di Franco Francesca, Baudier Thomas, Pialat Pierre Marie, Munoz Alexandre, Martinon Murielle, Pommier Pascal, Sarrut David, Biston Marie-Claude
Centre Léon Bérard, 28 rue Laennec 69373, LYON Cedex 08, France; CREATIS, CNRS UMR5220, Inserm U1044, INSA-Lyon, Université Lyon 1, Villeurbanne, France; Univ. Grenoble Alpes, CNRS, Grenoble INP, LPSC UMR5821, 38000 Grenoble, France.
Centre Léon Bérard, 28 rue Laennec 69373, LYON Cedex 08, France; CREATIS, CNRS UMR5220, Inserm U1044, INSA-Lyon, Université Lyon 1, Villeurbanne, France.
Phys Med. 2024 Feb;118:103207. doi: 10.1016/j.ejmp.2024.103207. Epub 2024 Jan 11.
To retrospectively assess the differences between planned and delivered dose during ultra-hypofractionated (UHF) prostate cancer treatments, by evaluating the dosimetric impact of daily anatomical variations alone, and in combination with prostate intrafraction motion.
Prostate intrafraction motion was recorded with a transperineal ultrasound probe in 15 patients treated by UHF radiotherapy (36.25 Gy/5 fractions). The dosimetric objective was to cover 99 % of the clinical target volume with the 100 % prescription isodose line. After treatment, planning CT (pCT) images were deformably registered onto daily Cone Beam CT to generate pseudo-CT for dose accumulation (accumulated CT, aCT). The interplay effect was accounted by synchronizing prostatic shifts and beam geometry. Finally, the shifted dose maps were accumulated (moved-accumulated CT, maCT).
No significant change in daily CTV volumes was observed. Conversely, CTV V was 98.2 ± 0.8 % and 94.7 ± 2.6 % on aCT and maCT, respectively, compared with 99.5 ± 0.2 % on pCT (p < 0.0001). Bladder volume was smaller than planned in 76 % of fractions and D was 33.8 ± 3.2 Gy and 34.4 ± 3.4 Gy on aCT (p = 0.02) and maCT (p = 0.01) compared with the pCT (36.0 ± 1.1 Gy). The rectum was smaller than planned in 50.3 % of fractions, but the dosimetric differences were not statistically significant, except for D1cc, found smaller on the maCT (33.2 ± 3.2 Gy, p = 0.02) compared with the pCT (35.3 ± 0.7 Gy).
Anatomical variations and prostate movements had more important dosimetric impact than anatomical variations alone, although, in some cases, the two phenomena compensated. Therefore, an efficient IGRT protocol is required for treatment implementation to reduce setup errors and control intrafraction motion.
通过单独评估每日解剖学变化以及结合前列腺分次内运动的剂量学影响,回顾性评估超分割(UHF)前列腺癌治疗中计划剂量与实际给予剂量之间的差异。
使用经会阴超声探头记录15例接受UHF放疗(36.25 Gy/5次分割)患者的前列腺分次内运动。剂量学目标是用100%处方等剂量线覆盖99%的临床靶区体积。治疗后,将计划CT(pCT)图像变形配准到每日锥形束CT上,以生成用于剂量累积的伪CT(累积CT,aCT)。通过同步前列腺移位和射束几何形状来考虑相互作用效应。最后,累积移位后的剂量图(移动累积CT,maCT)。
未观察到每日临床靶区体积有显著变化。相反,与pCT上的99.5±0.2%相比,aCT和maCT上临床靶区体积的V分别为98.2±0.8%和94.7±2.6%(p<0.0001)。76%的分次中膀胱体积小于计划值,与pCT(36.0±1.1 Gy)相比,aCT上的D为33.8±3.2 Gy(p=0.02),maCT上的D为34.4±3.4 Gy(p=0.01)。50.3%的分次中直肠体积小于计划值,但剂量学差异无统计学意义,除了maCT上的D1cc比pCT(35.3±0.7 Gy)小(33.2±3.2 Gy,p=0.02)。
解剖学变化和前列腺运动的剂量学影响比单纯解剖学变化更重要,尽管在某些情况下,这两种现象相互抵消。因此,治疗实施需要有效的图像引导放射治疗(IGRT)方案以减少摆位误差并控制分次内运动。