Sabir Adeel, Schor-Bardach Rachel, Wilcox Carol J, Rahmanuddin Syed, Atkins Michael B, Kruskal Jonathan B, Signoretti Sabina, Raptopoulos Vassilios D, Goldberg S Nahum
Minimally Invasive Tumor Therapy Laboratory, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA.
AJR Am J Roentgenol. 2008 Jul;191(1):133-9. doi: 10.2214/AJR.07.2848.
The objective of our study was to determine whether perfusion CT can be used to detect early changes in therapeutic response to antiangiogenic therapy in an animal tumor model.
Twenty-five rats implanted with R3230 mammary adenocarcinoma (diameter, 1.2-2.0 cm) randomly received 7.5 or 30 mg/kg of an antiangiogenic agent, sorafenib, by daily gavage for 4 (n = 4), 9 (n = 9), or 14 (n = 5) days. Seven untreated animals served as a control group. Perfusion MDCT was performed at days 0, 4, 9, and 14 with 0.4 mL of ioversol (350 mg/mL) and included four 5-mm slices covering the entire tumor volume. Changes in tumor growth were determined by volumetric analysis of CT data. Serial changes in tumor volume and blood flow were assessed and correlated with pathology findings.
All control tumors grew larger (from 2.0 +/- 0.7 cm(3) at day 0 to 5.9 +/- 1.0 cm(3) at day 14), whereas all treated tumors shrank (from 2.5 +/- 1.1 to 2.1 +/- 1.0 cm(3)), with a statistically significant rate of growth or shrinkage in both groups (p < 0.05). Although perfusion in the control tumors changed little from day 0 to day 14 (day 0, 18.1 +/- 9.2 mL/min/100 g; day 4, 15.8 +/- 5.6; day 9, 21.7 +/- 12.2; day 14, 27.7 +/- 34), in the sorafenib group, the mean blood flow was significantly lower at day 4 (5.2 +/- 3.2 mL/min/100 g, 77% decrease), day 9 (6.4 +/- 4.0 mL/min/100 g, 66% decrease), and day 14 (6.3 +/- 5.2 mL/min/100 g, 83% decrease) compared with day 0 (23.8 +/- 11.6 mL/min/100 g) (p < 0.05). Poor correlation was seen between changes in blood flow and tumor volume for days 0-9 (r(2) = 0.34), 4-9 (r(2) = 0.0004), and 9-14 (r(2) = 0.16). However, when comparing day 4 images with days 9 and 14 images, seven of 14 (50%) sorafenib-treated tumors had focal areas of new perfusion that correlated with areas of histopathologic viability despite the fact that these tumors were shrinking in size from day 4 onward (day 4, 2.18 +/- 0.8 cm(3); day 9, 1.98 +/- 0.8 cm(3)).
Perfusion MDCT can detect focal blood flow changes even when the tumor is shrinking, possibly indicating early reversal of tumor responsiveness to antiangiogenic therapy. Given that changes in tumor volume after antiangiogenic therapy do not necessarily correlate with true treatment response, physiologic imaging of tumor perfusion may be necessary.
本研究的目的是确定灌注CT是否可用于检测动物肿瘤模型中抗血管生成治疗反应的早期变化。
25只植入R3230乳腺腺癌(直径1.2 - 2.0 cm)的大鼠随机接受7.5或30 mg/kg抗血管生成药物索拉非尼,每日灌胃,持续4天(n = 4)、9天(n = 9)或14天(n = 5)。7只未治疗的动物作为对照组。在第0、4、9和14天进行灌注MDCT检查,使用0.4 mL碘海醇(350 mg/mL),包括覆盖整个肿瘤体积的4个5 mm层面。通过CT数据的容积分析确定肿瘤生长的变化。评估肿瘤体积和血流的系列变化,并与病理结果相关联。
所有对照肿瘤均增大(从第0天的2.0±0.7 cm³增至第14天的5.9±1.0 cm³),而所有治疗组肿瘤均缩小(从2.5±1.1 cm³至2.1±1.0 cm³),两组的生长或缩小率具有统计学意义(p < 0.05)。尽管对照肿瘤从第0天到第14天灌注变化不大(第0天,18.1±9.2 mL/min/100 g;第4天,15.8±5.6;第9天,21.7±12.2;第14天,27.7±34),但在索拉非尼组中,与第0天(23.8±11.6 mL/min/100 g)相比,第4天(5.2±3.2 mL/min/100 g,降低77%)、第9天(6.4±4.0 mL/min/100 g,降低66%)和第14天(6.3±5.2 mL/min/100 g,降低83%)的平均血流显著降低(p < 0.05)。在第0 - 9天(r² = 0.34)、第4 - 9天(r² = 0.0004)和第9 - 14天(r² = 0.16),血流变化与肿瘤体积之间的相关性较差。然而,当比较第4天图像与第9天和第14天图像时,14只接受索拉非尼治疗的肿瘤中有7只(50%)有新灌注的局灶性区域,这些区域与组织病理学存活区域相关,尽管这些肿瘤从第4天起体积在缩小(第4天,2.18±0.8 cm³;第9天,1.98±0.8 cm³)。
即使肿瘤在缩小,灌注MDCT也能检测到局灶性血流变化,这可能表明肿瘤对抗血管生成治疗反应的早期逆转。鉴于抗血管生成治疗后肿瘤体积的变化不一定与真正的治疗反应相关,肿瘤灌注的生理成像可能是必要的。