AI Article Synopsis

  • Targeted therapy in metastatic melanoma can significantly shrink tumors and improve long-term survival by triggering immune responses through antigen release.
  • Blood samples from 19 patients undergoing this treatment were analyzed to identify gene expression changes, showing that certain genes were activated while others were inhibited during treatment.
  • Despite poorer clinical characteristics in patients compared to earlier studies, the radiological response rates were comparable, indicating the potential for gene expression patterns to serve as biomarkers for immune responses and guide future combination therapies.

Article Abstract

Targeted therapy in metastatic melanoma often achieves a major tumour regression response and significant long-term survival via the release of antigens that reinduce immunocompetence. The biomarkers thus activated may guide the prediction of response, but this association and its mechanism have yet to be established. Blood samples were collected from nineteen consecutive patients with metastatic melanoma before, during, and after treatment with targeted therapy. Differential gene expression analysis was performed, which identified the genes involved in the treatment, both in the first evaluation of response and during progression. Although clinical characteristics of the patients were poorer than those obtained in pivotal studies, radiological responses were similar to those reported previously (objective response rate: 73.7%). In the first tumour assessment, the expression of some genes increased (CXCL-10, SERPING1, PDL1, and PDL2), while that of others decreased (ARG1, IL18R1, IL18RAP, IL1R1, ILR2, FLT3, SLC11A1, CD163, and S100A12). The analysis of gene expression in blood shows that some are activated and others inhibited by targeted therapy. This response pattern may provide biomarkers of the immune reinduction response, which could be used to study potential combination treatments. Nevertheless, further studies are needed to validate these results.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8869294PMC
http://dx.doi.org/10.3390/biomedicines10020284DOI Listing

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