Steen R G, Spence D, Wu S, Xiong X, Kun L E, Merchant T E
Department of Diagnostic Imaging, St Jude Children's Research Hospital, Memphis, TN 38105-2794, USA.
Ann Neurol. 2001 Dec;50(6):787-95. doi: 10.1002/ana.10029.
We test a hypothesis that fractionated radiation therapy within a therapeutic dose range is associated with a dose-related change in normal brain, detectable by quantitative magnetic resonance imaging. A total of 33 patients were examined by quantitative magnetic resonance imaging to measure brain tissue spin-lattice relaxation time (T1) before treatment, and at various times during and after radiation therapy. A T1 map was generated at each time point, and radiation therapy isodose contours were superimposed on the corresponding segmented T1 map. Changes in white matter and gray matter T1 were analyzed as a function of radiation therapy dose and time since treatment, controlling for patient age and tumor site. In white matter, a dose level of more than 20 Gy was associated with a dose-dependent decrease in T1 over time, which became significant 6 months after treatment. There was no significant change in T1 of gray matter over time, at radiation therapy doses of less than 60 Gy. However, GM in close proximity to the tumor had a lower T1 before therapy. Our results represent the first radiation dose-response data derived from pediatric brain in vivo. These findings confirm that white matter is more vulnerable to radiation-induced change than is gray matter, and suggest that T1 mapping is sensitive to radiation-related changes over a broad dose range (20 to 60 Gy). Human white matter T1 is not sensitive to radiation therapy of less than 20 Gy, and gray matter T1 is unchanged over the dose range used to treat human brain tumor. The reduction of gray matter T1 near the tumor could result from compression of cortical parenchyma near the growing tumor mass, or from tumor cell invasion directly into the parenchyma. If brain T1 is a surrogate for radiation effect, reducing the volume of normal white matter receiving more than 20 Gy could be an important treatment planning goal.
我们检验了一个假设,即在治疗剂量范围内的分割放射治疗与正常脑内与剂量相关的变化有关,这种变化可通过定量磁共振成像检测到。共有33名患者接受了定量磁共振成像检查,以测量治疗前以及放射治疗期间和之后不同时间点的脑组织自旋晶格弛豫时间(T1)。在每个时间点生成T1图,并将放射治疗等剂量线轮廓叠加在相应的分割T1图上。分析白质和灰质T1的变化与放射治疗剂量和治疗后时间的函数关系,并控制患者年龄和肿瘤部位。在白质中,超过20 Gy的剂量水平与T1随时间的剂量依赖性降低相关,这种降低在治疗后6个月变得显著。在放射治疗剂量小于60 Gy时,灰质T1随时间没有显著变化。然而,靠近肿瘤的灰质在治疗前T1较低。我们的结果代表了首次从儿科脑体内获得的放射剂量反应数据。这些发现证实,白质比灰质更容易受到辐射诱导的变化影响,并表明T1映射在广泛的剂量范围(20至60 Gy)内对与辐射相关的变化敏感。人类白质T1对小于20 Gy的放射治疗不敏感,灰质T1在用于治疗人类脑肿瘤的剂量范围内没有变化。肿瘤附近灰质T1的降低可能是由于生长中的肿瘤块附近皮质实质的压缩,或者是由于肿瘤细胞直接侵入实质。如果脑T1是辐射效应的替代指标,减少接受超过20 Gy的正常白质体积可能是一个重要的治疗计划目标。