Department of Radiation Oncology, Academic Medical Center, Amsterdam, The Netherlands.
Radiother Oncol. 2010 Feb;94(2):248-53. doi: 10.1016/j.radonc.2009.12.011. Epub 2010 Jan 18.
To compare two methods of DVH parameter determination for combined external beam and brachytherapy treatment of cervical cancer.
Clinical treatment plans from five patients were used in this study. We simulated two applications given with PDR (32 x 60 cGy per application, given hourly) or HDR (4 x 7 Gy in two applications; each application of two fractions of 7 Gy, given within 17 h) standard and optimised treatment plans, all combined with IMRT (25 x 1.8 Gy). Additionally, we simulated an external beam (EBRT) boost to pathological lymph nodes or the parametrium (7 x 2 Gy). We determined D90 of the high-risk CTV (HR-CTV) and D(2 cc) of bladder and rectum in EQD2 in two ways. (1) 'Parameter adding': assuming a uniform contribution of the EBRT dose distribution and adding the values of DVH parameters for the two brachytherapy insertions, and (2) 'distributions adding': summing 3D biological dose distributions of IMRT and brachytherapy plans and subsequently determining the values of the DVH parameters. We took alpha/beta=10 Gy for HR-CTV, alpha/beta=3 Gy otherwise and half-time of repair 1.5 h.
Without EBRT boost, 'parameter adding' yielded a good approximation. With an EBRT boost to lymph nodes, the total D90 HR-CTV was underestimated by 2.6 (SD 1.3)% for PDR and 2.8 (SD 1.4)% for HDR. This was even worse with a parametrium boost: 9.1 (SD 6.2)% for PDR and 9.9 (SD 6.2)% for HDR.
Without an EBRT boost 'parameter adding', as proposed by the GEC-ESTRO, yielded accurate results for the values for DVH parameters. If an EBRT boost is given 'distributions adding' should be considered.
比较两种方法用于宫颈癌外照射与近距离治疗联合治疗时的剂量体积直方图(DVH)参数确定。
本研究使用了 5 例患者的临床治疗计划。我们模拟了两种应用,分别采用 PDR(每次应用 32×60cGy,每小时一次)或 HDR(两次应用各 4×7Gy,每次应用 2 个 7Gy 分次,在 17 小时内完成)标准和优化治疗计划,均联合调强放疗(IMRT,25×1.8Gy)。此外,我们还模拟了外照射(EBRT)对病理性淋巴结或宫旁组织的推量(7×2Gy)。我们以两种方式确定了高危CTV(HR-CTV)的 D90 和膀胱、直肠的 D(2cc)在 EQD2 中的值。(1)“参数相加”:假设 EBRT 剂量分布的均匀贡献,并相加两次近距离治疗插入的 DVH 参数值;(2)“分布相加”:对 IMRT 和近距离治疗计划的 3D 生物剂量分布进行求和,然后确定 DVH 参数的值。我们选择 HR-CTV 的α/β=10Gy,其他部位的α/β=3Gy,修复半衰期为 1.5 小时。
没有 EBRT 推量时,“参数相加”得到了很好的近似。对于淋巴结推量,PDR 时 HR-CTV 的总 D90 低估了 2.6%(SD 1.3%),HDR 时低估了 2.8%(SD 1.4%)。宫旁组织推量时情况更糟:PDR 时低估了 9.1%(SD 6.2%),HDR 时低估了 9.9%(SD 6.2%)。
如果没有 EBRT 推量,GEC-ESTRO 提出的“参数相加”可以为 DVH 参数值提供准确的结果。如果给予 EBRT 推量,则应考虑“分布相加”。