» Articles » PMID: 39409968

The Role of Liquid Biopsy in Gastroenteropancreatic Neuroendocrine Neoplasms

Overview
Journal Cancers (Basel)
Publisher MDPI
Specialty Oncology
Date 2024 Oct 16
PMID 39409968
Authors
Affiliations
Soon will be listed here.
Abstract

Neuroendocrine neoplasms incidence has been increasing, arising the need for precise and early diagnostic tools. Liquid biopsy (LB) offers a less invasive alternative to tissue biopsy, providing real-time molecular information from circulating tumour components in body fluids. The aim of this review is to analyse the current evidence concerning LB in NENs and its role in clinical practice. We conducted a systematic review in July 2024 focusing on LB applications in NENs, including circulating tumour cells (CTCs), circulating tumour DNA (ctDNA), micro RNA (miRNA), messenger RNA (mRNA) and extracellular vesicles. Sixty-five relevant articles were analysed. The LB showed potential in diagnosing and monitoring NENs. While CTCs face limitations due to low shedding, ctDNA provides valuable information on high-grade neoplasms. MiRNA and mRNA (e.g., the NETest) offer high sensitivity and specificity for diagnosis and prognosis, outperforming traditional markers like chromogranin A. The LB has significant potential for NEN diagnosis and monitoring but lacks widespread clinical integration due to limited prospective studies and guidelines, requiring further validation. Advances in sequencing technologies may enhance the clinical utility of LB in NENs. Future research should focus on refining LB methods, standardising protocols and exploring applications in high-grade NENs.

Citing Articles

NETest and Gastro-Entero-Pancreatic Neuroendocrine Tumors: Still Far from Routine Clinical Application? A Systematic Review.

Rossi R, La Salvia A Genes (Basel). 2025; 16(2).

PMID: 40004490 PMC: 11855739. DOI: 10.3390/genes16020161.

References
1.
Sorbye H, Hjortland G, Vestermark L, Sundlov A, Assmus J, Couvelard A . NETest in advanced high-grade gastroenteropancreatic neuroendocrine neoplasms. J Neuroendocrinol. 2024; 36(11):e13428. DOI: 10.1111/jne.13428. View

2.
Jayaprakasam V, Bodei L . Neuroendocrine Tumor Therapy Response Assessment. PET Clin. 2023; 18(2):267-286. DOI: 10.1016/j.cpet.2022.11.009. View

3.
Barriuso J, Custodio A, Afonso R, Alonso V, Astudillo A, Capdevila J . Prognostic and predictive biomarkers for somatostatin analogs, peptide receptor radionuclide therapy and serotonin pathway targets in neuroendocrine tumours. Cancer Treat Rev. 2018; 70:209-222. DOI: 10.1016/j.ctrv.2018.09.008. View

4.
Dasari A, Morris V, Allegra C, Atreya C, Benson 3rd A, Boland P . ctDNA applications and integration in colorectal cancer: an NCI Colon and Rectal-Anal Task Forces whitepaper. Nat Rev Clin Oncol. 2020; 17(12):757-770. PMC: 7790747. DOI: 10.1038/s41571-020-0392-0. View

5.
Modlin I, Drozdov I, Kidd M . The identification of gut neuroendocrine tumor disease by multiple synchronous transcript analysis in blood. PLoS One. 2013; 8(5):e63364. PMC: 3655166. DOI: 10.1371/journal.pone.0063364. View