TY - JOUR
T1 - The use of theranostic gadolinium-based nanoprobes to improve radiotherapy efficacy
AU - Sancey, L.
AU - Lux, F.
AU - Kotb, S.
AU - Roux, S.
AU - Dufort, S.
AU - Bianchi, A.
AU - Crémillieux, Y.
AU - Fries, P.
AU - Coll, J. L.
AU - Rodriguez-Lafrasse, C.
AU - Janier, M.
AU - Dutreix, M.
AU - Barberi-Heyob, M.
AU - Boschetti, F.
AU - Denat, F.
AU - Louis, C.
AU - Porcel, E.
AU - Lacombe, S.
AU - Le Duc, G.
AU - Deutsch, E.
AU - Perfettini, J. L.
AU - Detappe, A.
AU - Verry, C.
AU - Berbeco, R.
AU - Butterworth, K. T.
AU - McMahon, S. J.
AU - Prise, K. M.
AU - Perriat, P.
AU - Tillement, O.
N1 - Publisher Copyright:
© 2014 The Authors.
PY - 2014/9/1
Y1 - 2014/9/1
N2 - A new efficient type of gadolinium-based theranostic agent (AGuIX®) has recently been developed for MRI-guided radiotherapy (RT). These new particles consist of a polysiloxane network surrounded by a number of gadolinium chelates, usually 10. Owing to their small size (<5 nm), AGuIX typically exhibit biodistributions that are almost ideal for diagnostic and therapeutic purposes. For example, although a significant proportion of these particles accumulate in tumours, the remainder is rapidly eliminated by the renal route. In addition, in the absence of irradiation, the nanoparticles are well tolerated even at very high dose (10 times more than the dose used for mouse treatment). AGuIX particles have been proven to act as efficient radiosensitizers in a large variety of experimental in vitro scenarios, including different radioresistant cell lines, irradiation energies and radiation sources (sensitizing enhancement ratio ranging from 1.1 to 2.5). Pre-clinical studies have also demonstrated the impact of these particles on different heterotopic and orthotopic tumours, with both intratumoural or intravenous injection routes. A significant therapeutical effect has been observed in all contexts. Furthermore, MRI monitoring was proven to efficiently aid in determining a RT protocol and assessing tumour evolution following treatment. The usual theoretical models, based on energy attenuation and macroscopic dose enhancement, cannot account for all the results that have been obtained. Only theoretical models, which take into account the Auger electron cascades that occur between the different atoms constituting the particle and the related high radical concentrations in the vicinity of the particle, provide an explanation for the complex cell damage and death observed.
AB - A new efficient type of gadolinium-based theranostic agent (AGuIX®) has recently been developed for MRI-guided radiotherapy (RT). These new particles consist of a polysiloxane network surrounded by a number of gadolinium chelates, usually 10. Owing to their small size (<5 nm), AGuIX typically exhibit biodistributions that are almost ideal for diagnostic and therapeutic purposes. For example, although a significant proportion of these particles accumulate in tumours, the remainder is rapidly eliminated by the renal route. In addition, in the absence of irradiation, the nanoparticles are well tolerated even at very high dose (10 times more than the dose used for mouse treatment). AGuIX particles have been proven to act as efficient radiosensitizers in a large variety of experimental in vitro scenarios, including different radioresistant cell lines, irradiation energies and radiation sources (sensitizing enhancement ratio ranging from 1.1 to 2.5). Pre-clinical studies have also demonstrated the impact of these particles on different heterotopic and orthotopic tumours, with both intratumoural or intravenous injection routes. A significant therapeutical effect has been observed in all contexts. Furthermore, MRI monitoring was proven to efficiently aid in determining a RT protocol and assessing tumour evolution following treatment. The usual theoretical models, based on energy attenuation and macroscopic dose enhancement, cannot account for all the results that have been obtained. Only theoretical models, which take into account the Auger electron cascades that occur between the different atoms constituting the particle and the related high radical concentrations in the vicinity of the particle, provide an explanation for the complex cell damage and death observed.
UR - http://www.scopus.com/inward/record.url?scp=84907486504&partnerID=8YFLogxK
U2 - 10.1259/bjr.20140134
DO - 10.1259/bjr.20140134
M3 - Review article
C2 - 24990037
AN - SCOPUS:84907486504
SN - 0007-1285
VL - 87
JO - British Journal of Radiology
JF - British Journal of Radiology
IS - 1041
M1 - 20140134
ER -