Peptide Based Imaging Agents for HER2 Imaging in Oncology.
Maxwell DucharmeSuzanne E LapiPublished in: Molecular imaging (2021)
Breast cancer continues to be the most lethal cancer type in women and one of the most diagnosed. Understanding Breast cancer receptor status is one of the most vital processes for determining treatment options. One type of breast cancer, human epidermal growth factor receptor 2 (HER2) positive, has approved receptor-based therapies including trastuzumab and pertuzumab that can significantly increase the likelihood of survival. Current methods to determine HER2 status include biopsies with immunohistochemical staining and/or fluorescence in situ hybridization. However, positron emission tomography (PET) imaging techniques using 89Zr-trastuzumab or 89Zr-pertuzumab are currently in clinical trials for a non-invasive, full body diagnostic approach. Although the antibodies have strong specificity to the HER2 positive lesions, challenges involving long post-injection time for imaging due to the blood circulation of the antibodies and matching of long-live isotopes leading to increased dose to the patient leave opportunities for alternative PET imaging probes. Peptides have been shown to allow for shorter injection-to-imaging time and can be used with shorter lived isotopes. HER2 specific peptides under development will help improve the diagnosis and potentially therapy options for HER2 positive breast cancer. Peptides showing specificity for HER2 could start widespread development of molecular imaging techniques for HER2 positive cancers.
Keyphrases
- pet imaging
- epidermal growth factor receptor
- positron emission tomography
- high resolution
- clinical trial
- computed tomography
- advanced non small cell lung cancer
- tyrosine kinase
- randomized controlled trial
- endothelial cells
- metastatic breast cancer
- small molecule
- type diabetes
- polycystic ovary syndrome
- metabolic syndrome
- squamous cell carcinoma
- fluorescence imaging
- mesenchymal stem cells
- induced pluripotent stem cells
- skeletal muscle