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(18)F-FDG-PET/CT in evaluating response to therapy in solid tumors: where we are and where we can go
K Herrmann1, M R Benz, B J Krause
1Departments of Molecular and Medical Pharmacology, Ahmanson Translational Imaging Division, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA 90095-1782, USA. kherrmann@mednet.ucla.edu
Abstract:
In the past, enormous public and private investments have been made to reduce cancer incidence and mortality. Despite some improvements over the last 10 years, the overall outcome of the "war on cancer" has been disappointing. Among the reasons for this limited success is our inability to determine, whether the therapeutic target is present, and whether the target is reached by the drug. A further important issue is our limited ability to correctly assess response to treatment early after start of therapy which would allow for more individualized treatment approaches. PET and PET/CT with the glucose analogue 2'-[(18)F]-fluoro-2'-deoxy-D-glucose (FDG) are increasingly used to assess response to therapy in patients, and a converging large body of evidence is emerging that suggests that changes in glucose utilization during therapy can be used to predict clinical outcome. In this article we provide an overview of the utility of (18)F-FDG PET/CT imaging for early monitoring of cancer therapy and address current and future challenges for its more widespread adoption. First, we discuss general requirements that any imaging modality must meet to provide valid and valuable treatment response assessment. We will then review the strengths and limitations of CT (RECIST) and PET based response criteria. Finally, we will examine the role of FDG-PET/(CT) imaging for response assessments in solid tumors.
Insights
Early cancer treatment monitoring using 18F-FDG PET/CT shows promise. This imaging technique assesses changes in glucose metabolism to predict patient outcomes, aiding personalized cancer therapy.
Area of Science:
- Oncology
- Nuclear Medicine
- Radiology
Background:
- Despite significant investments, the "war on cancer" has yielded disappointing results.
- Limited ability to assess therapeutic target presence, drug delivery, and early treatment response hinders personalized cancer care.
- Current methods struggle to provide timely and accurate assessments of treatment efficacy.
Purpose of the Study:
- To provide an overview of 18F-FDG PET/CT imaging for early cancer therapy monitoring.
- To discuss the utility of assessing changes in glucose utilization for predicting clinical outcomes.
- To address challenges and requirements for widespread adoption of FDG-PET/CT in cancer treatment assessment.
Main Methods:
- Review of general requirements for imaging modalities in treatment response assessment.
- Evaluation of the strengths and limitations of CT-based criteria (RECIST) and PET-based response criteria.
- Examination of the role of 18F-FDG PET/CT imaging in assessing response in solid tumors.
Main Results:
- Emerging evidence suggests changes in glucose utilization during therapy, as measured by FDG-PET/CT, can predict clinical outcomes.
- FDG-PET/CT offers a valuable tool for early monitoring of cancer therapy response.
- Comparison of CT (RECIST) and PET-based response criteria highlights the potential of FDG-PET/CT.
Conclusions:
- 18F-FDG PET/CT imaging is a promising modality for early cancer therapy monitoring.
- Assessing metabolic changes via FDG-PET/CT can guide individualized treatment approaches.
- Further adoption of FDG-PET/CT requires addressing current challenges and establishing standardized criteria.
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