Prognostic relevance of 18F-FDG PET uptake in patients with locally advanced, extremity soft tissue sarcomas undergoing neoadjuvant isolated limb perfusion with TNF-α and melphalan

被引:8
|
作者
Andreou, Dimosthenis [1 ,2 ]
Boldt, Henrike [3 ]
Pink, Daniel [4 ]
Jobke, Bjoern [5 ]
Werner, Mathias [6 ]
Schuler, Markus [7 ]
Reichardt, Peter [8 ]
Tunn, Per-Ulf [2 ]
机构
[1] Munster Univ Hosp, Dept Gen Orthoped & Tumor Orthoped, D-48149 Munster, Germany
[2] HELIOS Klinikum Berlin Buch, Dept Orthoped Oncol, Sarcoma Ctr Berlin Brandenburg, D-13125 Berlin, Germany
[3] HELIOS Klinikum Berlin Buch, Dept Nucl Med, D-13125 Berlin, Germany
[4] HELIOS Klinikum Bad Saarow, Dept Hematol Oncol & Palliat Care, Sarcoma Ctr Berlin Brandenburg, D-15526 Bad Saarow Pieskow, Germany
[5] HELIOS Klinikum Berlin Buch, Dept Radiol, D-13125 Berlin, Germany
[6] HELIOS Klinikum Emil von Behring, Sarcoma Ctr Berlin Brandenburg, Dept Pathol, D-14165 Berlin, Germany
[7] Univ Hosp Carl Gustav Carus Dresden, Dept Internal Med 1, D-01307 Dresden, Germany
[8] HELIOS Klinikum Berlin Buch, Sarcoma Ctr Berlin Brandenburg, Dept Interdisciplinary Oncol, D-13125 Berlin, Germany
关键词
Soft tissue sarcoma; Isolated limb perfusion; Response assessment; F-18-FDG PET; Prognosis; POSITRON-EMISSION-TOMOGRAPHY; ADJUVANT CHEMOTHERAPY; EVALUATE RESPONSE; RADIATION-THERAPY; GRADE; PREDICTOR; SURVIVAL; SURGERY; SIZE;
D O I
10.1007/s00259-013-2680-8
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Purpose The objective of this study was to determine whether F-18-fluorodeoxyglucose (FDG) positron emission tomography (PET) can adequately assess the risk of systemic disease progression in patients with primary, localized, high-grade soft tissue sarcomas of the extremities undergoing neoadjuvant isolated limb perfusion (ILP) with tumour necrosis factor and melphalan. Methods This was a retrospective analysis of the files of 35 patients who underwent a PET or PET/CT scan prior to and after ILP followed by surgical resection with curative intent between 2006 and 2012. SUVmax1 was defined as the maximum standardized uptake value (SUV) at diagnosis, SUVmax2 as the maximum SUV after ILP and Delta SUVmax as the percentage difference between SUVmax1 and SUVmax2. Results The median follow-up was 40 months for all patients. The median SUVmax1 amounted to 7.6, while the median SUVmax2 was 4.7. The median Delta SUVmax was -44 %. Overall survival (OS) probability at 2 and 5 years amounted to 78 and 70 %, respectively, while metastasis-free survival (MFS) probability at 2 and 5 years was 67 and 64 %, respectively. Receiver-operating characteristic (ROC) curve analysis showed that both SUVmax2 and Delta SUVmax could predict systemic disease progression, while SUVmax1 could not adequately identify patients who went on to develop metastatic disease. The optimal cut-off value was 6.9 for SUVmax2 and -31 % for Delta SUVmax. Patients with an SUVmax2 < 6.9 had a 2-year MFS of 80 %, compared to 31 % for patients with an SUVmax2 a parts per thousand yenaEuro parts per thousand 6.9 (p < 0.001). Patients with a Delta SUVmax < -31 %, i.e. patients with a higher metabolic response, had an MFS of 76 % at 2 years, compared to 42 % for patients with a Delta SUVmax a parts per thousand yenaEuro parts per thousand a'31 % (p = 0.050). Conclusion SUVmax after ILP for primary, locally advanced, non-metastatic high-grade soft tissue sarcomas of the extremities appears to be significantly correlated with prognosis. Whether patients with a high SUVmax after ILP will benefit from standard or experimental adjuvant systemic treatment options should be evaluated in future studies.
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收藏
页码:1076 / 1083
页数:8
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