CR-UK and EPSRC Cancer Imaging Centre, Institute of Cancer Research and Royal Marsden NHS Foundation Trust, Sutton, Surrey, UK.
Cancer Biomark. 2010;7(4):201-10. doi: 10.3233/CBM-2010-0194.
This study correlates apparent diffusion coefficients (ADCs) from Diffusion-weighted Imaging (DWI) in primary ovarian tumours and their omental metastases following neoadjuvant chemotherapy with epithelial and stromal densities in order to relate them to histological composition. Eight patients underwent DWI at 1.5 T with four b-values (0, 600, 900, and 1,050 s/mm(2))at baseline and after one and three cycles of platinum-based chemotherapy. Mean ADCs were calculated at each timepoint from solid tumour at ovarian and omental sites. Specimens from 15 corresponding lesions (8 ovarian, 7 omental), obtained at interval debulking surgery, were stained immunohistochemically to quantify epithelial and stromal components. End-of-treatment ADC was correlated with epithelial and stromal densities. Longitudinal changes in ADC with treatment were compared between primary and metastatic lesions using parametric tests. No baseline differences in ADC between primary and metastatic sites were seen. Mean ADC increased significantly from baseline after both first and third cycle (P < 0.001) in both ovarian and omental lesions. ADC and total epithelial plus stromal density (lesion cellularity) were negatively correlated in ovarian lesions (r= -0.79, P=0.02) but not in omental metastases or when both sites were considered together. However, ADC and epithelial density were negatively correlated in ovarian (r=- 0.78, P=0.02) and omental lesions (r=-0.75, P=0.04) and when both sites were considered together (r=-0.77, P< 0.001). There was no significant correlation between ADC and stromal density. Thus ADC reflects mainly epithelial content in advanced ovarian cancer and is not solely a function of lesion cellularity.
本研究将原发性卵巢肿瘤及其新辅助化疗后的网膜转移瘤的弥散加权成像(DWI)表观扩散系数(ADC)与其上皮和间质密度相关联,以将其与组织学成分相关联。8 名患者在 1.5 T 下进行 DWI 检查,共进行 4 次 b 值(0、600、900 和 1050 s/mm²),分别在基线时和 1 个和 3 个铂类化疗周期后进行。在卵巢和网膜部位的实性肿瘤处计算每个时间点的平均 ADC。在间隔性减瘤手术时获得 15 个相应病变(8 个卵巢,7 个网膜)的标本,用免疫组织化学染色定量上皮和间质成分。治疗结束时的 ADC 与上皮和间质密度相关。使用参数检验比较原发性和转移性病变治疗前后 ADC 的纵向变化。原发性和转移性部位的基线 ADC 无差异。卵巢和网膜病变的初次和第三次周期后,ADC 均显著高于基线(P < 0.001)。在卵巢病变中,ADC 与总上皮加间质密度(病变细胞密度)呈负相关(r=-0.79,P=0.02),但在网膜转移或同时考虑两者时则不然。然而,在卵巢(r=-0.78,P=0.02)和网膜病变(r=-0.75,P=0.04)以及同时考虑两者时,ADC 与上皮密度呈负相关(r=-0.77,P<0.001)。ADC 与间质密度之间无显著相关性。因此,ADC 主要反映晚期卵巢癌中的上皮含量,而不仅仅是病变细胞密度的函数。