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
1121P - Artificial Intelligence to predict BRAF mutational status from whole slide images in melanoma
Presenter: Céline Bossard
Session: Poster session 04
1122P - The role of imaging during follow-up after radical surgery of stage IIb-c and III cutaneous malignant melanoma: Survival results from an interim analysis of a randomized prospective multicenter study (TRIM)
Presenter: Cecilia Ladjevardi
Session: Poster session 04
1123P - Melanoma incidence and mortality decline in younger adults in Sweden: Start of a shift in the upgoing trend?
Presenter: Hildur Helgadottir
Session: Poster session 04
1124P - Adjuvant treatment of patients with stage III melanoma: 4-year follow-up time of multicenter real-world study
Presenter: Elisabeth Livingstone
Session: Poster session 04
1125P - Accuracy of PET-CT to assess extent of nodal disease in clinical stage III melanoma
Presenter: Ronen Stoff
Session: Poster session 04
1126P - A phase II study of nivolumab/relatlimab in metastatic uveal melanoma
Presenter: Jose Lutzky
Session: Poster session 04
1127P - Subgroup analysis of FOCUS phase III trial efficacy results
Presenter: Matthew Wheater
Session: Poster session 04
1128P - Preliminary results of first-in-human study of 225-Actinium MTI-201 (225Ac-MTI-201) in metastatic uveal melanoma
Presenter: Nikhil Khushalani
Session: Poster session 04
1129P - Clinical outcomes from a tebentafusp UK expanded access program in patients with metastatic uveal melanoma (mUM)
Presenter: Paul Nathan
Session: Poster session 04
1130P - Phase II trial on nivolumab plus radiotherapy in patients with metastatic mucosal melanoma: PORTER-M3 trial
Presenter: Motoo Nomura
Session: Poster session 04