Duvvuri U, Poptani H, Feldman M, Nadal-Desbarats L, Gee M S, Lee W M, Reddy R, Leigh J S, Glickson J D
Department of Radiology, University of Pennsylvania, Philadelphia, Pennsylvania 19104-6100, USA.
Cancer Res. 2001 Nov 1;61(21):7747-53.
This study compares two potential magnetic resonance imaging (MRI) indices for noninvasive early detection of tumor response to chemotherapy: the spin-lattice relaxation in the rotating frame (T1rho) and the transverse relaxation time (T2). Measurements of these relaxation parameters were performed on a s.c. murine radiation-induced fibrosarcoma (RIF-1) model before and after cyclophosphamide treatment. The number of pixels exhibiting T1rho values longer than controls in viable regions of the tumor increased significantly as early as 18 h after drug administration and remained elevated up to 36 h after treatment (P < 0.005). Although a trend of increasing T2s relative to controls was noted in viable regions of the tumor 36 h after treatment, the changes were not statistically significant. Histological examination indicated a decrease in mitotic index that paralleled the changes in T1rho. We conclude that T1rho measurements may be useful for noninvasive monitoring of early response of tumors to chemotherapy.
本研究比较了两种用于肿瘤化疗反应无创早期检测的潜在磁共振成像(MRI)指标:旋转坐标系中的自旋晶格弛豫时间(T1rho)和横向弛豫时间(T2)。在环磷酰胺治疗前后,对皮下小鼠辐射诱导纤维肉瘤(RIF-1)模型进行了这些弛豫参数的测量。给药后18小时,肿瘤存活区域中T1rho值长于对照的像素数量即显著增加,并在治疗后36小时内持续升高(P < 0.005)。尽管治疗后36小时在肿瘤存活区域观察到相对于对照T2有增加趋势,但变化无统计学意义。组织学检查显示有丝分裂指数降低,与T1rho变化平行。我们得出结论,T1rho测量可能有助于对肿瘤化疗早期反应进行无创监测。