Lung Cancer, Predictive Cancer Model, Preinvasive Adenocarcinoma
Conditions
Keywords
Radiomics, Early stage, Pulmonary nodule, Pericancerous tissue, Immunotherapy
Brief summary
The purpose of this study was to investigate whether the combined radiomic model based on radiomic features extracted from focus and perifocal area (5mm) can effectively improve prediction performance of distinguishing precancerous lesions from early-stage lung adenocarcinoma, which could assist clinical decision making for surgery indication. Besides, response and long term clinical benefit of immunotherapy of advanced NSCLC lung cancer patients could also be predicted by this strategy.
Detailed description
Early detection and diagnosis of pulmonary nodules is clinically significant regarding optimal treatment selection and avoidance of unnecessary surgical procedures. Deferential pathology results causes widely different prognosis after standard surgery among pulmonary precancerous lesion, atypical adenomatous hyperplasia (AAH) as well as adenocarcinoma in situ (AIS), and early stage invasive adenocarcinoma (IAC). The micro-invasion of pulmonary perifocal interstitium is difficult to identify from AIS unless pathology immunohistochemical study was implemented after operation,which may causes prolonged procedure time and inappropriate surgical decision-making. Key feature-derived variables screened from CT scans via statistics and machine learning algorithms, could form a radiomics signature for disease diagnosis, tumor staging, therapy response adn patient prognosis. The purpose of this study was to investigate whether the combined radiomic signature based on the focal and perifocal(5mm)radiomic features can effectively improve predictive performance of distinguishing precancerous lesions from early stage lung adenocarcinoma. Besides, immunotherapy response is various among patients and no more than 20% of patients could benefit from it. None reliable biomarker has been found yet expect Programmed death-ligand 1 (PD-L1) expression, the only approved biomarker for immunotherapy. However recent reports suggested that patients could benefit from immunotherapy regardless of PD-L1 positive or negative. On the contrast, radiomics has show it advantages of non-invasiveness, easy-acquired and no limitation of sampling. Therefore, we applied this strategy in prediction for the immunotherapy response of advanced NSCLC lung cancer patients receiving immune checkpoint inhibitors (ICIs), which would prevent some non-benefit patient from the adverse effect of ICIs.
Interventions
Different radiomic and machine learning strategies for radiomic features extraction, sorting features and model constriction
Sponsors
Study design
Eligibility
Inclusion criteria
* (a) that were pathologically confirmed as precancerous lesions or Stage I lung adenocarcinoma (≤3cm) * (b) standard Chest CT scans with or without contrast enhancement performed \<3 months before surgery; * (c) availability of clinical characteristics.
Exclusion criteria
* (a) preoperative therapy (neoadjuvant chemotherapy or radiotherapy) performed, * (b) suffering from other tumor disease before or at the same time. * (c) Contain other pathological components such as squamous cell lung carcinoma (SCC) or small cell lung carcinoma (SCLC) or * (d) poor image quality. Inclusion Criteria of immunotherapy cohort: * (a) that were diagnosed as advanced NSCLC * (b) Both standard Chest CT scans with contrast enhancement performed \<3 months before and after first dose of immunotherapy are available; * (c) availability of clinical characteristics.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Pathological subtype | 5 years | Pathological type of pulmonary nodules |
| Objective Response Rate (ORR) | 5 years | Rate of ORR in all subjects for the patients who receiving immunotherapy |
| Progression-free survival (PFS) | 5 years | From enrollment to progression or death (for any reason) in immunotherapy cohort |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Overall survival (OS) | 5 years | From enrollment to death (for any reason) in immunotherapy cohort |
| Clinical Benefit Rate (CBR) | 5 years | Rate of CBR greater than or equal to 24 weeks in all subjects |
Countries
China