Department of Radiation Oncology, University Medical Centre Utrecht, The Netherlands.
Radiother Oncol. 2009 Nov;93(2):322-30. doi: 10.1016/j.radonc.2009.08.014. Epub 2009 Sep 11.
To study the impact of MRI-guided treatment planning on dose/volume parameters in pulsed dose rate (PDR) brachytherapy (BT) for cervical cancer. Additionally, we investigated the potential benefit of an intracavitary/interstitial (IC/IS) modification of the classical tandem ovoid applicator.
For 24 patients we compared Standard PDR BT plans, Scaled Standard plans and MRI-guided Optimised plans. The total EBRT/BT prescribed dose to Manchester point A or to 90% of the HR-CTV (D90 HR-CTV) expressed in EQD(2) was 80 Gy(alphabeta10) in 17 patients (Period I) and 84 Gy(alphabeta10) in 7 patients (Period II). The constraints to 2 cm(3) of the OAR were 90 Gy(alphabeta3) for bladder and 75 Gy(alphabeta3) for rectum, sigmoid and bowel. Most cases were treated with a traditional intracavitary tandem ovoid applicator. In 6 patients we used a newly designed combined IC/IS modification for the second PDR fraction and investigated the benefit of the interstitial part.
The average gain of MRI-guided optimisation expressed in D90 HR-CTV was 4+/-9 Gy(alphabeta10) (p<0.001) and 10+/-7 Gy(alphabeta10) (p=0.003) in the two periods. The dose to 2 cm(3) of the OAR met the constraints. In the group that was treated with the combined IC/IS approach, we could increase the D90 HR-CTV for the second PDR fraction with 5.4+/-4.2 Gy(alphabeta10) (p=0.005) and the D100 with 4.8+/-3.1 Gy(alphabeta10) (p=0.07).
Three-dimensional MRI-guided treatment planning and optimisation improves the DVH parameters compared to conventional planning strategies. Additional improvement can be achieved by using a combined IC/IS approach.
研究磁共振成像(MRI)引导治疗计划对宫颈癌脉冲剂量率(PDR)近距离治疗(BT)中剂量/体积参数的影响。此外,我们还研究了经典的宫腔内/间质内(IC/IS)改良后腔内/间质内(IC/IS)应用的潜在益处。
我们对 24 例患者进行了比较,包括标准 PDR BT 计划、缩放标准计划和 MRI 引导优化计划。在两个时期(I 期和 II 期),规定剂量为曼彻斯特点 A 或 90%高风险靶区(HR-CTV)的总外照射/BT 剂量(EQD2)为 80 Gy(alpha beta10),分别有 17 例患者和 7 例患者。膀胱 OAR 2cm3 限制为 90 Gy(alpha beta3),直肠、乙状结肠和肠为 75 Gy(alpha beta3)。大多数病例采用传统的腔内宫腔内双卵圆型施源器治疗。在 6 例患者中,我们采用了新设计的 IC/IS 联合改良方法进行第二次 PDR 分次治疗,并研究了间质部分的获益。
MRI 引导优化的平均增益以 D90 HR-CTV 表示,分别为 4+/-9 Gy(alpha beta10)(p<0.001)和 10+/-7 Gy(alpha beta10)(p=0.003),在两个时期均有统计学差异。OAR 2cm3 剂量满足限制要求。在接受联合 IC/IS 方法治疗的患者中,我们可以将第二次 PDR 分次的 D90 HR-CTV 增加 5.4+/-4.2 Gy(alpha beta10)(p=0.005),D100 增加 4.8+/-3.1 Gy(alpha beta10)(p=0.07)。
与传统的计划策略相比,三维 MRI 引导治疗计划和优化可改善剂量体积直方图(DVH)参数。通过采用联合 IC/IS 方法,可进一步改善。