatic disease or new primary malignancy
  • Biopsy sampling confirming benign disease or malignancy and in cases of malignancy, metastasis or new primary lung cancer
  • CT scan slice thickness ≤ 2.5mm
  • Nodule size ≥ 5mm

Exclusion criteria

  • CT Imaging > 10 years old
  • Non-solid haematological malignancies including leukaemia
  • Cases of radically treated primary cancer disease with early oligometastatic recurrence treated radically

Treatment and study plan

Non-Interventional Study

Other

First nodule detection CT scans as per eligibility criteria will be used as input into in-house software to extract multiple radiomic features and used to develop a machine learning based classifier to differentiate nodule aetiology. Scans will also be used as input in to a deep learning/convolutional neural network models to perform automated imaging classification.

Primary outcomes

  1. Development of a CT-thorax based radiomics ML classifier model to predict cancer risk in new lung nodules after previous radically treated cancer.

    Time frame: 2 years

    The study aims to identify distinct clusters of radiomics variables to generate a radiomics predictive vector (RPV), which can be used to stratify benign vs malignant nodules in patients who have previously received radical treatment for a malignancy. The RPV will be used in multivariate analysis and compared to existing risk models used in clinical practice.

  2. Development of the CT-thorax based ML classifier model to predict whether a new malignant nodule represents metastatic lung disease (new cancer vs previous cancer recurrence) or a new primary lung malignancy.

    Time frame: 2 years

    The study aims to identify distinct clusters of radiomic variables to generate a radiomics predictive vector (RPV) which is able to differentiate metastatic lung nodules from new primary lung cancer in patients who have previously received radical treatment for a cancer. No current models exist in clinical practice which address this diagnostic challenge.

Secondary outcomes

  1. To evaluate performance the developed CT-thorax based ML classifier model in an independent external validation cohort.

    Time frame: 2 years

    The investigators aim to assess performance of the derived radiomics predictive vector (RPV) on an external independent post-cancer lung nodule dataset to evaluate generalisability and potential real-world performance.

Study contacts

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

Laura Boddy

CONTACT

[email protected]

020 7808 2603

Sejal Jain

CONTACT

[email protected]

020 7808 2603

Sponsors and collaborators

Lead sponsor

Royal Marsden NHS Foundation Trust

Other

Collaborators

  • Imperial College London
  • Institute of Cancer Research, United Kingdom
  • National Heart and Lung Institute
  • National Institute for Health Research, United Kingdom
  • Oxford University Hospitals NHS Trust
  • Royal Brompton & Harefield NHS Foundation Trust
  • Royal Marsden Partners Cancer Alliance

Registry information

Official study title

Artificial Intelligence & Radiomics for Stratification Of Lung Nodules After Radically Treated Cancer (AI-SONAR)

Acronym: AI-SONAR

Important dates

Study start
2021
Primary completion
2022
Study completion
2026
First posted
May 16, 2022
Registry last updated
May 24, 2022

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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