Nienke S. de Jager1, Tim J. van Oostenbrugge2, Torben Pätz3, Sjoerd F.M. Jenniskens1, Jurgen J. Fütterer1, Hans Langenhuijsen2, and Christiaan G. Overduin1
1Medical Imaging, Radboudumc, Nijmegen, Netherlands, 2Urology, Radboudumc, Nijmegen, Netherlands, 3Fraunhofer Institute for Digital Medicine, Bremen, Germany
Synopsis
MRI-guided cryoablation of small renal tumors relies
on achieving sufficient ice ball coverage throughout the entire lesion for
effective treatment. However, a volumetric approach to assess treatment margins
intraoperatively is currently lacking. This work retrospectively derived
three-dimensional ablation margins after cryoablation in 39 kidney tumors using
co-registration of intraoperatively acquired pre- and post-ablation MR images.
Minimal ablation margins were significantly smaller for cases with versus
without local tumor progression. Radiological complete coverage (ablation
margin >0 mm) was associated with local control. MRI-derived 3D ablation
margins may present a useful intraprocedural tool to assess treatment success.
Introduction
Percutaneous
cryoablation is an accepted treatment alternative in patients with small renal
tumors1. MRI-guidance allows several advantages over standard
computer tomography (CT)-guidance, including the capability of high soft-tissue
contrast without contrast medium, multiplanar imaging and near real-time
monitoring of volumetric ice ball progression2. The capability to
visualize the entire ice ball volume enables image-based assessment of volumetric
tumor coverage but a validated intraoperative approach is currently lacking. In
practice, most interventionalists aim for a treatment margin of 5 mm to
minimize the risk for local recurrent disease3. Recent studies
however have suggested renal tumors may be effectively treated at smaller
treatment margins of 1-1.5 mm4-5, but were limited to
two-dimensional measurements or CT-based delineations. Therefore, the purpose of this work was to retrospectively assess three-dimensional
(3D) minimal ablation margins after MRI-guided percutaneous cryoablation of
small renal tumors using intraoperative MR-MR image co-registration and
determine its correlation with local treatment success.Methods
Between
May 2014 and January 2021, 34 patients (mean age: 69y) underwent percutaneous
MRI-guided cryoablation at our institution for 39 small renal tumors (size:
1.6-5.1 cm) and were at least 6 months after treatment. All procedures were
performed under general anesthesia on a 3-T clinical MR system (Magnetom Skyra,
Siemens). Intraprocedural pre-ablation imaging consisted of bi-plane
T2-weighted half fourier spin echo (HASTE) imaging in apnea when possible. Needle
insertion was performed under ultrasound guidance at a safe zone within the
MRI-suite or in case of poor visibility on ultrasound under direct MR imaging
guidance. After confirmation of probe placement with MRI, cryoablation was
performed in two 10:3 minute freeze-thaw cycles. Continuous monitoring of ice
ball progression was performed using biplanar T2 HASTE or T1-weighted stack of
stars volume interpolated gradient echo (STARVIBE) acquisitions, where the
final acquisition was performed at the end of ablation when possible in apnea. After
the procedures, tumor and ice-ball volumes were semi-automatically segmented on
the intraprocedural pre- and corresponding end-of-ablation MR images using
Software Assistant for Interventional Radiology (SAFIR) research software
(Fraunhofer, Germany). Using the same software, pre- and post-ablation MR
images were aligned using manual landmark-based rigid co-registration, after
which volumetric ablation margins were automatically quantified (Figure 1).
The minimal ablation margin (MAM) was defined as the smallest 3D distance
between the tumor and ice-ball surface. Local tumor progression (LTP) after
cryoablation was assessed on follow-up imaging.Results
Median
follow-up was 20 months (range: 1-58). Local control after cryoablation was
achieved in 33 tumors (85%) while LTP occurred in 6 (15%). Retrospective
analysis of the 3D ablation margin using intraoperative pre- and post-ablation MR
image co-registration was feasible in all patients (100%) (Figure 2). Minimal
ablation margin was significantly smaller for cases with (-6.9±3.5 mm) vs.
without LTP (2.3±1.9 mm) (P<.001) (Figure 3). No LTP was observed in
patients with a MAM ≥0 mm. Cases with LTP had significantly larger tumor diameters
(4.1±0.5 vs. 2.9±0.8 cm, P<.001). All negative treatment margins occurred in
patients with tumor size >3 cm (Figure 4).Discussion
Two
recent studies have indicated a MAM of 1-1.5 mm to be sufficient for effective
renal cryoablation4-5. Although a safety margin remains preferable,
our preliminary clinical data indicates a MAM ≥0 mm to be predictive of local
tumor control. In part, these findings may be due to the ability to assess the
treatment margin in 3D, which may in some areas be smaller than the recommended
5 mm without leading to local tumor recurrence. In addition, cryoablation is
known to cause direct thermal damage as well as delayed cytotoxic effects,
mainly due to thrombosis causing local ischemia6. These effects may
not yet be captured on the intraprocedural MRI visualizing the total ice
extent, and possibly contribute to a smaller intraprocedurally determined
treatment margin to be sufficient for complete ablation. Contrary to previous
studies that have used contrast-enhanced CT or 1-day post-treatment MRI, the
present method relies on non-contrast intraoperative MRI and therefore shows
potential for intraprocedural use. Main limitations of the current work are its
limited sample size, single observer and potential inaccuracies arising from
the annotation and co-registration process that require further validation in
larger cohorts.Conclusion
Volumetric
assessment of the periablational treatment margin using intraoperative MR-MR
image fusion was feasible and can be useful as an intraprocedural tool to
evaluate local treatment success of MR-guided cryoablation for small renal
tumors. Ablations with incomplete radiological coverage (ablation margin <0
mm) were associated with local tumor progression.Acknowledgements
No acknowledgement found.References
1. Ljungberg et al. Eur Urol. 2019;75(5):799-810.
2. Mogami et al. Int J Clin Oncol. 2007;12(2):79-84
3. Ahmed et al. Radiology 2014;273(1):241–260
4. Ge et al. J Vasc Interv Radiol. 2016;27(3):403-9.
5. Fraisse et al. BJU Int. 2019;123(4):632-8.
6. Erinjeri et al. J Vasc Interv Radiol. 2010;21(8 Suppl):S187-91