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Predicting Response to Neoadjuvant Therapy in Oesophageal Adenocarcinoma

SIMPLE SUMMARY: Oesophageal adenocarcinomas are a distinct subtype of oesophageal cancer that has an increasing incidence in western countries. As these cancers are often late presenting, patients with locally advanced oesophageal adenocarcinomas are routinely treated with neoadjuvant chemotherapy w...

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Detalles Bibliográficos
Autores principales: Jiang, William, de Jong, Jelske M., van Hillegersberg, Richard, Read, Matthew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8869950/
https://www.ncbi.nlm.nih.gov/pubmed/35205743
http://dx.doi.org/10.3390/cancers14040996
Descripción
Sumario:SIMPLE SUMMARY: Oesophageal adenocarcinomas are a distinct subtype of oesophageal cancer that has an increasing incidence in western countries. As these cancers are often late presenting, patients with locally advanced oesophageal adenocarcinomas are routinely treated with neoadjuvant chemotherapy with or without radiotherapy prior to surgery. Unfortunately, this neoadjuvant protocol demonstrates limited response, while exposing patients to the side effects of therapy. Biomarkers that can accurately predict neoadjuvant therapy response would save time, suffering, hospital resources and potentially improve survival. ABSTRACT: (1) Background: Oesophageal cancers are often late-presenting and have a poor 5-year survival rate. The standard treatment of oesophageal adenocarcinomas involves neoadjuvant chemotherapy with or without radiotherapy followed by surgery. However, less than one third of patients respond to neoadjuvant therapy, thereby unnecessarily exposing patients to toxicity and deconditioning. Hence, there is an urgent need for biomarkers to predict response to neoadjuvant therapy. This review explores the current biomarker landscape. (2) Methods: MEDLINE, EMBASE and ClinicalTrial databases were searched with key words relating to “predictive biomarker”, “neoadjuvant therapy” and “oesophageal adenocarcinoma” and screened as per the inclusion and exclusion criteria. All peer-reviewed full-text articles and conference abstracts were included. (3) Results: The search yielded 548 results of which 71 full-texts, conference abstracts and clinical trials were eligible for review. A total of 242 duplicates were removed, 191 articles were screened out, and 44 articles were excluded. (4) Discussion: Biomarkers were discussed in seven categories including imaging, epigenetic, genetic, protein, immunologic, blood and serum-based with remaining studies grouped in a miscellaneous category. (5) Conclusion: Although promising markers and novel methods have emerged, current biomarkers lack sufficient evidence to support clinical application. Novel approaches have been recommended to assess predictive potential more efficiently.