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
20P - Effects of <italic>Apis dorsata</italic> honey on the expression of selected CYP450, pro-apoptotic, and anti-apoptotic genes during induced cytotoxicity in cyclophosphamide-treated human lung carcinoma (A549) cells
Presenter: Jose Kenneth Narag
Session: Cocktail & Poster Display session
Resources:
Abstract
21P - Hsa_circ_0009061 inhibits the progression of bladder cancer through the miR-889-3p/CPEB3 axis
Presenter: Minkang Wu
Session: Cocktail & Poster Display session
Resources:
Abstract
22P - Exploring exportin-1 as a therapeutic vulnerability in lung squamous cell carcinoma
Presenter: Vidushi Durani
Session: Cocktail & Poster Display session
Resources:
Abstract
23P - Identification of HPSE as potential novel therapeutic target for lung adenocarcinoma patients
Presenter: Samuel Doré
Session: Cocktail & Poster Display session
Resources:
Abstract
24P - High-throughput plasma proteomics profiling in early breast cancer
Presenter: Isabella Lombardo
Session: Cocktail & Poster Display session
Resources:
Abstract
25P - Immunohistochemical analysis of ROR1 and BMI-1 expression in luminal breast cancer
Presenter: Sergey Vtorushin
Session: Cocktail & Poster Display session
Resources:
Abstract
26P - Associations between cancer stem cells (CSC) markers and androgen (AR) and estrogen (ER) receptors expression in prostate cancer (PCa)
Presenter: Marina Puchinskaya
Session: Cocktail & Poster Display session
Resources:
Abstract
27P - Proteomic profiling reveals organ-specific differences in metastases and identifies potential biomarkers for recurrence risk in localized colon cancer
Presenter: Blanca García-Micó
Session: Cocktail & Poster Display session
Resources:
Abstract
28P - Collagen-activated signalling pathway is significantly hypermethylated in high-grade serous ovarian cancer (HGSOC) patients treated with platinum-containing neoadjuvant chemotherapy (NACT)
Presenter: Jose Alejandro Perez Fidalgo
Session: Cocktail & Poster Display session
Resources:
Abstract
29P - Quantitative tissue analysis reveal adenylate kinase 2 protein signatures: Therapeutic target for meningioma
Presenter: Rashmi Rana
Session: Cocktail & Poster Display session
Resources:
Abstract