TY - JOUR
T1 - Delayed contrast extravasation MRI
T2 - A new paradigm in neuro-oncology
AU - Zach, Leor
AU - Guez, David
AU - Last, David
AU - Daniels, Dianne
AU - Grober, Yuval
AU - Nissim, Ouzi
AU - Hoffmann, Chen
AU - Nass, Dvora
AU - Talianski, Alisa
AU - Spiegelmann, Roberto
AU - Tsarfaty, Galia
AU - Salomon, Sharona
AU - Hadani, Moshe
AU - Kanner, Andrew
AU - Blumenthal, Deborah T.
AU - Bukstein, Felix
AU - Yalon, Michal
AU - Zauberman, Jacob
AU - Roth, Jonathan
AU - Shoshan, Yigal
AU - Fridman, Evgeniya
AU - Wygoda, Marc
AU - Limon, Dror
AU - Tzuk, Tzahala
AU - Cohen, Zvi R.
AU - Mardor, Yael
N1 - Publisher Copyright:
© The Author(s) 2014. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. All rights reserved.
PY - 2015/3
Y1 - 2015/3
N2 - Background. Conventional magnetic resonance imaging (MRI) is unable to differentiate tumor/nontumor enhancing tissues. We have applied delayed-contrast MRI for calculating high resolution treatment response assessment maps (TRAMs) clearly differentiating tumor/nontumor tissues in brain tumor patients. Methods. One hundred and fifty patients with primary/metastatic tumors were recruited and scanned by delayed-contrast MRI and perfusion MRI. Of those, 47 patients underwent resection during their participation in the study. Region of interest/threshold analysis was performed on the TRAMs and on relative cerebral blood volume maps, and correlation with histology was studied. Relative cerebral blood volume was also assessed by the study neuroradiologist. Results. Histological validation confirmed that regions of contrast agent clearance in the TRAMs >1 h post contrast injection represent active tumor, while regions of contrast accumulation represent nontumor tissues with 100% sensitivity and 92% positive predictive value to active tumor. Significant correlation was found between tumor burden in the TRAMs and histology in a subgroup of lesions resected en bloc (r2= 0.90, P<.0001). Relative cerebral blood volume yielded sensitivity/positive predictive values of 51%/96% and there was no correlation with tumor burden. The feasibility of applying the TRAMs for differentiating progression from treatment effects, depicting tumor within hemorrhages, and detecting residual tumor postsurgery is demonstrated. Conclusions. The TRAMs present a novel model-independent approach providing efficient separation between tumor/nontumor tissues by adding a short MRI scan >1 h post contrast injection. The methodology uses robust acquisition sequences, providing high resolution and easy to interpret maps with minimal sensitivity to susceptibility artifacts. The presented results provide histological validation of the TRAMs and demonstrate their potential contribution to the management of brain tumor patients.
AB - Background. Conventional magnetic resonance imaging (MRI) is unable to differentiate tumor/nontumor enhancing tissues. We have applied delayed-contrast MRI for calculating high resolution treatment response assessment maps (TRAMs) clearly differentiating tumor/nontumor tissues in brain tumor patients. Methods. One hundred and fifty patients with primary/metastatic tumors were recruited and scanned by delayed-contrast MRI and perfusion MRI. Of those, 47 patients underwent resection during their participation in the study. Region of interest/threshold analysis was performed on the TRAMs and on relative cerebral blood volume maps, and correlation with histology was studied. Relative cerebral blood volume was also assessed by the study neuroradiologist. Results. Histological validation confirmed that regions of contrast agent clearance in the TRAMs >1 h post contrast injection represent active tumor, while regions of contrast accumulation represent nontumor tissues with 100% sensitivity and 92% positive predictive value to active tumor. Significant correlation was found between tumor burden in the TRAMs and histology in a subgroup of lesions resected en bloc (r2= 0.90, P<.0001). Relative cerebral blood volume yielded sensitivity/positive predictive values of 51%/96% and there was no correlation with tumor burden. The feasibility of applying the TRAMs for differentiating progression from treatment effects, depicting tumor within hemorrhages, and detecting residual tumor postsurgery is demonstrated. Conclusions. The TRAMs present a novel model-independent approach providing efficient separation between tumor/nontumor tissues by adding a short MRI scan >1 h post contrast injection. The methodology uses robust acquisition sequences, providing high resolution and easy to interpret maps with minimal sensitivity to susceptibility artifacts. The presented results provide histological validation of the TRAMs and demonstrate their potential contribution to the management of brain tumor patients.
KW - Brain metastases
KW - Brain tumor
KW - Delayed-contrast MRI
KW - Pseudoprogression
KW - Radiation necrosis
UR - http://www.scopus.com/inward/record.url?scp=84987623230&partnerID=8YFLogxK
U2 - 10.1093/neuonc/nou230
DO - 10.1093/neuonc/nou230
M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???
C2 - 25452395
AN - SCOPUS:84987623230
SN - 1522-8517
VL - 17
SP - 457
EP - 465
JO - Neuro-Oncology
JF - Neuro-Oncology
IS - 3
ER -