Ali Agely1, Vipul Sheth1, Pejman Ghanouni1, and Ryan L. Brunsing1
1Radiology, Stanford University, Palo Alto, CA, United States
Synopsis
Desmoid tumors are
challenging to control with chemotherapy, surgery, or radiation. This
retrospective review evaluated patients with extra-abdominal desmoid tumors treated
with MR-guided cryoablation at our institution over two years. The primary
endpoint was tumor volume change before and 3 months after cryoablation; the
secondary endpoint was the change in health status assessed at the same
interval. Our study demonstrates MR-guided cryoablation results in the reduction
of both tumor size and improvement in health status scores. No severe adverse
events occurred. We conclude that MR-guided cryoablation is an effective and
safe treatment option for desmoid tumors.
Introduction
Desmoid
tumors are rare monoclonal tumors consisting of spindle fibrocyte-like cells
that form along the musculoaponeurotic structures1. These tumors lack metastatic
potential but can cause significant morbidity from local infiltration around
nerves, vessels, and muscles. Current treatment strategies include observation2-4, surgical resection, radiation,
systemic therapy, high intensity focused ultrasound5,6, and percutaneous thermal ablation
(radiofrequency ablation and cryoablation)7-10. While initially used primarily in
the salvage setting, the 2020 treatment guidelines from the National
Comprehensive Cancer Network (NCCN) lists ablation as a first-line therapeutic option
for extra-abdominal desmoid tumors11.
This
study investigates our initial two-year experience with MR-guided cryoablation treatment
of extra-abdominal desmoid tumors.Methods
Patient
Selection
After
approval from our institutional review board, we retrospectively reviewed patients
with biopsy-proven desmoid tumors treated with MRI-guided percutaneous
cryoablation between 2019-2020 (Figure 1). All patients underwent multi-disciplinary
evaluation. Patients had pre-procedure and 3-month post-treatment MR imaging.
Data
Collection
Data
recorded through a retrospective chart review included demographic patient
information, prior treatments, symptoms, lesion volume, therapy specifications,
and complications.
Pre-ablation
and three-month
post-ablation assessment compared 1) pre- and post-ablation viable tumor volume
measured by contouring the tumor on subtracted post-contrast MRI, and 2)
changes in health status based on the 36-item short-form questionnaire (SF-36)12. Complications were recorded per the
Society of Interventional Radiology Adverse Event Severity Scale13.
Cryoablation
Technique
After
informed consent, general anesthesia was induced. Angiocatheters (14g Becton
Dickinson) were advanced into the tumor under ultrasound- and MRI-guidance for
tumor penetration. Placement of cryoprobes (Visual ICE Cryoablation System,
Boston Scientific, USA) at the appropriate depth through angiocatheters were confirmed with MRI. The radiologist determined the number of probes based on
the targeted tumor size (median: 6; range: 2 – 16). Hydro-dissection was
performed under ultrasound- and MRI-guidance to ensure the safety of the
adjacent structures. Measures for skin protection included warming packs, warmed
ultrasound gel, and warmed saline.
The number (median: 4 cycles; range 2 – 6 cycles)
and duration (median: 8 minutes, range 3.5 – 15 minutes) of
freeze-thaw cycles varied based on tumor size and proximity to critical
structures. The goal was to extend the ice ball 5 mm beyond the tumor margin while
avoiding critical structures. During all cryoablation cycles, ice ball proximity
to critical structures was monitored with intermittent MR imaging (Figure 2). Patients
were discharged or admitted for observation depending on the complexity
of the procedure and medical comorbidities. Complications were assessed
immediately after, 1-day, 2-days, 1-week, and 3-months following the procedure.
Post-cryoablation
MRI was performed at the 3-month interval.Results
A
total of 16 patients (median age: 40, range 17 – 83; 10 females) received
18 MR-guided percutaneous cryoablation procedures (Table 1). Two patients
required repeat procedures due to tumor size. Lesions were in the extremities, shoulder,
chest wall, pelvis, back, and breast. The median pretreatment tumor volume was 56
cm3 (mean: 119 cm3, range: 2 – 600 cm3) (Table 2).
In seven patients, complete ablation
was the pre-treatment goal. The mean residual tumor volume was 5.2% at follow
up (range
0 – 19.8%). Two adverse events occurred in this
subgroup: a small pneumothorax, which required no intervention, and contact
dermatitis, possibly from adhesive tape. All patients had improved health
status scores following cryoablation (Table 3).
Subtotal
cryoablation was performed in nine patients due to the
proximity to critical structures, with the intent to control tumor size and
symptoms. The mean
residual tumor volume was 42.9% at follow-up (range 15.9-78.2%). Fragmentation of the angiocatheter
tip occurred in two patients while one patient had a post-procedure pulmonary
embolism. Changes in health status scores were
relatively small and inconsistent (Table 3). Discussion
Our
study demonstrates the safety and efficacy of MR guided cryoablation of desmoid
tumors. At three-month follow-up, all patients had reduced viable tumor volumes,
including three patients with no residual tumor. Although endpoints vary and our follow-up is shorter, our outcomes are encouraging when compared
with medical approaches to management, which have reported measurable response
rates (decreased tumor diameter) of 31%14 and 33%15 at 12 months or lack of progression
rates at 6 months between 45 – 83.7%16. Patients with the intention of
complete ablation reported improved health status scores on all components of the
SF-36 questionnaire. Patients treated with the intention of
tumor control reported little change in health status; it is possible for some patients that the same proximity to nerves that limited total ablation
allowed for ongoing symptoms despite the reduction in overall tumor volume.
