Smolle Maria Anna, Leithner Andreas, Bernhardt Gerwin Alexander
Department of Orthopaedics and Trauma, Medical University of Graz, Graz 8036, Austria.
World J Clin Oncol. 2020 Feb 24;11(2):74-82. doi: 10.5306/wjco.v11.i2.74.
Despite the fact that about one third of patients with primary localized extremity soft tissue sarcoma (eSTS) will develop metastatic disease, abdominal metastases (AM) and retroperitoneal metastases (RM) constitute rare events. There is no clear consensus on how to achieve follow-up on patients with primary localized eSTS following curative resection, especially regarding the surveillance of potential AM/RM.
To systematically analyse incidence, diagnosis, treatment and outcome of AM/RM in eSTS patients.
In this systematic review, 899 studies available in PubMed and published between 2000 and 2018 were screened, identifying 17 original articles focused on AM or RM in eSTS. Article selection was based on the PRISMA guidelines, using the search terms (abdominal metastasis AND soft tissue sarcoma) and (soft tissue sarcoma metastasis abdomen). All studies published between January 1, 2000 and December 31, 2018 were screened. Further articles were identified by cross-searching article references, with the final search date being February 18, 2019. Due to limited data and the different reporting techniques used, the present review focused on descriptive analysis of the included studies.
Of the 17 studies included, six original articles reported on incidence ± diagnosis, therapy and outcome in AM and RM, whilst three original and eight case reports focused on diagnostic pathway, therapeutic procedures or outcomes without allowing conclusions regarding incidence of AM and RM. According to the former six studies, incidence of AM ranged from 0.9%-5.6% in patients with miscellaneous histological subtypes, and up to 12.1% in patients with myxoid liposarcoma. The most common histological subtypes that developed AM or RM were (myxoid) liposarcoma and leiomyosarcoma, but also rare subtypes such as epithelioid sarcoma, myxofibrosarcoma, synovial sarcoma, and malignant peripheral nerve sheath tumour had been reported to develop AM/RM. Surgery for AM/RM was performed in five of eight case-reports (62.5%) and in 20.8%-100.0% of original articles. In particular, patients with hepatic metastases undergoing metastasectomy had a survival benefit compared to patients treated with chemotherapy or best supportive care (> 3 years < 6 mo).
Patients with eSTS should undergo surveillance with abdominal ultrasonography/computed tomography, or even whole-body-magnetic resonance imaging to detect AM/RM at an early stage.
尽管约三分之一的原发性局限性肢体软组织肉瘤(eSTS)患者会发生转移性疾病,但腹部转移(AM)和腹膜后转移(RM)却很少见。对于根治性切除后的原发性局限性eSTS患者如何进行随访,尤其是关于潜在AM/RM的监测,目前尚无明确共识。
系统分析eSTS患者中AM/RM的发生率、诊断、治疗及预后。
在这项系统评价中,筛选了2000年至2018年间发表在PubMed上的899项研究,确定了17篇关注eSTS中AM或RM的原始文章。文章选择基于PRISMA指南,使用检索词(腹部转移 AND 软组织肉瘤)和(软组织肉瘤 腹部转移)。筛选了2000年1月1日至2018年12月31日期间发表的所有研究。通过交叉检索文章参考文献确定了更多文章,最终检索日期为2019年2月18日。由于数据有限且使用的报告技术不同,本综述重点对纳入研究进行描述性分析。
在纳入的17项研究中,6篇原始文章报告了AM和RM的发生率±诊断、治疗及预后,而3篇原始文章和8篇病例报告关注诊断途径、治疗程序或预后,但无法得出AM和RM发生率的结论。根据前6项研究,各种组织学亚型患者的AM发生率为0.9%-5.6%,黏液样脂肪肉瘤患者的AM发生率高达12.1%。发生AM或RM最常见的组织学亚型是(黏液样)脂肪肉瘤和平滑肌肉瘤,但也有报道称罕见亚型如上皮样肉瘤、黏液纤维肉瘤、滑膜肉瘤和恶性周围神经鞘瘤会发生AM/RM。在8篇病例报告中有5篇(62.5%)以及20.8%-100.0%的原始文章中对AM/RM进行了手术治疗。特别是,与接受化疗或最佳支持治疗的患者相比,接受肝转移灶切除术的肝转移患者有生存获益(>3年 对 <6个月)。
eSTS患者应接受腹部超声/计算机断层扫描甚至全身磁共振成像检查,以便早期发现AM/RM。