NCT06908005Completed
RaFIST: A Radiomics-Based Tool for Intratumoral Fibrosis Stratification in Non-Small Cell Lung Cancer
Development and Prognostic Validation of RaFIST: A Radiomics-Based Tool for Intratumoral Fibrosis Stratification in Non-Small Cell Lung Cancer
Source: ClinicalTrials.gov · Last updated 8 Apr 2025
Brief summary (registry, in English)
Patients with suspected Lung cancer who underwent contrast-enhanced CT and pathological examinations at Center 1 between January 2011 and January 2020 and Center 2 between September 2017 and Januray 2020 were eligible for inclusion in this study.The Clinical data, preoperative clinical information, laboratory results, CT images and pathological sections were collected. The investigators also collected the disease-free survival and overall survival time. On the Deepwise multi-modal research platform, the images were semi-automatically segmented and PyRadiomics was used to extract the radiomic features. Fibrosis quantification was performed on picrosirius red (PSR)-stained tissue sections using color deconvolution and binarized collagen signal analysis in ImageJ software. The investigators developed RaFIST, a radiomics-based stratification tool, to noninvasively quantify intratumoral fibrosis in non-small cell lung cancer (NSCLC) using contrast-enhanced CT imaging. And it was further tested on the held-out external test cohort. Discrimination was assessed by using the C-index and area under the receiver operating characteristic curve (AUC).
- Status (registry)
- Completed
- Study type
- Observational
- Enrollment
- 508 (actual)
- First submitted
- 1 Apr 2025
- Start date
- 1 Apr 2024
- Primary completion date
- 1 Dec 2024
- Lead sponsor
- Jinling Hospital, China
- Diseases
- Lung cancer
- NCT number
- NCT06908005
What you commit to
- Study type: Observational
- Participants enrolled: 508
- From 1 Apr 2024 to the primary completion date, 1 Dec 2024
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Undergone anticancer therapy before CT
- Concurrent other malignant tumors
Other
- Unavailable pathological sections
- Missing CT images or hard-to-annotate CT images
- Loss to follow-up
Who the study is looking for
- Solid pulmonary nodule detected on CECT within 3 weeks pre-resection
- No history of previous treatment such as chemotherapy, or radiotherapy
Age in the registry: 18 years to - · Sex: All
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Jinling Hospital Coordinator of this site? Confirm its status | Nanjing | China | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.