AI Article Synopsis

  • Immunotherapy is a promising cancer treatment, but only a few patients respond, highlighting the need for better biomarkers.
  • This study introduces PathwayTMB, a new method that identifies genomic mutation pathways to predict immunotherapy outcomes by calculating a pathway-based tumor mutational burden (PTMB).
  • In tests with melanoma patients, those with high immune-related prognostic signatures (IPSP) had longer survival and better treatment responses, and the IPSP proved more effective than traditional tumor mutational burden measures.
  • The findings suggest that PathwayTMB could be a valuable tool for predicting success in immunotherapy, particularly for immune checkpoint inhibitors across various cancers.

Article Abstract

Immunotherapy has become one of the most promising therapy methods for cancer, but only a small number of patients are responsive to it, indicating that more effective biomarkers are urgently needed. This study developed a pathway analysis method, named PathwayTMB, to identify genomic mutation pathways that serve as potential biomarkers for predicting the clinical outcome of immunotherapy. PathwayTMB first calculates the patient-specific pathway-based tumor mutational burden (PTMB) to reflect the cumulative extent of mutations for each pathway. It then screens mutated survival benefit-related pathways to construct an immune-related prognostic signature based on PTMB (IPSP). In a melanoma training set, IPSP-high patients presented a longer overall survival and a higher response rate than IPSP-low patients. Moreover, the IPSP showed a superior predictive effect compared with TMB. In addition, the prognostic and predictive value of the IPSP was consistently validated in two independent validation sets. Finally, in a multi-cancer dataset, PathwayTMB also exhibited good performance. Our results indicate that PathwayTMB could identify the mutation pathways for predicting immunotherapeutic survival, and their combination may serve as a potential predictive biomarker for immune checkpoint inhibitor therapy.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10514137PMC
http://dx.doi.org/10.1016/j.omtn.2023.09.003DOI Listing

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