Department of Radiation Oncology, Hospital of the University of Pennsylvania, Philadelphia, PA 19104, USA.
Int J Radiat Oncol Biol Phys. 2010 Nov 1;78(3):763-72. doi: 10.1016/j.ijrobp.2009.08.043. Epub 2010 Feb 18.
To assess whether whole-pelvis (WP) intensity-modulated radiation therapy (IMRT) is associated with increased toxicity compared with prostate-only (PO) IMRT.
We retrospectively analyzed all patients with prostate cancer undergoing definitive IMRT to 79.2 Gy with concurrent androgen deprivation at our institution from November 2005 to May 2007 with a minimum follow-up of 12 months. Thirty patients received initial WP IMRT to 45 Gy in 1.8-Gy fractions, and thirty patients received PO IMRT. Study patients underwent computed tomography simulation and treatment planning by use of predefined dose constraints. Bladder and rectal dose-volume histograms, maximum genitourinary (GU) and gastrointestinal (GI) Radiation Therapy Oncology Group toxicity grade, and late Grade 2 or greater toxicity-free survival curves were compared between the two groups by use of the Student t test, Fisher exact test, and Kaplan-Meier curve, respectively.
Bladder minimum dose, mean dose, median dose, volume receiving 5 Gy, volume receiving 20 Gy, volume receiving 40 Gy, and volume receiving 45 Gy and rectal minimum dose, median dose, and volume receiving 20 Gy were significantly increased in the WP group (all p values < 0.01). Maximum acute GI toxicity was limited to Grade 2 and was significantly increased in the WP group at 50% vs. 13% the PO group (p = 0.006). With a median follow-up of 24 months (range, 12-35 months), there was no difference in late GI toxicity (p = 0.884) or in acute or late GU toxicity.
Despite dosimetric differences in the volume of bowel, bladder, and rectum irradiated in the low-dose and median-dose regions, WP IMRT results only in a clinically significant increase in acute GI toxicity, in comparison to PO IMRT, with no difference in GU or late GI toxicity.
评估全骨盆(WP)调强放疗(IMRT)是否比单纯前列腺(PO)IMRT 更具毒性。
我们回顾性分析了 2005 年 11 月至 2007 年 5 月在我院接受根治性 IMRT 联合同期雄激素剥夺治疗、最低随访时间为 12 个月的前列腺癌患者。30 例患者接受初始 WP IMRT,45 Gy 分 1.8 Gy 给予,30 例患者接受 PO IMRT。研究患者通过使用预设剂量限制进行计算机断层扫描模拟和治疗计划。通过使用学生 t 检验、Fisher 确切检验和 Kaplan-Meier 曲线分别比较两组的膀胱和直肠剂量-体积直方图、最大泌尿生殖(GU)和胃肠道(GI)放射治疗肿瘤学组毒性分级以及晚期 2 级或更高的无毒性生存曲线。
WP 组的膀胱最小剂量、平均剂量、中位数剂量、5 Gy 剂量体积、20 Gy 剂量体积、40 Gy 剂量体积和 45 Gy 剂量体积,以及直肠最小剂量、中位数剂量和 20 Gy 剂量体积均显著增加(所有 p 值<0.01)。WP 组急性 GI 毒性最高限制在 2 级,显著高于 PO 组的 50%(13%)(p = 0.006)。中位随访 24 个月(范围 12-35 个月),晚期 GI 毒性无差异(p = 0.884),急性或晚期 GU 毒性无差异。
尽管 WP IMRT 照射的肠、膀胱和直肠在低剂量和中剂量区域的体积存在差异,但与 PO IMRT 相比,仅导致急性 GI 毒性显著增加,而 GU 或晚期 GI 毒性无差异。