Abstract 990P
Background
Hepatic arterial infusion chemotherapy (HAIC) is known to be more effective than conventional systemic chemotherapy, showing great potential in treating unresectable hepatocellular carcinoma (HCC) patients. However, there is still unclear which group can benefit more from HAIC.
Methods
191 patients with unresectable HCC undergoing HAIC from Zhongshan Hospital between May 2019 and March 2022 were retrospectively recruited. Radiomics scores were calculated based on enhanced-T1-weighted, enhanced-T2-weighted, arterial phase and delayed phase images. Clinical factors related to OS and PFS were identified by Cox regression analysis. Three different CNNs of AlexNet, ResNet, and Inception architectures were constructed on 70% of the data set and tested on the remaining 30%. Radiomics scores and clinical factors were reflected to a model eventually. Mean squared error (MSE) and time-dependent receiver operating characteristic curve were calculated for the models.
Results
The OS model included radiomics score with No. of HAIC cycles, tumor thrombus, PIVKA-II, neutrophil-lymphocyte ratio (NLR), aspartate aminotransferase (AST), gamma-glutamyltranspeptidase (γ-GT) and C-reactive protein. And the PFS model included radiomics score with No. of HAIC cycles, tumor thrombus, NLR and γ-GT. The AlexNet-OS model, ResNet-OS model, and Inception-OS model achieved the best MSE of 1.0068, 0.9023 and 0.8506, respectively. The AlexNet-PFS model, ResNet- PFS model, and Inception- PFS model achieved the best MSE of 0.6658, 0.6819 and 1.1012, respectively.
Conclusions
The present models which integrated radiomics information and clinical factors helped predict OS and PFS of unresectable HCC patients undergoing HAIC treatment.
Clinical trial identification
Editorial acknowledgement
We are very grateful to Mrs. Hailin Mi for helping us to construct the deep learning model. Hailin Mi kindly provided statistical advice for this manuscript. (Hailin Mi; Department of Computer Science and Technology, Harbin Engineering University, China)
Legal entity responsible for the study
The authors.
Funding
The National Natural Science Foundation of China (No. 81972889, Dr Yin).
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
956P - Phase II study of adjuvant tislelizumab combined with interferon-α and active surveillance in hepatocellular carcinoma patients with microvascular invasion
Presenter: Yixiu Wang
Session: Poster session 18
957P - Interim report of Notable-HCC: A phase Ib study of neoadjuvant PD-1 with stereotactic body radiotherapy in patients with resectable hepatocellular carcinoma (HCC)
Presenter: Mingming Li
Session: Poster session 18
959P - Combination therapy of envafolimab and suvemcitug in patients with hepatocellular carcinoma (HCC): Results from a phase II clinical trial
Presenter: Lixia Ma
Session: Poster session 18
960P - Personalized circulating tumor DNA (ctDNA) monitoring for recurrence detection and treatment response assessment in hepatocellular carcinoma (HCC)
Presenter: Maen Abdelrahim
Session: Poster session 18
961P - Blood circulating Galectin-3 is a prognostic biomarker in hepatocellular carcinoma
Presenter: Shadi Chamseddine
Session: Poster session 18
962P - SBRT improves the efficacy of immuno-checkpoint inhibitors for hepatocellular carcinoma through the activation of IL-6/JAK1-STAT3/PD-L1 axis mediated by MBD3 degradation
Presenter: Weiwei Yan
Session: Poster session 18
963P - Discovery and validation of cfDNA methylation, AFP and ctDNA mutation for the early detection of hepatocellular carcinoma: A multicenter prospective study (ASCEND-Hep)
Presenter: Mingxin Pan
Session: Poster session 18
966P - Potential role of neuropilin-1 in the prognosis, development and risk of invasion in hepatocellular carcinoma patients
Presenter: Tania Payo-Serafín
Session: Poster session 18