Abstract

There is significant interest in whether diffusion-weighted MR imaging indices, such as the minimum apparent diffusion coefficient, may be useful clinically for preoperative tumor grading and treatment planning. To help establish the pathologic correlate of minimum ADC, we undertook a study investigating the relationship between minimum ADC and maximum FDOPA PET uptake in patients with newly diagnosed glioblastoma multiforme. MR imaging and FDOPA PET data were acquired preoperatively from 15 patients who were subsequently diagnosed with high-grade brain tumor (WHO grade III or IV) by histopathologic analysis. ADC and SUVR normalized FDOPA PET maps were registered to the corresponding CE MR imaging. Regions of minimum ADC within the FDOPA-defined tumor volume were anatomically correlated with areas of maximum FDOPA SUVR uptake. Minimal anatomic overlap was found between regions exhibiting minimum ADC (a putative marker of tumor cellularity) and maximum FDOPA SUVR uptake (a marker of tumor infiltration and proliferation). FDOPA SUVR measures for tumoral regions exhibiting minimum ADC (1.36±0.22) were significantly reduced compared with those with maximum FDOPA uptake (2.45±0.88, P=.0001). There was a poor correlation between minimum ADC and the most viable/aggressive component of high-grade gliomas. This study suggests that other factors, such as tissue compression and ischemia, may be contributing to restricted diffusion in GBM. Caution should be exercised in the clinical use of minimum ADC as a marker of tumor grade and the use of this index for guiding tumor biopsies preoperatively.

Highlights

  • BACKGROUND AND PURPOSEThere is significant interest in whether diffusion-weighted MR imaging indices, such as the minimum apparent diffusion coefficient, may be useful clinically for preoperative tumor grading and treatment planning

  • Minimal anatomic overlap was found between regions exhibiting minimum ADC and maximum FDOPA SUVR uptake

  • CE MR imaging only detects dysfunction of the blood-brain barrier, which, in many cases, may not correspond with tumor proliferation or other molecular events.[2]. Many of these limitations have been overcome by using PET molecular imaging technology with amino acid– based tumor cell tracers, such as methyl-11C-L-methionine[3] and 3,4-dihydroxy-6-[18F]fluoro-L-phenylalanine.[4,5]. Such tracers have been shown to be superior in the diagnostic assessment of patients with brain tumor compared with CE MR imaging and 2-deoxy-2-[18F]fluorodeoxyglucose PET.[4,6]

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Summary

Objectives

Because the aim of this study was to investigate the anatomic relationship between areas of minimum ADC with areas of high FDOPA uptake, reducing this threshold would impact the interpretation of the findings because larger minimum ADC volumes would most likely contain tissue with varying degrees of tumor infiltration

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Conclusion

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