Percutaneous cryoablation for the treatment of extra-abdominal desmoid tumors
Kaila Redifer Tremblay, William B Lea, John C Neilson, David M King, Sean M Tutton, Kaila Redifer Tremblay, William B Lea, John C Neilson, David M King, Sean M Tutton
Abstract
Background: Desmoid tumors are rare locally invasive, benign neoplasms that develop along aponeurotic structures. Current treatment is complicated by associated morbidity and high recurrence rates.
Methods: A retrospective, single-institution review identified 23 patients (age: 16-77) with extra-abdominal desmoid tumors who received CT-guided percutaneous cryoablation as either a first-line (61%) or salvage (39%) treatment in 30 sessions between 2014 and 2018. Median maximal lesion diameter was 69 mm (range: 11-209). Intent was curative in 52% and palliative in 48%. Contrast-enhanced cross-sectional imaging was obtained before and after treatment in addition to routine clinical follow-up.
Results: Technical success was achieved in all patients. The median follow-up was 15.4 months (3.5-43.4). Symptomatic improvement was demonstrated in 89% of patients. At 12 months, the average change in viable volume was -80% (range -100% to + 10%) and response by modified response evaluation criteria in solid tumors (mRECIST) was CR 36%, PR 36%, and SD 28% No rapid postablation growth or track seeding was observed. Four patients underwent repeat cryoablation for either residual or recurrent disease. Two patients sustained a major procedural complication consisting of significant neuropraxia.
Conclusion: Cryoablation for desmoid tumors demonstrates a high degree of symptom improvement and local tumor control on early follow-up imaging with relatively low morbidity.
Keywords: ablation; aggressive fibromatosis; cryoablation; desmoid; sarcoma.
© 2019 Wiley Periodicals, Inc.
Figures
References
- Nieuwenhuis MH, Casparie M, Mathus‐Vliegen LMH, Dekkers OM, Hogendoorn PC, Vasen HF. A nation‐wide study comparing sporadic and familial adenomatous polyposis‐related desmoid‐type fibromatoses. Int J Cancer. 2011;129:256‐261. 10.1002/ijc.25664
- Molloy AP, Hutchinson B, O'toole GC. Extra‐abdominal desmoid tumours: a review of the literature. Sarcoma. 2012;2012:1‐9. 10.1155/2012/578052.
- Eastley N, McCulloch T, Esler C, et al.Extra‐abdominal desmoid fibromatosis: a review of management, current guidance and unanswered questions. Eur J Surg Oncol. 2016;42:1071‐1083. 10.1016/j.ejso.2016.02.012
- Salas S, Dufresne A, Bui B, et al. Prognostic factors influencing progression‐free survival determined from a series of sporadic desmoid tumors: A wait‐and‐see policy according to tumor presentation. J Clin Oncol. 2011;29:3553‐3558. 10.1200/JCO.2010.33.5489
- Bonvalot S, Ternès N, Fiore M, et al. Spontaneous regression of primary abdominal wall desmoid tumors: More common than previously thought. Ann Surg Oncol. 2013;20:4096‐4102. 10.1245/s10434-013-3197-x
- 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;51:186‐192. 10.1016/j.ejca.2014.11.019
- Crago AM, Denton B, Salas S, et al. A prognostic nomogram for prediction of recurrence in desmoid fibromatosis. Ann Surg. 2013;258:347‐353. 10.1097/SLA.0b013e31828c8a30
- Kurup AN, Callstrom MR. Expanding role of percutaneous ablative and consolidative treatments for musculoskeletal tumours. Clin Radiol. 2017;72:645‐656. 10.1016/j.crad.2017.02.019
- Cazzato RL, Garnon J, Ramamurthy N, et al. Percutaneous image‐guided cryoablation: current applications and results in the oncologic field. Med Oncol. 2016;33:140 10.1007/s12032-016-0848-3
- von Mehren M, Randall RL, Benjamin RS, et al. Soft tissue sarcoma, Version 2.2018, NCCN Clinical Practice Guidelines in Oncology. J Natl Compr Canc Netw. 2018;16:536‐563. 10.6004/jnccn.2018.0025
- Schmitz JJ, Schmit GD, Atwell TD, et al. Percutaneous cryoablation of extraabdominal desmoid tumors: a 10‐year experience. Am J Roentgenol. 2016;207:190‐195. 10.2214/AJR.15.14391
- 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;37:1500‐1506. 10.1007/s00270-013-0830-9
- Harris PA, Taylor R, Thielke R, et al. Research electronic data capture (REDCap)–A metadata‐driven methodology and workflow process for providing translational research informatics support. J Biomed Inform. 2009;42:377‐381.
- 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. J Vasc Interv Radiol. 2017;28:1432‐1437. 10.1016/j.jvir.2017.06.019
- Littrup PJ, Ahmed A, Aoun HD, et al. CT‐guided percutaneous cryotherapy of renal masses. J Vasc Interv Radiol. 2007;18:383‐392. 10.1016/j.jvir.2006.12.007
- Lev D, Kotilingam D, Wei C, et al. Optimizing treatment of desmoid tumors. J Clin Oncol. 2007;25:1785‐1791. 10.1200/JCO.2006.10.5015
- Nuyttens JJ, Rust PF, Thomas CR, Turrisi AT. Surgery versus radiation therapy for patients with aggressive fibromatosis or desmoid tumors: a comparative review of 22 articles. Cancer. 2000;88:1517‐1523. 10.1002/(SICI)1097-0142(20000401)88:7<1517::AID-CNCR3>;2-9
- Keus RB, Nout RA, Blay J‐Y, et al. Results of a phase II pilot study of moderate dose radiotherapy for inoperable desmoid‐type fibromatosis—an EORTC STBSG and ROG study (EORTC 62991‐22998). Ann Oncol. 2013;24:2672‐2676. 10.1093/annonc/mdt254
- Hansmann A, Adolph C, Vogel T, et al. High‐dose tamoxifen and sulindac as first‐line treatment for desmoid tumors. Cancer. 2004;100:612‐620. 10.1002/cncr.11937
- Fiore M, Colombo C, Radaelli S, et al. Hormonal manipulation with toremifene in sporadic desmoid‐type fibromatosis. Eur J Cancer. 2015;51:2800‐2807. 10.1016/j.ejca.2015.08.026
- Penel N, Le Cesne A, Bonvalot S, et al. Surgical versus non‐surgical approach in primary desmoid‐type fibromatosis patients: a nationwide prospective cohort from the French Sarcoma Group. Eur J Cancer. 2017;83:125‐131. 10.1016/j.ejca.2017.06.017
- Kasper B, Gruenwald V, Reichardt P, et al. Imatinib induces sustained progression arrest in RECIST progressive desmoid tumours: Final results of a phase II study of the German Interdisciplinary Sarcoma Group (GISG). Eur J Cancer. 2017;76:60‐67. 10.1016/j.ejca.2017.02.001
- Bishop AJ, Zarzour MA, Ratan R, et al. Long‐term outcomes for patients with desmoid fibromatosis treated with radiation therapy: a 10‐year update and re‐evaluation of the role of radiation therapy for younger patients. Int J Radiat Oncol. 2019;103:1167‐1174. 10.1016/j.ijrobp.2018.12.012
- Gangi A Evaluation of the cryodestruction of non abdominopelvic desmoid tumors in patients progressing despite medical treatment‐tabular view‐. . 2018. (accessed August 14, 2018).
Source: PubMed