| Literature DB >> 32007223 |
Yiming Meng1, Jing Sun1, Na Qv2, Guirong Zhang1, Tao Yu3, Haozhe Piao4.
Abstract
Cancer immunotherapy, due to its high anti-tumor efficacy, has attracted considerable attention globally from experts in various fields. However, immunotherapy could be severely toxic; not all patients may respond, thus requiring combination therapy. Therefore, a reasonable selection strategy for early treatment is urgently needed. It is vital to capture the dynamic, heterogeneous, and complex tumor behavior considering the absence of ideal companion biomarkers. Since tumor immune response involves tumor cells, several other cell types, and molecules in the tumor microenvironment, detection is very complex and variable. However, molecular imaging technology, namely the non-invasive whole-body molecular imaging by positron emission tomography and single-photon emission computed tomography, has shown considerable promise in tumor detection and cancer immunotherapy response. Identification of potential novel imaging biomarkers will allow a personalized treatment plan for every patient. Future imaging strategies for these molecules used alone or in combination or continuously, might help stratify patients before or during the early stages of immunotherapy, and might address the immunotherapy challenges encountered by the oncologists.Entities:
Keywords: Cytokines; Extracellular matrix; Immune cells; Immunotherapy; Molecular imaging
Mesh:
Year: 2020 PMID: 32007223 DOI: 10.1016/j.cellimm.2020.104039
Source DB: PubMed Journal: Cell Immunol ISSN: 0008-8749 Impact factor: 4.868