Abstract 187P
Background
Determining the radiosensitivity of an individual patient is pivotal in formulating an effective treatment strategy. However, the challenge has been the lack of reliable and clinically relevant predictive models for assessing radiosensitivity. In this study, we introduce a novel cancer organoid-based model called OncoSensi (Organoid Growth-based Oncological Sensitivity Test), which aims to predict an individual's response to radiotherapy and evaluate the risk of recurrence in patients with pharyngeal and esophageal cancer.
Methods
Biopsy tissues from 18 esophageal cancer patients and 14 pharyngeal cancer patients were dissociated into single cells and cultured on pillar plates with extracellular matrix (ECM) to establish cancer organoids array for high throughput radiation screening. These organoids were subsequently exposed to radiation doses of 2, 4, and 8 Gy. Post-irradiation, viable organoids were stained with calcein AM to assess survival. The area under the curve (AUC) and growth rate were calculated from viability data to determine the radiation sensitivity of each patient's organoids. Additionally, the patient's cancer stage score was integrated with these two parameters to generate the OncoSensi model and radiosensitivity prediction index.
Results
When individual parameters, such as the patient's AUC (conventional method), were employed, the radiation sensitivity prediction model showed specificity and sensitivity ranging from 50% to 70%. However, the organoid growth-based Oncological Sensitivity Test (OncoSensi) notably improved specificity to over 80% and sensitivity to over 80% in patients with pharyngeal and esophageal cancer. Additionally, OncoSensi identified a radiation-resistant group with a recurrence rate of over 50% within one year, distinguishing it significantly from the radiosensitive group in both pharyngeal and esophageal cancer patients.
Conclusions
Hence, the proposed OncoSensi proves valuable in predicting radiation response and recurrence among patients before undergoing radiation therapy for pharyngeal and esophageal cancers. It holds promise for application in precision medical platforms.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
D.W. Lee.
Funding
Medical & Bio Decision.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
142P - Exploring tumor mutational burden and frameshift mutations as predictors of immune checkpoint inhibitor efficacy
Presenter: Mai Hoshino
Session: Poster session 08
143P - Efficacy of immunotherapy in gastro-intestinal (GI) tumors with mismatch repair deficient (MMRd) unusual phenotype
Presenter: Emily Alouani
Session: Poster session 08
144P - Analysis of a novel predictive marker of immune checkpoint response in head and neck cancer, calculated from histopathological slides through inferred transcriptomics
Presenter: Johnathan Arnon
Session: Poster session 08
145P - Predicting the efficacy of immunotherapy in non-small cell lung cancer using machine learning based on simple clinical characteristics and biochemical indexes
Presenter: Lei Cheng
Session: Poster session 08
146P - Biomarkers and intrinsic/acquired resistance mechanisms for atezolizumab plus chemoradiotherapy in MSS locally advanced rectal cancer: An exploratory analysis of a single center, phase II study
Presenter: Wentao Tang
Session: Poster session 08
147P - Comparison of immune-checkpoint inhibitor therapy predictive marker tests microsatellite instability (MSI) and mismatch-repair deficiency (dMMR)
Presenter: Maja Nádorvári
Session: Poster session 08
148P - Clinical significance of CD4+ T cell subsets in peripheral blood for anti-PD-1/PD-L1 therapy
Presenter: Yoshimichi Haruna
Session: Poster session 08
149P - Evaluation of HLA genotype as predictive biomarker for immunological and clinical responses upon vaccination with PolyPEPI1018 cancer vaccine against colorectal cancer
Presenter: Joleen Hubbard
Session: Poster session 08
150P - Phase I/IIa trial of CD200R1 inhibitor 23ME-00610: Exploratory analyses of tissue-based and genetic biomarkers
Presenter: Albiruni Ryan Abdul Razak
Session: Poster session 08
151P - Enhanced pharmacodynamic effects upon combination of cibisatamab and FAP-4-1BBL in 3L+ mMSS CRC patients
Presenter: Ignacio Melero
Session: Poster session 08