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腹壁硬纤维瘤的外科治疗:系统评价和荟萃分析。

Surgical management of abdominal desmoids: a systematic review and meta-analysis.

机构信息

Department Surgery, Tallaght University Hospital, Tallaght, Dublin, D24 NR04, Ireland.

Royal College of Surgeons in Ireland, 123 St Stephens Green, Dublin 2, Ireland.

出版信息

Ir J Med Sci. 2023 Apr;192(2):549-560. doi: 10.1007/s11845-022-03008-8. Epub 2022 Apr 21.

Abstract

BACKGROUND

Desmoid tumours are benign fibromatous tumours arising from dysregulated myofibroblast proliferation within musculoaponeurotic structures. They can occur sporadically but more commonly are associated with genetic syndromes such as familial adenomatous polyposis (Sakorafas et al. in Surg Oncol 16(2):131-142, 2007) (FAP). Mutations in either the Wnt, β-catenin or APC genes are 'key' triggers for the development of these tumours (Howard and Pollock in Oncol Ther 4(1):57-72, 2016). Classically, these tumours do not metastasise; however, they are associated with significant morbidity and mortality due to their infiltrative pattern and/or local invasion. Historically, surgical resection was the cornerstone of treatment. There remains paucity of data regarding outcomes following the surgical management of abdominal desmoid tumours in terms of success, recurrence and morbidity.

OBJECTIVES

The aim of this review was to assess the current evidence for surgical management of abdominal desmoid tumours in terms of success, recurrence and morbidity.

METHODS

A systematic search of articles in PubMed, EMBASE and The Cochrane Library databases was performed according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines for the period from January 2000 to November 2020.

RESULTS

Twenty-three studies were included, of which, 749 patients had surgical resection (696 for primary and 53 for recurrent desmoids), 243 patients (18.8%) were medically managed and 353 patients (27.3%) underwent surveillance. Median follow-up was 51.4 months (range 1-372). Six-hundred and ninety-six of the 749 resections (92.9%) underwent primary desmoid resection, with the remaining 53 (7.1%) undergoing resection for recurrence. One-hundred and two surgically managed patients (19%) developed a (re)recurrence, with mesenteric involvement the commonest site for recurrence (55%). When comparing recurrence post-surgery to progression following medical therapy, there was a trend towards better outcomes with surgery, with 25% of surgical patients having a recurrence versus 50.5% having progression with medical therapy [OR 0.40 (95% CI 0.06-2.70), p = 0.35]. Major morbidity following surgery was 4.4% (n = 33) with 2% (n = 14) mortality within 30 days of resection.

CONCLUSION

The management of desmoids has considerable heterogeneity. Surgical resection for abdominal desmoids remains a valid treatment option in highly selective cases where negative margins can be obtained, with low major morbidity and/or mortality.

摘要

背景

纤维瘤病是一种良性纤维母细胞瘤,起源于肌纤维母细胞增殖失调,发生于肌肉腱膜结构。它们可以偶然发生,但更常见于与遗传综合征有关,如家族性腺瘤性息肉病(Sakorafas 等人,Surg Oncol 16(2):131-142, 2007)(FAP)。Wnt、β-catenin 或 APC 基因的突变是这些肿瘤发展的“关键”触发因素(Howard 和 Pollock,Oncol Ther 4(1):57-72, 2016)。经典上,这些肿瘤不会转移;然而,由于其浸润性模式和/或局部侵袭,它们与显著的发病率和死亡率相关。历史上,手术切除是治疗的基石。目前关于腹部纤维瘤病手术治疗的成功、复发和发病率的数据仍然很少。

目的

本综述的目的是评估目前在腹部纤维瘤病的手术治疗方面,在成功率、复发率和发病率方面的证据。

方法

根据系统评价和荟萃分析的首选报告项目的指南,对 PubMed、EMBASE 和 The Cochrane Library 数据库中的文章进行了系统搜索,检索时间为 2000 年 1 月至 2020 年 11 月。

结果

纳入了 23 项研究,其中 749 例患者接受了手术切除(696 例为原发性,53 例为复发性纤维瘤),243 例(18.8%)接受了药物治疗,353 例(27.3%)接受了监测。中位随访时间为 51.4 个月(范围 1-372)。749 例切除中有 696 例(92.9%)进行了原发性纤维瘤切除术,其余 53 例(7.1%)进行了复发性切除术。102 例手术治疗的患者(19%)出现了(复发)(疾病)进展,肠系膜受累是最常见的复发部位(55%)。与药物治疗后的进展相比,手术治疗后的复发有更好的结果趋势,手术治疗的患者中有 25%出现复发,而药物治疗的患者中有 50.5%出现进展[比值比 0.40(95%置信区间 0.06-2.70),p=0.35]。手术后的主要发病率为 4.4%(n=33),30 天内切除术后有 2%(n=14)的死亡率。

结论

纤维瘤病的治疗存在很大的异质性。在能够获得阴性切缘的情况下,腹部纤维瘤的手术切除仍然是一种有效的治疗选择,具有较低的主要发病率和/或死亡率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f81a/10066066/6e80111d2e25/11845_2022_3008_Fig1_HTML.jpg

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