Clinical trial · Observational
Intelligent Support for Radiological Reporting of Lung Neoplasms
Intelligent Support for Radiological Reporting of Lung Neoplasms - SPOILERS Study
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Lung cancer is one of the most common cancers and has one of the worst prognoses, mainly due to the difficulty of early diagnosis. In Italy, there are an estimated 41,000 new cases each year, and in 2021, the disease was responsible for approximately 34,000 deaths. The social impact is significant, as the disease is often diagnosed at an advanced stage, when the chances of survival are reduced: the 5-year survival rate is around 18% in advanced stages, while it can reach 90% if diagnosed at an early stage. Early-stage lung cancer mainly manifests itself in the form of pulmonary nodules, which can be detected by computed tomography (CT). However, the diagnosis of these nodules often requires invasive procedures, such as bronchoscopy, CT-guided needle biopsy, or surgical biopsies, which affect patients' quality of life and healthcare costs. For this reason, the ability to accurately distinguish between benign and malignant nodules is a central theme in clinical research. In recent years, artificial intelligence, particularly deep learning techniques, has shown considerable potential in supporting CT screening. Results show that AI can achieve performance superior to that of individual radiologists and comparable to that of a multidisciplinary team, using histological reports as a diagnostic reference. This confirms the value of AI as a tool to support clinical decision-making. Considering the multimodal nature of clinical data (images, text reports, diagnostic tests), there is growing interest in models capable of integrating multiple sources of information. In this context, the research project aims to develop a system capable of automatically recognizing pulmonary nodules and generating natural language text descriptions of the findings.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Pulmonary Nodules | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Collection of variables identified for the study | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- label
- Patients with pulmonary nodules
- description
- Patients who have pulmonary nodules on computed tomography (CT) evaluation and who undergo biopsy will be enrolled.
- interventionNames
- Other: Collection of variables identified for the study
Primary outcomes (1)
- measure
- Development of a AI computer model
- timeFrame
- Through study completion, an average of 18 months
- description
- Development of a computer model that, through the application of artificial intelligence, is capable of recognizing and differentiating pulmonary nodules.
Secondary outcomes (1)
- measure
- Automatic generation of results by the AI model
- timeFrame
- Through study completion, an average of 18 months
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. Age ≥18 years 2. Evidence of pulmonary nodule documented radiologically by chest CT scan 3. Presence of CT scan report 4. Presence of histological report (pulmonary nodule biopsy) 5. Presence of written informed consent, signed Exclusion Criteria: 1. Previous cancer 2. Previous lung surgery 3. Previous radiation therapy and/or chemotherapy
References
Publications (0)
Data not yet available