Safety and efficacy of cryoablation of soft-tissue tumours: a systematic review

Author:

Bodard Sylvain1234ORCID,Marcelin Clement5,Kastler Adrian6,Dimopoulos Platon M17,Petre Elena N1,Frandon Julien8,Razakamanantsoa Leo9,Cornelis Francois H129ORCID

Affiliation:

1. Department of Radiology, Memorial Sloan Kettering Cancer Center , New York, NY 10065, USA

2. Department of Radiology, Weill Cornell Medical College , New York, NY 10065, USA

3. Department of Radiology, Necker Hospital, University of Paris Cité , Paris 75015, France

4. CNRS UMR 7371, INSERM U 1146, Laboratoire d’Imagerie Biomédicale, Sorbonne University , Paris 75006, France

5. Department of Radiology, Centre Hospitalo-Universitaire de Bordeaux , Bordeaux 33076, France

6. Neuroradiology and MRI Unit, Grenoble Alpes University Hospital , Grenoble Cedex 09, France

7. Interventional Radiology Department, University Hospital of Patras , Patras 26504, Greece

8. Radiology Department, Nimes University Hospital , Nimes 30900, France

9. Department of Interventional Radiology and Oncology, Tenon Hospital, Sorbonne University , Paris 75020, France

Abstract

Abstract Objectives To assess the safety and efficacy of percutaneous cryoablation (CA) of soft-tissue tumours [desmoid tumours (DTs), vascular malformations (VMs), and abdominal wall endometriosis (AWE)]. Methods This systematic review of studies published before January 2024 encompassed a detailed analysis of CA techniques and technical aspects for the treatment of soft-tissue tumours. Data concerning CA efficacy, complication rates, and other relevant metrics were extracted and included for analysis. Results The analysis included 27 studies totalling 554 CA procedures. For DT (13 studies, 393 sessions), CA showed an average pain reduction of 79 ± 17% (range: 57-100) and a lesion volume decrease of 71.5 ± 9.8% (range: 44-97). VM (4 studies, 58 sessions) had a 100% technical success rate and an average pain reduction of 72 ± 25% (range: 63-85). The average pain reduction for AWE (6 studies, 103 sessions) was 82 ± 13% (range: 62-100). Overall, the complication rate for CA was low, with minor adverse events (AEs) in about 20% of patients and major events in less than 5% of patients. Conclusions Showing substantial efficacy in pain reduction and lesion volume decrease, as well as low incidence of severe AE, CA presents as a highly effective and safe alternative for the treatment of soft-tissue tumours. Advances in knowledge CA is effective and safe in treating soft-tissue tumours, particularly DT, VM, and AWE.

Funder

NIH

NCI Cancer Center

Publisher

Oxford University Press (OUP)

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