Invasive pulmonary fungal infection: assessment of antifungal treatment response with intravoxel incoherent motion diffusion-weighted MR imaging
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 manifestations1. 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/mm2). 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 fitting2. 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 hypoperfusion3.

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.

Figures

Fig.1. a MR images in a 39-year-old man with favorable response to antifungal treatment. b MR images in a 29-year-old man with unfavorable response to antifungal treatment. The right curve demonstrates the signal decay curve with b values, respectively.

Fig.2 Box plots for ADC, D*, f, and D (a-d) in differentiating between patients with favorable and unfavorable response.



Proc. Intl. Soc. Mag. Reson. Med. 24 (2016)
1145