Abstract 191P
Background
Carcinotech's 3D bioprinted tumour models offer a transformative platform for advancing cancer drug screening and therapeutic testing by accurately replicating the complexity of the tumour microenvironment (TME). Unlike traditional 2D cultures, organoids, or animal models, these bioprints incorporate multiple cell types from patient-derived cancer tissues in a robust tissue matrix, providing a more biologically relevant model for preclinical studies, particularly in immuno-oncology and personalised medicine. Our recent research shows that these models effectively represent the presence of tumor-infiltrating lymphocytes (TILs), a crucial immune cell group targeted by advanced immunotherapies.
Methods
Patient ovarian tumour biopsies were sectioned, processed into FFPE blocks and TME characterised using immunofluorescence (IF) technique. Patient-derived cells were cultured as a heterogeneous population and 3D-bioprinted with custom bioink onto 96-well plate format. After 14 days in culture, characterisation of 3D-model TME composition was performed to compare it to the original tumour to assure high TME representation. Additionally, Carcino3D ovarian cancer models were treated with well-established immunotherapeutics Pembrolizumab and Rituximab, and activation of immune markers using IF as well as pro-inflammatory release of Granzyme B post-treatment tested.
Results
While the viability of the Carcino3D tumour model slightly declined after treatment, we observed stronger immune responses, including cytokine release, when treated with Pembrolizumab or Rituximab. Through advanced 3D imaging and AI-based analysis, we identified an increase in T-cell numbers post-treatment. Interestingly, early-stage T-cell activation decreased, while late-stage activation markers increased, confirming the models' accuracy in predicting therapeutic outcomes.
Conclusions
These findings highlight the potential of Carcinotech's 3D bioprinted models to significantly accelerate immunotherapy research and improve drug development pipelines. By offering a more dynamic and representative testing platform, these models promise to reshape the future of cancer drug discovery and personalised treatment approaches.
Legal entity responsible for the study
Carcinotech Ltd.
Funding
Carcinotech.
Disclosure
K. Pawlicka, M. McDonald, B. Kennedy, V. Metodieva, J. Adams: Financial Interests, Institutional, Full or part-time Employment: Carcinotech.
Resources from the same session
134P - Intracranial (IC) progression-free survival (PFS) with ivonescimab (Ivo) compared to placebo in the HARMONi-A trial of patients (Pts) with previously treated EGFR mutation-positive (EGFRm+) non-small cell lung cancer (NSCLC)
Presenter: Li Zhang
Session: Poster Display session
Resources:
Abstract
135P - Efficacy and safety of tislelizumab combined with bronchial arterial infusion (BAI) chemotherapy in potentially resectable stage IIIB non-small cell lung cancer(NSCLC): A prospective, single-arm phase II clinical study
Presenter: Xu Ma
Session: Poster Display session
Resources:
Abstract
136P - Tislelizumab (TIS) plus chemotherapy (chemo) with or without bevacizumab (beva) for patients with EGFR-mutated nonsquamous NSCLC (nsq-NSCLC) after progression on EGFR tyrosine kinase inhibitor (TKI) therapy: An updated analysis
Presenter: Baohui Han
Session: Poster Display session
Resources:
Abstract
137P - Hepatic arterial infusion chemotherapy combined with lenvatinib and tislelizumab for unresectable hepatocellular carcinoma: A single-arm, phase II study
Presenter: Jianbing Wu
Session: Poster Display session
Resources:
Abstract
138P - Interim results of neoadjuvant TACE plus lenvatinib and tislelizumab in resectable HCC at CNLC stages IB and IIA with high-risk of recurrence: A prospective, single-arm, phase II trial
Presenter: Yuhua Zhang
Session: Poster Display session
Resources:
Abstract
139P - Ablation combined with tislelizumab in treating hepatocellular carcinoma: A phase II trial
Presenter: Yangxun Pan
Session: Poster Display session
Resources:
Abstract
140P - Tislelizumab combined with lenvatinib and transarterial chemoembolization(TACE) neoadjuvant treatment in resectable CNLC IIa-IIb hepatocellular carcinoma: A prospective, single-arm, phase II study
Presenter: Zhibo Zhang
Session: Poster Display session
Resources:
Abstract
141P - Efficacy and safety of tislelizumab(T) combined with gemcitabine and cisplatin(GC) for patients with localized muscle-invasive bladder cancer(MIBC) after radical local surgery: A prospective, phase II study
Presenter: Ming Cao
Session: Poster Display session
Resources:
Abstract
143P - Strength of patient (pt) preference for atezolizumab (atezo) subcutaneous (SC) vs intravenous (IV) for the treatment of NSCLC: exploratory analyses from the IMscin002 study
Presenter: Margarita Majem Tarruella
Session: Poster Display session
Resources:
Abstract
144P - First-line cemiplimab monotherapy for advanced non-small cell lung cancer (NSCLC) of squamous histology: Subgroup analysis with 5-year results from EMPOWER-Lung 1
Presenter: Tamta Makharadze
Session: Poster Display session
Resources:
Abstract