Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2016 Jun;18(6):873-80.
doi: 10.1093/neuonc/nov301. Epub 2015 Dec 19.

A prospective trial of dynamic contrast-enhanced MRI perfusion and fluorine-18 FDG PET-CT in differentiating brain tumor progression from radiation injury after cranial irradiation

Affiliations

A prospective trial of dynamic contrast-enhanced MRI perfusion and fluorine-18 FDG PET-CT in differentiating brain tumor progression from radiation injury after cranial irradiation

Vaios Hatzoglou et al. Neuro Oncol. 2016 Jun.

Abstract

Background: The aim of this study was to assess the effectiveness of fluorine-18 fluorodeoxyglucose (FDG) PET-CT and dynamic contrast-enhanced (DCE) MRI in differentiating tumor progression and radiation injury in patients with indeterminate enhancing lesions after radiation therapy (RT) for brain malignancies.

Methods: Patients with indeterminate enhancing brain lesions on conventional MRI after RT underwent brain DCE-MRI and PET-CT in a prospective trial. Informed consent was obtained. Lesion outcomes were determined by histopathology and/or clinical and imaging follow-up. Metrics obtained included plasma volume (Vp) and volume transfer coefficient (K(trans)) from DCE-MRI, and maximum standardized uptake value (SUVmax) from PET-CT; lesion-to-normal brain ratios of all metrics were calculated. The Wilcoxon rank sum test and receiver operating characteristic analysis were performed.

Results: The study included 53 patients (29 treated for 29 gliomas and 24 treated for 26 brain metastases). Progression was determined in 38/55 (69%) indeterminate lesions and radiation injury in 17 (31%). Vpratio (VP lesion/VP normal brain, P < .001), K(trans) ratio (P = .002), and SUVratio (P = .002) correlated significantly with diagnosis of progression versus radiation injury. Progressing lesions exhibited higher values of all 3 metrics compared with radiation injury. Vpratio had the highest accuracy in determining progression (area under the curve = 0.87), with 92% sensitivity and 77% specificity using the optimal, retrospectively determined threshold of 2.1. When Vpratio was combined with K(trans) ratio (optimal threshold 3.6), accuracy increased to 94%.

Conclusions: Vpratio was the most effective metric for distinguishing progression from radiation injury. Adding K(trans) ratio to Vpratio further improved accuracy. DCE-MRI is an effective imaging technique for evaluating nonspecific enhancing intracranial lesions after RT.

Keywords: 18F-FDG PET-CT; DCE MRI perfusion; radiation injury.

PubMed Disclaimer

Figures

Fig. 1.
Fig. 1.
Receiver operating characteristic (ROC) analysis for Vpratio, Ktransratio, and SUVratio demonstrating the optimal cutoffs to be 2.1, 3.6, and 1.2, respectively, in distinguishing between progression and radiation injury.
Fig. 2.
Fig. 2.
Patient example of tumor progression detected by DCE-MRI perfusion. Images obtained in a 30-year-old man with metastatic sarcoma who underwent SRS to a left parietal lobe metastasis. Axial contrast-enhanced T1-weighted image before treatment (A) shows an enhancing mass (arrow) that increases in size 6 months after treatment (B). Vp map of the enlarging mass (C) demonstrates increased perfusion; however, PET-CT showed no abnormal FDG uptake (D). Pathology confirmed progression.
Fig. 3.
Fig. 3.
Patient example of radiation injury detected by DCE-MRI perfusion and PET-CT. Images obtained in a 39-year-old woman with metastatic breast cancer who underwent SRS to a left frontal lobe metastasis. Axial contrast-enhanced T1-weighted image (A) demonstrates an enhancing mass that had increased in size 1 year after SRS (arrow). DCE-MRI showed no increase in perfusion on the Vp map (B) and no increase in SUV on PET-CT (C). The lesion remained stable 1 year after it had enlarged (D) without any additional therapy and was determined to represent radiation injury.

Comment in

References

    1. Stupp R, Mason WP, van den Bent MJ et al. Radiotherapy plus concomitant and adjuvant temozolomide for glioblastoma. N Engl J Med. 2005;352(10):987–996. - PubMed
    1. Stupp R, Hegi ME, Mason WP et al. Effects of radiotherapy with concomitant and adjuvant temozolomide versus radiotherapy alone on survival in glioblastoma in a randomised phase III study: 5-year analysis of the EORTC-NCIC trial. Lancet Oncol. 2009;10(5):459–466. - PubMed
    1. Patchell RA, Tibbs PA, Regine WF et al. Postoperative radiotherapy in the treatment of single metastases to the brain: a randomized trial. JAMA. 1998;280(17):1485–1489. - PubMed
    1. Kocher M, Soffietti R, Abacioglu U et al. Adjuvant whole-brain radiotherapy versus observation after radiosurgery or surgical resection of one to three cerebral metastases: results of the EORTC 22952-26001 study. J Clin Oncol. 2011;29(2):134–141. - PMC - PubMed
    1. Dropcho EJ. Neurotoxicity of radiation therapy. Neurol Clin. 2010;28(1):217–234. - PubMed

Publication types

Substances