Apparent transverse relaxation (R*2) on MRI as a method to differentiate treatment effect (pseudoprogression) versus progressive disease in chemoradiation for malignant glioma

被引:6
作者
Belliveau, Jean-Guy [1 ,2 ]
Bauman, Glenn S. [1 ,3 ,4 ]
Macdonald, David [3 ,4 ]
Macdonald, Maria [3 ,4 ]
Klassen, L. Martyn [2 ]
Menon, Ravi S. [1 ,2 ]
机构
[1] Univ Western Ontario, Dept Med Biophys, London, ON, Canada
[2] Univ Western Ontario, Robarts Res Inst, Ctr Funct & Metab Mapping, London, ON, Canada
[3] Univ Western Ontario, Dept Oncol, London, ON, Canada
[4] London Reg Canc Program, London, ON, Canada
基金
加拿大创新基金会;
关键词
concurrent chemoradiotherapy; glioma; progression; pseudoprogression; R-2*; SUSCEPTIBILITY MAPPING QSM; HIGH-GRADE GLIOMAS; ADJUVANT TEMOZOLOMIDE; GLIOBLASTOMA; RADIOTHERAPY; CONCOMITANT; CRITERIA; TUMORS; PHASE; DIFFUSION;
D O I
10.1111/1754-9485.12694
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
IntroductionPseudoprogression (psPD) is a transient post-treatment imaging change that is commonly seen when treating glioma with chemotherapy and radiation. The use of apparent transverse relaxation rate (R2), which is calculated from a contrast-free multi-echo gradient echo Magnetic Resonance Imaging (MRI) sequence, may allow for quantitative identification of patients with suspected psPD. MethodsWe acquired a multi-echo gradient echo sequence using a 3T-Siemens Prisma MRI. The signal decay through the echoes was fitted to provide the R2 coefficient. We segmented the T-1-gadolinium enhancing the image to provide a contrast enhancing lesion (CEL) and the FLAIR hyperintensity to provide a non-enhancing lesion (NEL). These regions of interest were applied to the multi-echo gradient echo to acquire a mean R2 within the CEL and NEL. We additionally acquired ADC data to attempt to corroborate our findings. ResultsWe found that patients who later exhibited PD exhibited a higher R2 within the CEL as well as a higher ratio of CEL to NEL. Our data correctly distinguished pseudoprogression from treatment effect in 9/9 patients, while ADC corrected identified 7/9 patients using an absolute ADC of 1200x10(-6)mm(2)/s. ConclusionsOur method seems promising for the accurate identification of psPD, and the technique is amenable to evaluation in larger, multi-centre patient cohorts.
引用
收藏
页码:224 / 231
页数:8
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