Copenhagen, Denmark
Onsite/Online

ESTRO 2022

Session Item

Saturday
May 07
09:00 - 10:00
Poster Station 1
01: Image processing & analysis
René Winter, Norway
1180
Poster Discussion
Physics
3D MRI versus conventional ultrasound tumour measurements for treatment planning of eye tumours
Lisa Klaassen, The Netherlands
PD-0075

Abstract

3D MRI versus conventional ultrasound tumour measurements for treatment planning of eye tumours
Authors:

Lisa Klaassen1,2,3, Myriam Jaarsma-Coes2,1, Teresa Ferreira2, Khanh Vu1, Marina Marinkovic4, Gregorius Luyten1, Coen Rasch3, Jan-Willem Beenakker1,2,5

1Leiden University Medical Center, Ophthalmology, Leiden, The Netherlands; 2Leiden University Medical Center, Radiology, Leiden, The Netherlands; 3Leiden University Medical Center, Radiation Oncology, Leiden, The Netherlands; 4Leiden University Medical Center, Ophthalmology, Leide, The Netherlands; 5Leiden University Medical Center, Radiation Oncology, Leiden, The Netherlands

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Purpose or Objective

Uveal melanoma (UM) is the most frequently occurring malignant primary eye tumour. Ocular MRI, enabling 3D tumour imaging and providing a better soft tissue contrast than conventional 2D ultrasound (US), is increasingly used for the diagnosis, therapy planning and follow-up of UM. Tumour prominence (thickness) and largest basal diameter (LBD) are the primary determinants for the brachytherapy applicator size and application time and are used to define the 3D clinical target volume in proton beam therapy. Within this study, we aim to compare US and MRI dimension measurements and determine the most suitable measurement modality. 

Material and Methods

Data of 25 UM patients with a wide range in size and location were analysed retrospectively. Patients were scanned at 3 Tesla MRI according to the protocol of Ferreira (Cancers 2019). The tumour was semi-automatically delineated on the contrast-enhanced T1-weighted images (acquisition voxel size 0.8x0.8x0.8 mm3) in MevisLab.

The prominence and LBD were automatically obtained from the MRI contours. MRI measurements were compared to the clinical US measurements (resolution 0.4 mm) and related to tumour location in the anteroposterior direction. Tumours where the measurement did not fit into the US field of view (FOV) or where the extent of flat tumour components was difficult to assess on MRI were assessed separately.

Results

For 7/25 patients, the prominence and/or LBD measurement did not fit into the US FOV. All these tumours were located in the anterior 50% of the eye. Of the 4 patients with an US prominence <4 mm, tumour extent was difficult to assess on MRI for 3/4 (Fig 1).

When tumour extent was visible on both imaging modalities, median absolute differences were 0.3 mm (range 0.0-1.3 mm) for prominence and 1.1 mm (range 0.1-2.8 mm) for LBD, respectively (Fig 2). For the LBD, 80% of measurements was more than 0.5 mm larger on MRI. For patients for whom the tumour extent was difficult to assess on one imaging modality, the median absolute difference for the prominence and LBD were 0.7 mm (range 0.5-1.6 mm) and 1.4 mm (range 0.1-7.6 mm).

 

Conclusion

MRI and US yield similar prominence measurements (median absolute difference 0.3 mm) when tumour extent is visible on both modalities. However, in anteriorly located tumours, MRI measurements are more accurate, and using US for these tumours might lead to an underestimation of tumour diameter, possibly due to difficulty correctly positioning the ultrasound transducer. The extent of flat tumours can be difficult to assess on MRI, although, the distinction between tumour and healthy tissue may not be evident on US either. For these tumours, tumour measurements may be supported by fundoscopic imaging.