Abstract 1237P
Background
LRRC15 (leucine-rich repeat containing 15) is part of the family of leucine-rich repeat proteins, and is a novel factor recently associated with aggressive cancer phenotypes. It is expressed on the cell surface, mostly in the (non-tumour) stroma of common cancers, and on a subset of lung cancer associated fibroblasts. However, in cancers of mesenchymal origin, LRRC15 is also expressed on tumour cells. Recent studies suggest a role for LRRC15 in invasion and immune modulation. The aim of this study is to understand the clinical relevance of LRRC15 expression in a lung adenocarcinoma cohort.
Methods
Tissue samples from 82 cases of early-stage lung adenocarcinoma were assessed for LRRC15 expression, along with pan-cytokeratin to distinguish tumour and stromal cells, using multiplex immunohistochemistry. Images were captured and then analysed using Zeiss Axio Scanner Z1 and Indica HALO AI image analysis platform, respectively. Tumour and stroma area were classified using Densenet v2, followed by quality control of annotated regions. Subsequently, LRRC15 expression intensity was quantified in tumour and stromal areas, and its association with 5-year survival was assessed.
Results
LRRC15 is expressed in lung adenocarcinoma with differing levels of expression across the patient cohort. Expression is more common in the stroma area, but is also observed less frequently in tumour cells. Kaplan-Meier survival analysis showed that high LRRC15 expression in stroma (non-tumour) area is associated with better 5-year survival in patients, with 67% lower risk of death (HR: 0.33, 95% CI: 0.16-0.68, P < 0.01).
Conclusions
Higher LRRC15 stromal expression in early-stage lung adenocarcinoma is indicative of better 5-year survival. LRRC15 expression in the stroma may be impacting on immune cell function to influence clinical outcome.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
University of St Andrews.
Funding
Melville Trust.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
1111P - Genomic and transcriptomic analysis of Japanese melanoma reveals candidate biomarkers for immune checkpoint inhibitor responders
Presenter: Toshihiro Kimura
Session: Poster session 04
1112P - Immunotherapy after progression to double immunotherapy: Pembrolizumab and Lenvatinib versus conventional chemotherapy for patients with metastatic melanoma after failure of PD-1/CTLA-4 inhibition
Presenter: Dimitrios Ziogas
Session: Poster session 04
1113P - A machine learning model based on computed tomography radiomics to predict prognosis in subjects with stage IV melanoma
Presenter: Maria Teresa Maccallini
Session: Poster session 04
1114P - Deciphering unresectable in-transit metastasis in melanoma: Multi-modal and longitudinal insights
Presenter: Giuseppe Tarantino
Session: Poster session 04
1115P - Multiomics clustering of patients with cutaneous melanoma to reveal survival trends based on tumor immune evasion features
Presenter: Adeliya Leleytner
Session: Poster session 04
1116P - Application of the Scottish inflammatory prognostic score to the south-east Scotland cancer network real-world melanoma cohort
Presenter: Karim El-Shakankery
Session: Poster session 04
1117P - Intratumoral microbiota is associated with prognosis in Chinese patients with skin melanoma
Presenter: Hang Jiang
Session: Poster session 04
1118P - Immunological alterations during neoadjuvant BRAF/MEK inhibition in patients with prior unresectable regionally advanced melanoma: Translational analysis from the REDUCTOR trial
Presenter: Femke Burgers
Session: Poster session 04
1119P - Genomic and transcriptomic predictors of resistance to anti-PD1 monotherapy in patients with advanced melanoma
Presenter: Wenya Wang
Session: Poster session 04
1120P - Tumoral and peripheral immunophenotype of patients with stage II/III melanoma undergoing adjuvant immunotherapy following tumor resection
Presenter: Maria Ascierto
Session: Poster session 04