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Assessment of Response to Chemotherapy and Radiotherapy

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Part of the book series: Medical Radiology ((Med Radiol Diagn Imaging))

Key Points

• The most valuable, readily available and easy-to-use techniques to assess response to radiation therapy and chemotherapy in malignant bone tumours are DCE-MR imaging, diffusion MR imaging and colour-Doppler ultrasound.

• Dynamic contrast-enhanced MR imaging allows to study the physiological effects of therapy graphically in TICs or in parametric images, that display tumour microvascularisation, perfusion, capillary permeability and volume of the interstitial space.

• There is not enough evidence to use F-18 FDG-PET routinely for monitoring therapy in bone sarcomas.

Findings indicating good response to therapy in bone sarcomas are:

• Disappearance of high systolic Doppler frequency shifts and an increased resistive index on colour-Doppler ultrasound

• Appearance of high signal intensity in bone marrow on T2-weighted images (after radiation therapy)

• Change to slow and moderate to absent enhancement on DCE-MR imaging

• Increased diffusion of water molecules with high ADC values on diffusion MR imaging

Findings indicating poor response to therapy in bone sarcomas are:

• Persistence of high systolic Doppler frequency shifts and decreased resistive index on colour-Doppler ultrasound

• Increased extent of bone marrow invasion

• Increased tumour volume or identification of a new soft tissue mass

• No decrease in the amount of peritumoral oedema

• Persistence of fast and intense enhancement on DCE-MR imaging

• Persistence of decreased diffusion of water molecules with low ADC values on diffusion MR imaging

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© 2009 Springer-Verlag Berlin Heidelberg

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Verstraete, K. (2009). Assessment of Response to Chemotherapy and Radiotherapy. In: Davies, A., Sundaram, M., James, S. (eds) Imaging of Bone Tumors and Tumor-Like Lesions. Medical Radiology. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-540-77984-1_11

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  • DOI: https://doi.org/10.1007/978-3-540-77984-1_11

  • Publisher Name: Springer, Berlin, Heidelberg

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