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Updated: May 27, 2026

A Novel High-resolution In vivo Imaging Technique to Study the Dynamic Response of Intracranial Structures to Tumor Growth and Therapeutics
Published on: June 16, 2013
Novel oncologic drugs: what they do and how they affect images
Roberto García Figueiras1, Anwar R Padhani, Vicky J Goh
1Department of Radiology, Grupo de Imagen Molecular, Fundación IDICHUS/IDIS, Complexo Hospitalario Universitario de Santiago de Compostela, Choupana s/n, 15702 Santiago de Compostela, Spain. roberto.garcia.figueiras@sergas.es
Abstract:
Targeted therapies are designed to interfere with specific aberrant biologic pathways involved in tumor development. The main classes of novel oncologic drugs include antiangiogenic drugs, antivascular agents, drugs interfering with EGFR-HER2 or KIT receptors, inhibitors of the PI3K/Akt/mTOR pathway, and hormonal therapies. Cancer cells usurp normal signal transduction pathways used by growth factors to stimulate proliferation and sustain viability. The interaction of growth factors with their receptors activates different intracellular pathways affecting key tumor biologic processes such as neoangiogenesis, tumor metabolism, and tumor proliferation. The response of tumors to anticancer therapy can be evaluated with anatomic response assessment, qualitative response assessment, and response assessment with functional and molecular imaging. Angiogenesis can be measured by means of perfusion imaging with computed tomography and magnetic resonance (MR) imaging. Diffusion-weighted MR imaging allows imaging evaluation of tumor cellularity. The main imaging techniques for studying tumor metabolism in vivo are positron emission tomography and MR spectroscopy. Familiarity with imaging findings secondary to tumor response to targeted therapies may help the radiologist better assist the clinician in accurate evaluation of tumor response to these anticancer treatments. Functional and molecular imaging techniques may provide valuable data and augment conventional assessment of tumor response to targeted therapies. Supplemental material available at http://radiographics.rsna.org/lookup/suppl/doi:10.1148/rg.317115108/-/DC1.
Insights
Targeted cancer therapies disrupt tumor growth pathways. Advanced imaging techniques like perfusion CT, diffusion-weighted MRI, and PET scans help assess treatment response by evaluating tumor angiogenesis, cellularity, and metabolism.
Area of Science:
- Oncology
- Radiology
- Molecular Imaging
Background:
- Targeted therapies aim to disrupt specific aberrant biologic pathways crucial for tumor development.
- Cancer cells exploit normal growth factor signaling pathways to promote proliferation and survival.
- Novel oncologic drugs include antiangiogenic agents, antivascular agents, receptor inhibitors (EGFR-HER2, KIT), PI3K/Akt/mTOR pathway inhibitors, and hormonal therapies.
Purpose of the Study:
- To review the role of functional and molecular imaging in evaluating tumor response to targeted therapies.
- To familiarize radiologists with imaging findings associated with targeted therapy response.
- To highlight how advanced imaging can augment conventional tumor response assessment.
Main Methods:
- Review of current literature on targeted therapies and their impact on tumor biology.
- Discussion of various imaging modalities used to assess tumor response.
- Specific mention of perfusion imaging (CT, MRI) for angiogenesis, diffusion-weighted MRI for cellularity, and PET/MR spectroscopy for metabolism.
Main Results:
- Targeted therapies interfere with key tumor processes like neoangiogenesis, metabolism, and proliferation.
- Anatomic, qualitative, and functional/molecular imaging are used to assess treatment response.
- Perfusion imaging, diffusion-weighted MRI, PET, and MR spectroscopy offer insights into tumor response.
Conclusions:
- Familiarity with imaging findings of targeted therapy response is essential for accurate clinical assessment.
- Functional and molecular imaging provide valuable data to supplement conventional response evaluation.
- Radiologists play a key role in assisting clinicians by accurately evaluating tumor response to targeted anticancer treatments.
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