Abstract 98P
Background
Advances in next-generation sequencing (NGS) make possible the selection of highly targeted therapies based on a tumour's genetic profile, resulting in better outcomes with a potential impact on progression-free survival and overall survival (Bewicke-Copley F, 2019; Gibbs SN, 2023; Coquerelle S, 2020). Moreover, it seems to be a cost-effective test (Pruneri G, 2021). ESMO Scale of Actionability of molecular Targets (ESCAT) aids in evaluating treatment efficacy, emphasizing the promise of personalized medicine in cancer care (Mateo J, 2018; Mosele F, 2020; Mosele F, 2024). Therefore, we decided to review the experience of the test in our center together with the ESCAT.
Methods
A retrospective observational study was carried out with cancer patients who had undergone a NGS test from January 2017 to December 2023 in the Medical Oncology Service of our hospital. The study has been approved by the Ethics Committee.
Results
96 patients with a mean age of 54 years were included, 56% of whom were women. The most frequent tumours were cholangiocarcinoma (24%), colorectal cancer (16%), lung cancer (12%) and cancer of unknown primary (6%). 56% of the samples come from tissue and 100% of them were valid for examination. In 23% of cases the test was requested in the first-line setting. The mean number of tumor mutational burden and genomic alterations found was 5 respectively. The MAPK and cell-replication were the most frequently altered signalling pathways and 3% had microsatellite instability. An average of 16 clinical trials were available for these patients. 22% had actionable mutations with targeted therapy and tumor-specific evidence and 24% exhibited mutations but with evidence-based treatments for other tumour types. 34% of patients received treatment based on NGS results after the test, while 8% received it but in later treatment lines. 49% had a favourable ESCAT classification (I-II).
Conclusions
In our clinical experience the NGS test should be implemented in routine clinical practice for decision making. In order to benefit from the test, patients should be selected according to ESMO guidelines. ESCAT is a useful instrument to exploit. Prospective studies should be performed with a more homogeneous population to assess the impact of the NGS test and the ESCAT.
Editorial acknowledgement
Clinical trial identification
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
163TiP - Single-institution, single-arm, open-label phase II basket study of mutation and/or elevated hedgehog (Hh) expression-directed smoothened inhibitor sonidegib in patients with advanced solid malignancies
Presenter: Madhawa De Silva
Session: Cocktail & Poster Display session
Resources:
Abstract
164TiP - MONSTAR-GLYCO: A multi-institutional prospective study harnessing glycomics and multi-omics on the j-glyconet and SCRUM-MONSTR platform
Presenter: Tadayoshi Hashimoto
Session: Cocktail & Poster Display session
Resources:
Abstract
166P - Unravelling HR-positive, HER2-negative breast cancer and its tumor microenvironment heterogeneity using spatial transcriptomics
Presenter: Bengisu Karakose
Session: Cocktail & Poster Display session
Resources:
Abstract
167P - Cancer neutrophil encyclopedia: A deep dive into antigen-presenting warriors
Presenter: Yingcheng Wu
Session: Cocktail & Poster Display session
Resources:
Abstract
168P - Tumor microenvironment (TME) and PD-L1 expression heterogeneity in high grade serous ovarian cancer (HGSC) samples analysis from the randomized NeoPembrOV/GINECO phase II trial
Presenter: Laetitia Collet
Session: Cocktail & Poster Display session
Resources:
Abstract
169P - Tumour microenvironment in glioblastoma: A single-cell perspective on macrophage dynamics and T cell exhaustion
Presenter: Farasat Kazmi
Session: Cocktail & Poster Display session
Resources:
Abstract
170P - Digital spatial profiling to uncover biomarkers for response prediction in locally advanced gastric cancer patients treated with neoadjuvant chemotherapy
Presenter: Chiara Molinari
Session: Cocktail & Poster Display session
Resources:
Abstract
171P - Immune-modulatory drug profiling using perfused, microfluidic on-chip co-cultures of patient-derived ovarian cancer microtumors and autologous immune cells
Presenter: Sarah Plöger
Session: Cocktail & Poster Display session
Resources:
Abstract
172P - The impact of androgen ablation on the immune landscape in therapy-resistant prostate cancer: Insights from tumour microenvironment analysis
Presenter: Jodi Stewart
Session: Cocktail & Poster Display session
Resources:
Abstract
173P - NRF2 levels in high grade serous ovarian cancer: Characterization and treatment
Presenter: Helen Toma
Session: Cocktail & Poster Display session
Resources:
Abstract