Ahmad Sarfraz, Stevenson Jonathan, Mangham Charles, Cribb Gillian, Cool Paul
Department of Musculoskeletal Oncology, Robert Jones and Agnes Hunt Orthopaedic Hospital, Oswestry, Shropshire, SY10 7AG, UK,
Skeletal Radiol. 2014 Dec;43(12):1679-86. doi: 10.1007/s00256-014-1979-2. Epub 2014 Aug 14.
Assessment of the extent of tumours using magnetic resonance imaging (MRI) is the basis for bone resection in limb-salvage surgery. We aimed to compare the accuracy of T1-weighted MRI and STIR sequences in measuring the extent of proximal femoral tumours, using the macroscopic specimens as the gold standard for comparison.
We compared single coronal T1-weighted with STIR sequences in 34 proximal femoral tumours, using bivalved resected macroscopic tumours for comparison. After randomisation, four observers measured longitudinal osseous tumour extent using MRI and specimen photographs on two separate occasions, 3 weeks apart.
There were 25 metastatic tumours, 8 chondrosarcomas and 1 myeloma. Eight patients presented with pathological fractures. The Pearson's correlation coefficient for comparison of T1 with macroscopic tumours was 0.91 (95% confidence interval [CI]: 0.83 to 0.96) for all observers and 0.90 (95% CI: 0.81 to 0.95) for STIR images. This difference was not statistically significant, and T1 and STIR sequence measurements had similar precision and accuracy. Bland-Altman plots showed T1-weighted imaging to be unbiased, whereas STIR sequences were biased and had systematic error. Moreover, STIR measurements overestimated tumour size by 6.4 mm (95% CI: -26.9 to 39.7 mm) and 2 patients were outliers. T1 measurements were closer to the macroscopic measurements with a mean difference of 1.3 mm (95% CI: -28.9 mm to 31.5 mm), with 3 patients falling outside of this. The variance was greater for STIR measurements. This difference between T1 and STIR measurements was statistically significant (p = 0.000003). The intra-observer reliability between separate measurements for MRI and specimen photographs achieved interclass correlation coefficients of 0.97, 0.96 and 0.95 (T1, STIR and macroscopic tumour respectively). T1 had greater interobserver correlation than for STIR and macroscopic tumour measurements (0.88 vs 0.85 and 0.85 respectively). These differences in interclass correlation were not statistically significant.
This study has shown T1-weighted MRI sequences to be unbiased compared with STIR sequences at determining intra-osseous tumour extent. STIR overestimates the length of bone tumours. T1 is therefore preferred for pre-operative planning for the resection of bone tumours.
利用磁共振成像(MRI)评估肿瘤范围是保肢手术中骨切除的基础。我们旨在以大体标本作为比较的金标准,比较T1加权MRI和短反转恢复(STIR)序列在测量股骨近端肿瘤范围方面的准确性。
我们对34例股骨近端肿瘤的单冠位T1加权序列与STIR序列进行了比较,使用二分切除的大体肿瘤作为对照。随机分组后,四名观察者在两个不同时间(间隔3周)使用MRI和标本照片测量骨肿瘤的纵向范围。
有25例转移性肿瘤、8例软骨肉瘤和1例骨髓瘤。8例患者出现病理性骨折。所有观察者T1与大体肿瘤比较的Pearson相关系数为0.91(95%置信区间[CI]:0.83至0.96),STIR图像为0.90(95%CI:0.81至0.95)。这种差异无统计学意义,T1和STIR序列测量具有相似的精密度和准确性。Bland-Altman图显示T1加权成像无偏差,而STIR序列有偏差且存在系统误差。此外,STIR测量高估肿瘤大小6.4毫米(95%CI:-26.9至39.7毫米),2例患者为离群值。T1测量更接近大体测量,平均差异为1.3毫米(95%CI:-28.9毫米至31.5毫米),3例患者超出此范围。STIR测量的方差更大。T1和STIR测量之间的这种差异具有统计学意义(p = 0.000003)。MRI和标本照片单独测量之间的观察者内可靠性达到组内相关系数分别为0.97、0.96和0.95(分别为T1、STIR和大体肿瘤)。T1的观察者间相关性高于STIR和大体肿瘤测量(分别为0.88对0.85和0.85)。这些组内相关的差异无统计学意义。
本研究表明,在确定骨内肿瘤范围方面,与STIR序列相比,T1加权MRI序列无偏差。STIR高估了骨肿瘤的长度。因此,T1更适合用于骨肿瘤切除的术前规划。