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Efficacy and safety of different thermal ablative therapies for desmoid-type fibromatosis: a systematic review and meta-analysis
BACKGROUND: Desmoid-type fibromatosis (DF) is a locally aggressive tumor characterized by peripheral infiltration of neoplastic cells and remote metastasis disability. This systematic review examined the efficacy and safety of thermal ablative therapy for DF tumors. METHODS: A literature search was...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10585570/ https://www.ncbi.nlm.nih.gov/pubmed/37869315 http://dx.doi.org/10.21037/qims-23-289 |
Sumario: | BACKGROUND: Desmoid-type fibromatosis (DF) is a locally aggressive tumor characterized by peripheral infiltration of neoplastic cells and remote metastasis disability. This systematic review examined the efficacy and safety of thermal ablative therapy for DF tumors. METHODS: A literature search was conducted using PubMed, Web of Science, Cochrane Library, and Embase from January 1, 2000, to November 12, 2022. The Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement was used to guide literature selection. The inclusion criteria were the following: (I) the patients were diagnosed with aggressive fibromatosis pathologically, (II) the patients were treated by thermal ablations, and (III) a focus on treatment efficacy and safety. Meanwhile, the exclusion criteria were the following: (I) cohorts of patients with hypertrophic scar, Gardner fibroma, or nodular fasciitis; (II) conference abstracts, reviews, case reports, letters to editors, comments, or editorials; (III) number of patients <5; (IV) in vitro or animal experiments; and (V) non-English language articles. The inverse variance method with a random effects model was used to obtain the pooled data. Subgroup analyses were performed to identify treatment factors. Egger test was conducted to assess the risk of publication bias. RESULTS: After literature selection, 694 DF tumors were identified in 23 studies. In terms of modality, 13 studies used cryoablation, 9 studies used high-intensity focused ultrasound (HIFU), and 1 study used microwave ablation (MWA). The pooled symptom relief rate was 90% [95% confidence interval (CI): 80–97%], with that for HIFU being 100% (95% CI: 85–100%), that for cryoablation being 87% (95% CI: 74–97%), and that MWA being 89% (95% CI). The pooled major complication rate was 3% (95% CI: 1–7%), and that for each modality was as follows: HIFU =2% (95% CI: 0–6%), cryoablation =4% (95% CI: 1–8%), MWA =11%, ultrasound =6% (95% CI: 1–13%), computed tomography (CT) =2% (95% CI: 0–7%), and magnetic resonance imaging (MRI) =3% (95% CI: 0–14%). The pooled nonperfused volume rate (NPVR) was 76% (95% CI: 71–81%), and that for each modality was as follows: HIFU =77% (95% CI: 71–85%), cryoablation =74% (95% CI: 69–79%), ultrasound =75% (95% CI: 67–83%), CT =76% (95% CI: 67–87%), and MRI =78% (95% CI: 70–87%). The pooled local control rate was 88% (95% CI: 79–94%) and that for each modality was as follows: HIFU =99% (95% CI: 96–100%), cryoablation =80% (95% CI: 68–90%), and MWA =78%. The differences in major complication rate (P=0.77) and NPVR between imaging-guided modalities (P=0.40) were not significant, nor were the differences in symptom relief rate (P=0.32) and major complication rate (P=0.61) between ablative techniques; however, the differences in local control rate (P=0.01) were significant between ablative techniques. CONCLUSIONS: Imaging-guided thermal ablative therapies contribute to symptom relief with a duration of more than 6 months and a low major complication rate of DF tumors. |
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