Volume of Lytic Vertebral Body Metastatic Disease Quantified Using Computed Tomography-Based Image Segmentation Predicts Fracture Risk After Spine Stereotactic Body Radiation Therapy

被引:30
|
作者
Thibault, Isabelle [1 ,5 ]
Whyne, Cari M. [2 ]
Zhou, Stephanie [1 ]
Campbell, Mikki [1 ]
Atenafu, Eshetu G. [3 ]
Myrehaug, Sten [1 ]
Soliman, Hany [1 ]
Lee, Young K. [1 ]
Ebrahimi, Hamid [2 ]
Yee, Albert J. M. [4 ]
Sahgal, Arjun [1 ]
机构
[1] Univ Toronto, Sunnybrook Hlth Sci Ctr, Dept Radiat Oncol, 2075 Bayview Ave, Toronto, ON M4N 3M5, Canada
[2] Univ Toronto, Sunnybrook Res Inst, Dept Surg, Orthopaed Biomech Lab, Toronto, ON, Canada
[3] Univ Toronto, Univ Hlth Network, Dept Biostat, Toronto, ON, Canada
[4] Univ Toronto, Sunnybrook Hlth Sci Ctr, Div Orthopaed Surg, Toronto, ON, Canada
[5] Univ Laval, Ctr Hosp Univ Quebec, Dept Radiat Oncol, Quebec City, PQ, Canada
关键词
INSTABILITY NEOPLASTIC SCORE; COMPRESSION FRACTURE; QUANTITATIVE CHARACTERIZATION; RADIOTHERAPY; RADIOSURGERY; RELIABILITY; FAILURE; CANCER;
D O I
10.1016/j.ijrobp.2016.09.029
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To determine a threshold of vertebral body (VB) osteolytic or osteoblastic tumor involvement that would predict vertebral compression fracture (VCF) risk after stereotactic body radiation therapy (SBRT), using volumetric image-segmentation software. Methods and Materials: A computational semiautomated skeletal metastasis segmentation process refined in our laboratory was applied to the pretreatment planning CT scan of 100 vertebral segments in 55 patients treated with spine SBRT. Each VB was segmented and the percentage of lytic and/or blastic disease by volume determined. Results: The cumulative incidence of VCF at 3 and 12 months was 14.1% and 17.3%, respectively. The median follow-up was 7.3 months (range, 0.6-67.6 months). In all, 56% of segments were determined lytic, 23% blastic, and 21% mixed, according to clinical radiologic determination. Within these 3 clinical cohorts, the segmentation- determined mean percentages of lytic and blastic tumor were 8.9% and 6.0%, 0.2% and 26.9%, and 3.4% and 15.8% by volume, respectively. On the basis of the entire cohort (n=100), a significant association was observed for the osteolytic percentage measures and the occurrence of VCF (P<.001) but not for the osteoblastic measures. The most significant lytic disease threshold was observed at >= 11.6% (odds ratio 37.4, 95% confidence interval 9.4-148.9). On multivariable analysis, >= 11.6% lytic disease (P<.001), baseline VCF (P<.001), and SBRT with >= 20 Gy per fraction (P=.014) were predictive. Conclusions: Pretreatment lytic VB disease volumetric measures, independent of the blastic component, predict for SBRT-induced VCF. Larger-scale trials evaluating our software are planned to validate the results. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:75 / 81
页数:7
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