Abstract 172P
Background
Pancreatic cancer is a disease with poor prognosis. Stereotactic body radiation therapy (SBRT) is emerging hope to achieve better resectability and local control. Pancreatic cancer treatment results are currently poorly predicted by the best clinical prediction algorithms. Through quantitative imaging analysis, radiomics and dynamic imaging characteristics can offer data on clinical outcomes and build clinical models based on imaging phenotypes or radiomics signatures. The objective of this pilot study was to analyze the association of CT based radiomic features with overall survival (OS) in pancreatic cancer patients treated with SBRT.
Methods
Ten patients of borderline resectable and locally advanced pancreatic cancer were included. All patients received neoadjuvant chemotherapy followed by SBRT and further chemotherapy and then assessed for surgery. Using pyRadiomics, radiomic features of gross tumour volume were extracted using contrast enhanced planning CT images acquired during SBRT planning. All the statistical analysis was performed using R software. Survival rates were analyzed using Kaplan-Meier survival curves.
Results
Three of the 10 patients were resected. Median follow-up was 15 months (range,5-24 months), median OS was 25 months. A total of 851 radiomic features [shape, first order, gray-level co-occurrence matrix (GLCM); grey level size zone matrix (GLSZM), gray-level distance zone matrix (GLDZM), grey level run length matrix (GLRLM) and grey level zone length matrix (GLZLM), gray-level co-occurrence matrix (GLCM); the neighborhood gray-level different matrix (NGLDM)] were extracted. Based on the radiomics score, patients were stratified into low and high risk categories.
Conclusions
This pilot study highlights the potential of CT-based radiomic features in predicting survival in patients with pancreatic cancer treated with chemotherapy followed by SBRT. The identified radiomic features, along with clinical parameters, offer valuable prognostic information that can aid in treatment decision-making and patient counseling. However, a larger number of patients are required to validate the results.
Editorial acknowledgement
Clinical trial identification
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
41P - HLA genotypes modify the age-related penetrance of BRCA1 pathogenic variants in breast cancer patients
Presenter: Ekaterina Kuligina
Session: Cocktail & Poster Display session
Resources:
Abstract
42P - Investigating the influence of extrachromosomal DNA in the progression of non-small cell lung cancer through the TRACERx and PEACE studies
Presenter: Jeanette Kittel
Session: Cocktail & Poster Display session
Resources:
Abstract
43P - MDM2 alterations in primary brain tumors: A potential niche for targeted therapy
Presenter: Diego Gomez Puerto
Session: Cocktail & Poster Display session
Resources:
Abstract
44P - Exploring miR-205 and miR-296 as salivary biomarkers and potential therapeutic targets in oral cancer
Presenter: Thaís Moré Milan
Session: Cocktail & Poster Display session
Resources:
Abstract
45P - Integrative analysis of TCGA DNA methylation, RNA-sequencing, and variant dataset using machine learning in predicting endometrial cancer recurrence
Presenter: Jinhwa Hong
Session: Cocktail & Poster Display session
Resources:
Abstract
46P - The role of microRNA-1246 in early detection of breast cancer: Findings from a systematic review and meta-analysis
Presenter: Muhammed Elfaituri
Session: Cocktail & Poster Display session
Resources:
Abstract
47P - Differential expression of discriminative markers in matched invasion fronts and tumour buds in CRC
Presenter: Laura Grech
Session: Cocktail & Poster Display session
Resources:
Abstract
48P - Transcriptome profiling highlights distinct gene signatures in HER2 high (HER2 3+) and HER 2 low (Her2 1+/2+) breast cancers
Presenter: Tamanna Thakur
Session: Cocktail & Poster Display session
Resources:
Abstract
49P - MiR-155 promotes breast cancer progression by upregulating cancer stemness
Presenter: Jeonghee Han
Session: Cocktail & Poster Display session
Resources:
Abstract
50P - Clinical impact of actionable molecular variants disclosed in late-stage cancer patients by tumor whole-exome sequencing in a prospective single-institution study
Presenter: Christophe Mapendano
Session: Cocktail & Poster Display session
Resources:
Abstract