Opportunistic muscle measurements on staging chest CT for extremity and truncal soft tissue sarcoma are associated with survival

Background and Objectives Computed tomography (CT) measurements of sarcopenia have been proposed as biomarkers associated with outcomes in various cancers and have typically been evaluated at the L3 vertebral level. However, staging imaging for patients with extremity and truncal soft tissue sarcoma...

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Veröffentlicht in:Journal of surgical oncology 2020-10, Vol.122 (5), p.869-876
Hauptverfasser: Phan, Eileen N., Thorpe, Steven W., Wong, Felix S., Saiz, Augustine M., Taylor, Sandra L., Canter, Robert J., Lenchik, Leon, Randall, R. Lor, Boutin, Robert D.
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Sprache:eng
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Zusammenfassung:Background and Objectives Computed tomography (CT) measurements of sarcopenia have been proposed as biomarkers associated with outcomes in various cancers and have typically been evaluated at the L3 vertebral level. However, staging imaging for patients with extremity and truncal soft tissue sarcoma (STS) often only includes chest CT imaging which precludes evaluation at L3. Therefore, we sought to evaluate muscle metrics at T12 on standard staging chest CT scans and evaluate for correlation with overall and event‐free survival in patients with STS. Methods CT chest imaging for 89 patients with intermediate and high‐grade STS (53 male, 36 female; 58.5 ± 19.0 years old, follow‐up 37.4 ± 27.1 months) was reviewed on PACS at T12 for skeletal muscle density (SMD) and skeletal muscle index (SMI). Results Overall survival increased with increased SMD on univariate (hazard ratio [HR] = 0.61 [0.43, 0.86]) and age‐adjusted analysis (HR = 0.65 [0.42, 0.89]. Event‐free survival also increased with increased SMD in univariate analyses (HR = 0.68 [0.49, 0.95]) but did not maintain significance after adjusting for age (HR = 0.68 [0.43, 1.07]). SMI was not a predictor of overall or event‐free survival. Conclusions Higher SMD measured on routinely obtained staging chest CTs in STS patients is associated with improved survival.
ISSN:0022-4790
1096-9098
1096-9098
DOI:10.1002/jso.26077