Purpose: In tumour, the imbalance between oxygen supply and demand leads to hypoxia, which represents a negative prognostic factor associated with aggressive tumour phenotype and therapy resistance. This review provides an overview of the use of positron emitter-labelled radiopharmaceutical used to image hypoxia in preclinical models of cancer. Methods: A critical and comprehensive PubMed search was performed identifying articles related to PET imaging for hypoxia assessment in preclinical setting from January 2007 up to January 2017. Results: We have considered and described a total of 54 original articles, exploring tumour-associated hypoxia in preclinical models. Results underlined the potential application together with the advantages and pitfalls of the use of PET in preclinical research. Multi-target imaging allowed to better define the relationship between hypoxia and other biological hallmarks of tumour; imaging of hypoxia was proved as a useful tool for lesions stratification and response prediction to radiotherapy; however, cutoff indexes were identified in few studies. Hypoxia PET showed remarkable tracer delivery limitations in the study of vascular disrupting agents but suggested the potential use of PET as a marker of response or resistance to anti-angiogenics. Finally, the effect of anaesthesia on tracer kinetics and tumour oxygenation as well as perfusion dependency in tracer uptake should be carefully evaluated to avoid artefactual results. Conclusions: Preclinical studies highlight the advantages and the limitations of the available hypoxia-radiotracers and their potential usefulness for the evaluation of treatments outcome and radiotherapy planning

Raccagni, I., Valtorta, S., Moresco, R., Belloli, S. (2017). Tumour hypoxia: lessons learnt from preclinical imaging. CLINICAL AND TRANSLATIONAL IMAGING, 5(5), 407-425 [10.1007/s40336-017-0248-5].

Tumour hypoxia: lessons learnt from preclinical imaging

RACCAGNI, ISABELLA
Primo
;
VALTORTA, SILVIA
Secondo
;
MORESCO, ROSA MARIA
Penultimo
;
BELLOLI, SARA
Ultimo
2017

Abstract

Purpose: In tumour, the imbalance between oxygen supply and demand leads to hypoxia, which represents a negative prognostic factor associated with aggressive tumour phenotype and therapy resistance. This review provides an overview of the use of positron emitter-labelled radiopharmaceutical used to image hypoxia in preclinical models of cancer. Methods: A critical and comprehensive PubMed search was performed identifying articles related to PET imaging for hypoxia assessment in preclinical setting from January 2007 up to January 2017. Results: We have considered and described a total of 54 original articles, exploring tumour-associated hypoxia in preclinical models. Results underlined the potential application together with the advantages and pitfalls of the use of PET in preclinical research. Multi-target imaging allowed to better define the relationship between hypoxia and other biological hallmarks of tumour; imaging of hypoxia was proved as a useful tool for lesions stratification and response prediction to radiotherapy; however, cutoff indexes were identified in few studies. Hypoxia PET showed remarkable tracer delivery limitations in the study of vascular disrupting agents but suggested the potential use of PET as a marker of response or resistance to anti-angiogenics. Finally, the effect of anaesthesia on tracer kinetics and tumour oxygenation as well as perfusion dependency in tracer uptake should be carefully evaluated to avoid artefactual results. Conclusions: Preclinical studies highlight the advantages and the limitations of the available hypoxia-radiotracers and their potential usefulness for the evaluation of treatments outcome and radiotherapy planning
Articolo in rivista - Review Essay
Hypoxia; Hypoxia-specific radiopharmaceuticals; PET imaging; Preclinical; Treatment outcome; Radiology, Nuclear Medicine and Imaging
English
2017
5
5
407
425
none
Raccagni, I., Valtorta, S., Moresco, R., Belloli, S. (2017). Tumour hypoxia: lessons learnt from preclinical imaging. CLINICAL AND TRANSLATIONAL IMAGING, 5(5), 407-425 [10.1007/s40336-017-0248-5].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/171401
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