Abstract 551P
Background
PD-1/PD-L1 blockades with chemoradiotherapy as neoadjuvant therapy may promote tumor regression in patients with microsatellite stable (MSS) rectal cancer. However, which patient can benefit from this new treatment remains largely unknown, especially through analysis of magnetic resonance imaging (MRI) images.
Methods
Two phase II, open-labeled, studies evaluated the efficacy of anti-PD-1/PD-L1 to neoadjuvant chemoradiotherapy in MSS rectal cancer. Patients with locally advanced middle and low rectal cancer were recruited. All patients received long-course radiotherapy followed by two or three cycles anti-PD-1/PD-L1 treatment and radical resection surgery. Rectal MRI images were collected from patients prior to the radiotherapy. From each patient's rectal MRI set, three images where the tumor was clearly visible were selected and labeled. A convolutional neural network, named PDNet, was developed to extract features from these selected images and predict whether a pathological complete regression (pCR) is achieved.
Results
61 patients were recruited with 100% R0 resection. Among them, 24 patients achieved pCR (39.3%). A dataset comprising 183 rectal MRI images was utilized, with 147 images employed in the training phase and 36 images in the testing phase. After training, the PDNet model demonstrated strong performance on the test dataset (internal validations): it achieved a classification accuracy of 86.11%, a positive predictive value of 93.33%, a negative predictive value of 80.95%, a sensitivity of 77.78%, and a specificity of 94.44%. The model also recorded a p-value of 0.0000498 and an Area Under the Curve (AUC) of 0.8580, with a 95% Confidence Interval (CI) [0.6982, 0.9805].
Conclusions
The study concludes that features extracted from MRI images are highly correlated with the likelihood of achieving pCR. Using the developed neural network model (PDNet), we can predict the probability of achieving pCR before the treatment of PD-1/PD-L1 blockades with chemoradiotherapy in MSS local advanced rectal cancer. External validation of the model is currently underway.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
Jianmin Xu.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
479P - The candidate novel markers PIV and PILE score to predict survival outcomes and therapeutic response in patients with primary central nervous system lymphoma
Presenter: Ling Duan
Session: Poster session 16
Resources:
Abstract
480P - Clinical utility of ctDNA detection by NGS for diagnosis of CNS lymphoma
Presenter: Ana Jiménez-Ubieto
Session: Poster session 16
481P - Integrating GWAS and transcriptomics prioritizes drug targets for meningioma
Presenter: Wan-Zhe Liao
Session: Poster session 16
482P - The prognostic impact of CDKN2A/B heterozygous deletions in meningioma: Insights of a multicenter analysis
Presenter: Franziska Ippen
Session: Poster session 16
483P - The use of steroids associated with PD1/PDL-1 blockage in patients with brain metastasis: A systematic review and meta-analysis
Presenter: Francisco Cezar Moraes
Session: Poster session 16
484P - EGFR amplification is the potential driver gene that accelerates brain metastases in NSCLC patients
Presenter: Hainan Yang
Session: Poster session 16
485P - A spatio-temporal evolution mathematical model of glioma growth: The influence of cellular and nutrient interactions on the tumor microenvironment
Presenter: Kalysta Borges
Session: Poster session 16
486P - Effects of a BBB-penetrating oligonucleotide drug, RBD8088, in mouse models of human glioblastoma
Presenter: Julia Grönros
Session: Poster session 16
487P - 3D-bioprinted co-cultures of glioblastoma and mesenchymal cells indicate a role for perivascular niche cells in shaping the chemotactic tumour microenvironment
Presenter: Radosław Zagożdżon
Session: Poster session 16
488P - ITGA2 promotes glioma cell stemness and progression by activating the AKT pathway
Presenter: Lihui Wang
Session: Poster session 16