Oops, you're using an old version of your browser so some of the features on this page may not be displaying properly.

MINIMAL Requirements: Google Chrome 24+Mozilla Firefox 20+Internet Explorer 11Opera 15–18Apple Safari 7SeaMonkey 2.15-2.23

Cocktail & Poster Display session

98P - Clinical implementation of NGS and ESCAT for optimized cancer therapy

Date

16 Oct 2024

Session

Cocktail & Poster Display session

Presenters

AI. Martin-Quesada

Citation

Annals of Oncology (2024) 9 (suppl_6): 1-5. 10.1016/esmoop/esmoop103742

Authors

A. Martin-Quesada1, A. Herrero Márquez2, C. Dorta Pérez3, A. Rosa Díaz4, P. Rodriguez3, L. Herrera Gorrìn5, M. Morales-Gonzalez3, M. Fuentes Ferrer6, A. Cardena7

Author affiliations

  • 1 Cell Therapy And Early Drug Development Unit, Medical Oncology Department, CHUV - Centre Hospitalier Universitaire Vaudois, 1010 - Lausanne/CH
  • 2 Oncology Dept., Hospital Universitario Nuestra Senora de Candelaria, 38010 - Santa Cruz de Tenerife/ES
  • 3 Medical Oncology Department, Hospital Universitario Nuestra Senora de Candelaria, 38010 - Santa Cruz de Tenerife/ES
  • 4 Medical Oncology Dept., Hospital Universitario Nuestra Senora de Candelaria, 38010 - Santa Cruz de Tenerife/ES
  • 5 Oncología Médica, Universidad de La Laguna, 38200 - San Cristobal de la Laguna/ES
  • 6 Research Unit, Hospital Universitario Nuestra Señora de Candelaria, 38010 - Santa Cruz de Tenerife/ES
  • 7 Dept. Oncology, Hospital Universitario Nuestra Senora de Candelaria, 38010 - Santa Cruz de Tenerife/ES

Resources

This content is available to ESMO members and event participants.

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.

This site uses cookies. Some of these cookies are essential, while others help us improve your experience by providing insights into how the site is being used.

For more detailed information on the cookies we use, please check our Privacy Policy.

Customise settings
  • Necessary cookies enable core functionality. The website cannot function properly without these cookies, and you can only disable them by changing your browser preferences.