Chenggong Yan1, Jun Xu2, Wei Xiong1, Qi Wei2, Yingjie Mei3, and Yikai Xu1
1Department of Medical Imaing Center, Nanfang Hospital, Southern Medical Univeristy, Guangzhou, Guangdong Province, China, People's Republic of, 2Department of Hematology, Nanfang Hospital, Southern Medical University, Guangzhou, China, People's Republic of, 3Philips Healthcare, Guangzhou, China, People's Republic of
Synopsis
In this study,
we
evaluate the diffusion
and perfusion characteristics of pulmonary invasive fungal infections (IFI), which
were calculated
using the intravoxel
incoherent motion
(IVIM) model. We found that a low perfusion fraction f might be a noninvasive imaging biomarker for unfavorable
response.Purpose
Invasive fungal
infection (IFI) has emerged as an important cause of life-threatening
opportunistic respiratory complication in severely immunocompromised patients. Early
recognition of IFI indicating clinical outcome may be important for decisions
concerning the strategy and duration of antifungal treatment, surgical
intervention, and monitoring fungal manifestations
1. However,
critical gaps in knowledge remain regarding diagnostic tools for assessing response
to facilitate proper management of these infections. The purpose of this study
was to determine whether intravoxel incoherent motion (IVIM) –derived
parameters and apparent diffusion coefficient (ADC) could act as imaging
biomarkers for predicting antifungal treatment response.
Methods
This study was approved by the local ethics committee and
informed consent was obtained from all participants. Forty-six consecutive
patients (mean age, 33.9 ± 13.0 y) with newly diagnosed IFI in the lung
according to ORTC/MSG criteria were prospectively enrolled. All patients underwent
diffusion-weighted magnetic resonance (MR) imaging at 3.0 T MR scanner (Achieva
TX, Philips Healthcare, Best, Netherlands) using 11 b values (0, 20, 50, 80, 110,
150, 200, 400, 600, 800, 1000 sec/mm
2). Scanning parameters were as follows:
TR/TE= 2100/55 ms, FOV= 375 mm × 300 mm; NEX= 2; slice thickness= 5 mm. A
bi-exponential signal decay can be obtained and the two-step method was
used for voxel wise fitting
2. Pseudodiffusion coffiecient D*, perfusion fraction f,
and the diffusion coefficient D were calculated using the IVIM model. ADC was calculated using a mono-exponential model. A
freehand region of interest (ROI) was manually outlined the largest pulmonary
IFI lesion on ADC and IVIM parametric maps. Patients were stratified into favorable
(n=32) and unfavorable response (n=14) groups based on follow-up for
determination of the predictive powers of IVIM parameters using Student t test
and receiver operating characteristic (ROC) curve analyses.
Results
DWI signal decay curves in favorable
response group were found to be biexponential fit in comparison with the
monoexponential fit for the unfavorable response group (Fig.1). D was
consistently lower than ADC in all tissues. f values were significantly lower
in the unfavorable response group (12.6%±4.4%) than in the favorable response group (30.2%±8.6%) (Z=4.989, P<0.001). However, the ADCtotal,
D, and D* were not significantly different between the two groups (P>0.05,
Fig.2). Receiver operating characteristic curve analyses showed f to be a
significant predictor for differentiation(AUC=0.967), with a sensitivity of 93.8%
and a specificity of 92.9%.
Discussion
In the present study, we attempted to validate the
IVIM-derived perfusion and diffusion parameters to predict antifungal treatment
response. Our study clarified the different perfusion characteristics of IFI
lesions with favorable response and unfavorable response on the basis of the
IVIM biexponential model. We found that the obtained f value was significantly lower
in patients with unfavorable response than in those with favorable response,
suggesting that f may be a biomarker for prediction of antifungal treatment. In
this work, the decrease of f in patients with unfavorable response may well be
caused by invasion of large pulmonary arteries and thrombosis formation in the IFI
area as well as by concordant hypoperfusion
3.
Acknowledgements
No acknowledgement found.References
1.
Karthaus M,
Buchheidt D. Invasive aspergillosis: new insights into disease, diagnostic and
treatment. Curr Pharm Des. 2013;19:3569-3594.
2.
Lee EY, Yu X, Chu
MM, et al. Perfusion and diffusion characteristics of cervical cancer based on
intraxovel incoherent motion MR imaging-a pilot study. Eur Radiol. 2014;24:1506-1513.
3. Smith JA, Kauffman
CA. Pulmonary fungal infections. Respirology. 2012; 17:913-926.