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Novel Biomarkers and Druggable Targets in Advanced Melanoma. | LitMetric

Novel Biomarkers and Druggable Targets in Advanced Melanoma.

Cancers (Basel)

Department of Hemato-Oncology, European Institute of Oncology IRCCS, 20141 Milan, Italy.

Published: December 2021

AI Article Synopsis

  • Immunotherapy and targeted therapies like Ipilimumab and BRAF-inhibitors have revolutionized melanoma treatment, offering cures or long-term survival for many patients.
  • Despite these advancements, about 50% of patients with advanced disease do not benefit significantly, and predicting patient responses or side effects remains challenging for clinicians.
  • The manuscript discusses various potential biomarkers in four categories (molecular, immunological, peripheral, and gut microbiota) that could help personalize treatment plans and improve predictions for patient responses and toxicities.

Article Abstract

Immunotherapy with Ipilimumab or antibodies against programmed death (ligand) 1 (anti-PD1/PDL1), targeted therapies with BRAF-inhibitors (anti-BRAF) and their combinations significantly changed melanoma treatment options in both primary, adjuvant and metastatic setting, allowing for a cure, or at least long-term survival, in most patients. However, up to 50% of those with advance or metastatic disease still have no significant benefit from such innovative therapies, and clinicians are not able to discriminate in advance neither who is going to respond and for how long nor who is going to develop collateral effects and which ones. However, druggable targets, as well as affordable and reliable biomarkers are needed to personalize resources at a single-patient level. In this manuscript, different molecules, genes, cells, pathways and even combinatorial algorithms or scores are included in four biomarker chapters (molecular, immunological, peripheral and gut microbiota) and reviewed in order to evaluate their role in indicating a patient's possible response to treatment or development of toxicities.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8750474PMC
http://dx.doi.org/10.3390/cancers14010081DOI Listing

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