Our
mean decrease in viable tumor volume of 73.6% at 3 months is similar to prior studies. Redifer
Tremblay et al reported a mean 81% decrease in viable tumor volume at 16.8
months in 23 desmoid patients who underwent cryoablation; tumor size (mean:114.8 cm, range: 0.4 – 456.5 cm3) was similar to our cohort10. Schmitz et al reported a mean 70%
decrease in viable tumor volume in 18 patients with a mean tumor size of 38.1 cm3
(1.6 – 118.3 cm3)9, while Havez et al reported a mean
87% decrease in viable tumor volume in 13 patients8.
Limitations of the study include small sample
size, single-institution experience, and short follow-up. Conclusion
MR-guided
cryoablation is a safe and efficacious treatment strategy for extra-abdominal
desmoid tumors.Acknowledgements
No acknowledgement found.References
1.
Alman BA, Pajerski ME, Diaz-Cano S, Wolfe HJ. Aggressive fibromatosis (desmoid
tumor) is A. Diagn Mol Pathol. 1997;6(2):98-101.
2.
Bonvalot S, Ternès N, Fiore M, et al. Spontaneous regression of primary
abdominal wall desmoid tumors: More common than previously thought. Annals
of Surgical Oncology. 2013;20(13):4096-4102.
3.
Eastley N, McCulloch T, Esler C, et al. Extra-abdominal desmoid fibromatosis: A
review of management, current guidance and unanswered questions. European
Journal of Surgical Oncology (EJSO). 2016;42(7):1071-1083.
4.
Colombo C, Miceli R, Le Péchoux C, et al. Sporadic extra abdominal wall
desmoid-type fibromatosis: Surgical resection can be safely limited to a
minority of patients. Eur J Cancer. 2015;51(2):186-192.
5.
Ghanouni P, Dobrotwir A, Bazzocchi A, et al. Magnetic resonance-guided focused
ultrasound treatment of extra-abdominal desmoid tumors: A retrospective
multicenter study. Eur Radiol. 2017;27(2):732-740.
6.
Wang Y, Wang W, Tang J. Ultrasound-guided high intensity focused ultrasound
treatment for extra-abdominal desmoid tumours: Preliminary results. International
Journal of Hyperthermia. 2011;27(7):648-653.
7.
Kurtz J, Buy X, Deschamps F, et al. CRYODESMO-O1: A prospective, open phase II
study of cryoablation in desmoid tumour patients progressing after medical
treatment. Eur J Cancer. 2020;143:78-87.
8.
Havez M, Lippa N, Al-Ammari S, et al. Percutaneous image-guided cryoablation in
inoperable extra-abdominal desmoid tumors: A study of tolerability and
efficacy. Cardiovasc Intervent Radiol. 2014;37(6):1500-1506.
9.
Schmitz JJ, Schmit GD, Atwell TD, et al. Percutaneous cryoablation of
extraabdominal desmoid tumors: A 10-year experience. Am J Roentgenol.
2016;207(1):190-195.
10.
Redifer Tremblay K, Lea WB, Neilson JC, King DM, Tutton SM. Percutaneous
cryoablation for the treatment of extra‐abdominal desmoid tumors. J Surg
Oncol. 2019;120(3):366-375.
11.
National Comprehensive Cancer Network. Clinical practice guidelines in oncology
(NCCN guidelines) soft tissue sarcoma version 2. 2019. Im Internet: www.nccn.org. 2020.
12.
Ware Jr JE. SF-36 health survey update. Spine. 2000;25(24):3130-3139.
13.
Khalilzadeh O, Baerlocher MO, Shyn PB, et al. Proposal of a new adverse event
classification by the society of interventional radiology standards of practice
committee. Journal of Vascular and Interventional Radiology. 2017;28(10):1432-1437.
e3.
14.
Skapek SX, Ferguson WS, Granowetter L, et al. Vinblastine and methotrexate for
desmoid fibromatosis in children: Results of a pediatric oncology group phase
II trial. Journal of Clinical Oncology. 2007;25(5):501-506.
15.
Gounder MM, Mahoney MR, Van Tine BA, et al. Sorafenib for advanced and
refractory desmoid tumors. N Engl J Med. 2018;379(25):2417-2428.
16.
Toulmonde M, Pulido M, Ray-Coquard I, et al. Pazopanib or
methotrexate–vinblastine combination chemotherapy in adult patients with
progressive desmoid tumours (DESMOPAZ): A non-comparative, randomised,
open-label, multicentre, phase 2 study. The Lancet Oncology.
2019;20(9):1263-1272.