Retrospective audit of 957 consecutive 18F-FDG PET-CT scans compared to CT and MRI in 493 patients with different histological subtypes of bone and soft tissue sarcoma.

Clinical Sarcoma Research Pub Date : 2018-04-09 eCollection Date: 2018-01-01 DOI:10.1186/s13569-018-0095-9
Ruth E Macpherson, Sarah Pratap, Helen Tyrrell, Mehrdad Khonsari, Shaun Wilson, Max Gibbons, Duncan Whitwell, Henk Giele, Paul Critchley, Lucy Cogswell, Sally Trent, Nick Athanasou, Kevin M Bradley, A Bassim Hassan
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引用次数: 66

Abstract

Background: The use of 18F-FDG PET-CT (PET-CT) is widespread in many cancer types compared to sarcoma. We report a large retrospective audit of PET-CT in bone and soft tissue sarcoma with varied grade in a single multi-disciplinary centre. We also sought to answer three questions. Firstly, the correlation between sarcoma sub-type and grade with 18FDG SUVmax, secondly, the practical uses of PET-CT in the clinical setting of staging (during initial diagnosis), restaging (new baseline prior to definitive intervention) and treatment response. Finally, we also attempted to evaluate the potential additional benefit of PET-CT over concurrent conventional CT and MRI.

Methods: A total of 957 consecutive PET-CT scans were performed in a single supra-regional centre in 493 sarcoma patients (excluding GIST) between 2007 and 2014. We compared, PET-CT SUVmax values in relation to histology and FNCCC grading. We compared PET-CT findings relative to concurrent conventional imaging (MRI and CT) in staging, restaging and treatment responses.

Results: High-grade (II/III) bone and soft tissue sarcoma correlated with high SUVmax, especially undifferentiated pleomorphic sarcoma, leiomyosarcoma, translocation induced sarcomas (Ewing, synovial, alveolar rhabdomyosarcoma), de-differentiated liposarcoma and osteosarcoma. Lower SUVmax values were observed in sarcomas of low histological grade (grade I), and in rare subtypes of intermediate grade soft tissue sarcoma (e.g. alveolar soft part sarcoma and solitary fibrous tumour). SUVmax variation was noted in malignant peripheral nerve sheath tumours, compared to the histologically benign plexiform neurofibroma, whereas PET-CT could clearly differentiate low from high-grade chondrosarcoma. We identified added utility of PET-CT in addition to MRI and CT in high-grade sarcoma of bone and soft tissues. An estimated 21% overall potential benefit was observed for PET-CT over CT/MRI, and in particular, in 'upstaging' of high-grade disease (from M0 to M1) where an additional 12% of cases were deemed M1 following PET-CT.

Conclusions: PET-CT in high-grade bone and soft tissue sarcoma can add significant benefit to routine CT/MRI staging. Further prospective and multi-centre evaluation of PET-CT is warranted to determine the actual predictive value and cost-effectiveness of PET-CT in directing clinical management of clinically complex and heterogeneous high-grade sarcomas.

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回顾性审计493例不同组织学亚型骨和软组织肉瘤患者957次连续18F-FDG PET-CT扫描与CT和MRI扫描的对比。
背景:与肉瘤相比,18F-FDG PET-CT (PET-CT)在许多癌症类型中的应用更为广泛。我们报告了在一个多学科中心对不同级别的骨和软组织肉瘤的PET-CT的大型回顾性审计。我们还试图回答三个问题。首先,肉瘤亚型和分级与18FDG SUVmax之间的相关性,其次,PET-CT在临床分期(初始诊断期间)、再分期(最终干预前的新基线)和治疗反应中的实际应用。最后,我们还试图评估PET-CT相对于常规CT和MRI的潜在额外益处。方法:2007年至2014年间,在一个单一的超区域中心对493例肉瘤患者(GIST除外)进行了957次连续PET-CT扫描。我们比较了PET-CT SUVmax值与组织学和FNCCC分级的关系。我们比较了PET-CT与同期常规影像学(MRI和CT)在分期、再分期和治疗反应方面的表现。结果:高级别(II/III)骨和软组织肉瘤与高SUVmax相关,尤其是未分化多形性肉瘤、平滑肌肉瘤、移位性肉瘤(尤文氏肉瘤、滑膜肉瘤、肺泡横纹肌肉瘤)、去分化脂肪肉瘤和骨肉瘤。低组织学分级的肉瘤(I级)和罕见的中级软组织肉瘤亚型(如肺泡软组织肉瘤和孤立性纤维瘤)的SUVmax值较低。与组织学上良性的丛状神经纤维瘤相比,恶性周围神经鞘肿瘤的SUVmax变化明显,而PET-CT可以清楚地区分低级别和高级别软骨肉瘤。我们发现除了MRI和CT外,PET-CT在骨组织和软组织高级别肉瘤中的附加效用。与CT/MRI相比,PET-CT的总体潜在获益估计为21%,特别是在“高等级”疾病(从M0到M1)中,在PET-CT之后,另外12%的病例被认为是M1。结论:高级别骨和软组织肉瘤的PET-CT诊断可显著提高常规CT/MRI分期。需要对PET-CT进行进一步的前瞻性和多中心评估,以确定PET-CT在指导临床复杂和异质性高级别肉瘤的临床管理中的实际预测价值和成本效益。
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期刊介绍: Clinical Sarcoma Research considers for publication articles related to research on sarcomas, including both soft tissue and bone. The journal publishes original articles and review articles on the diagnosis and treatment of sarcomas along with new insights in sarcoma research, which may be of immediate or future interest for diagnosis and treatment. The journal also considers negative results, especially those from studies on new agents, as it is vital for the medical community to learn whether new agents have been proven effective or ineffective within subtypes of sarcomas. The journal also aims to offer a forum for active discussion on topics of major interest for the sarcoma community, which may be related to both research results and methodological topics.
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