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Imaging EGFR and HER2 by PET and SPECT: a review
Emily B Corcoran1, Robert N Hanson
1Department of Chemistry and Chemical Biology, Northeastern University, 360 Huntington Avenue, Boston, Massachusetts.
Abstract:
In an effort to discover a noninvasive method for predicting which cancer patients will benefit from therapy targeting the EGFR and HER2 proteins, a large body of the research has been conducted toward the development of PET and SPECT imaging agents, which selectively target these receptors. We provide a general overview of the advances made toward imaging EGFR and HER2, detailing the investigation of PET and SPECT imaging agents ranging in size from small molecules to monoclonal antibodies.
Insights
Researchers are developing noninvasive imaging agents for Positron Emission Tomography (PET) and Single-Photon Emission Computed Tomography (SPECT) to predict cancer patient response to EGFR and HER2 therapies.
Area of Science:
- Oncology
- Radiochemistry
- Molecular Imaging
Background:
- Targeted therapies for cancer often focus on Epidermal Growth Factor Receptor (EGFR) and Human Epidermal growth factor Receptor 2 (HER2) proteins.
- Predicting patient response to these therapies noninvasively is a significant clinical challenge.
Purpose of the Study:
- To review advances in developing noninvasive imaging agents for predicting cancer patient response to EGFR and HER2 targeted therapies.
- To provide an overview of PET and SPECT imaging agents targeting EGFR and HER2.
Main Methods:
- Literature review of research on PET and SPECT imaging agents for EGFR and HER2.
- Discussion of various imaging agent modalities, including small molecules and monoclonal antibodies.
Main Results:
- Significant progress has been made in developing selective PET and SPECT imaging agents for EGFR and HER2.
- Investigated agents range from small molecules to large biologics like monoclonal antibodies.
Conclusions:
- Noninvasive imaging agents show promise for predicting patient response to EGFR and HER2 targeted cancer therapies.
- Continued development of PET and SPECT agents is crucial for personalized oncology.
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