New emerging targets in cancer immunotherapy: the role of neoantigens.

ESMO Open

IrsiCaixa AIDS Research Institute, Germans Trias i Pujol University Hospital, Badalona, Spain; Germans Trias i Pujol Research Institute (IGTP), Badalona, Spain; Universitat de Vic-Universitat Central de Catalunya (UVic-UCC), Vic, Spain.

Published: April 2020

AI Article Synopsis

  • Immune checkpoint inhibitors are changing how cancer is treated and are showing great results for some patients, but not for everyone.
  • New methods are needed to improve these treatments and make them safer for more people.
  • Researchers are looking into using neoantigens, which are unique to cancer cells, to create personalized vaccines and therapies that could help patients fight cancer without hurting healthy parts of their body.

Article Abstract

The success of cancer therapies with immune checkpoint inhibitors is transforming the treatment of patients with cancer and fostering cancer research. Therapies that target immune checkpoint inhibitors have shown unprecedented rates of durable long-lasting responses in patients with various cancer types, but only in a fraction of patients. Thus, novel approaches are needed to make immunotherapy more precise and also less toxic. The advances of next-generation sequencing technologies have allowed fast detection of somatic mutations in genes present in the exome of an individual tumour. Targeting neoantigens, the mutated peptides expressed only by tumour cells, may enable antitumour T-cell responses and tumour destruction without causing harm to healthy tissues. Currently, neoantigens can be identified in tumour clinical samples by using genomic-based computational tools. The two main treatment modalities targeting neoantigens that have been investigated in clinical trials are personalised vaccines and tumour infiltrating lymphocytes-based adoptive T-cell therapy. In this mini review, we discuss the promises and challenges for using neoantigens as emergent targets to personalise and guide cancer immunotherapy in a broader set of cancers.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7326255PMC
http://dx.doi.org/10.1136/esmoopen-2020-000684DOI Listing

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