MRI for assessing antivascular cancer treatments
1Paul Strickland Scanner Centre, Mount Vernon Hospital, Rickmansworth Road, Northwood, Middlesex HA6 2RN, UK.
Abstract:
Selective antiangiogenesis and vascular targeting drugs hold out the promise of improved efficacy and tolerability for anticancer treatments. Early phase 1 drug trials have shown good tolerability for antiangiogenesis agents with biological activity below the maximum tolerated dose. Advanced clinical trials have demonstrated that morphological assessments of tumour response are of limited value in gauging the efficacy of treatment. MRI is a versatile technique which is sensitive to contrast mechanisms that can be affected by antivascular treatments; this use for MRI has been validated in xenografts and humans. Dynamic contrast-enhanced MRI (DCE-MRI), which demonstrates tissue perfusion and permeability, is being used clinically as a pharmacodynamic indicator of biological activity for antivascular cancer drugs. Early data show that DCE-MRI studies can define the biologically active dose and predict the efficacy of treatment on the basis of changes observed. MRI with macromolecular contrast media (MMCM) depicts microvessel permeability and fractional plasma volume. Xenograft studies with MMCM have shown great promise for evaluating antivascular treatments but this has not been used clinically. Intrinsic susceptibility-weighted MRI, which is sensitive to blood oxygenation and flow, is emerging as a technique that may be able to monitor vascular targeting therapies.
Insights
Selective antiangiogenesis drugs offer better cancer treatment. Dynamic contrast-enhanced MRI (DCE-MRI) shows biological activity and predicts treatment efficacy, guiding optimal dosing for vascular targeting therapies.
Area of Science:
- Oncology
- Radiology
- Pharmacology
Background:
- Selective antiangiogenesis and vascular targeting drugs are promising for improved anticancer efficacy and tolerability.
- Early trials show good tolerability for antiangiogenesis agents below maximum tolerated dose.
- Tumor response assessments in advanced trials have limited value in gauging treatment efficacy.
Purpose of the Study:
- To evaluate the role of MRI techniques in assessing the efficacy of antiangiogenesis and vascular targeting cancer therapies.
- To explore the potential of Dynamic Contrast-Enhanced MRI (DCE-MRI) as a pharmacodynamic indicator for antivascular drugs.
- To investigate emerging MRI techniques for monitoring vascular targeting therapies.
Main Methods:
- Review of early phase 1 and advanced clinical trials for antiangiogenesis agents.
- Validation of MRI techniques in xenografts and human studies.
- Clinical application of DCE-MRI to assess tissue perfusion and permeability.
- Exploration of MRI with macromolecular contrast media (MMCM) and intrinsic susceptibility-weighted MRI.
Main Results:
- DCE-MRI is clinically used as a pharmacodynamic indicator for antivascular cancer drugs.
- Early DCE-MRI data suggest it can define biologically active doses and predict treatment efficacy.
- MRI with MMCM shows promise in xenografts for evaluating antivascular treatments.
- Intrinsic susceptibility-weighted MRI is emerging for monitoring vascular targeting therapies.
Conclusions:
- MRI techniques, particularly DCE-MRI, are valuable tools for assessing the biological activity and predicting the efficacy of vascular targeting cancer therapies.
- DCE-MRI can help define optimal drug dosing and guide treatment decisions.
- Further clinical use of advanced MRI techniques like MMCM-MRI and susceptibility-weighted MRI is warranted for optimizing anticancer treatments.
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