Department of Radiation Oncology, Erasmus MC Cancer Institute, Dr. Molewaterplein 40, 3015 GD Rotterdam, The Netherlands.
Department of Radiation Oncology, Erasmus MC Cancer Institute, Dr. Molewaterplein 40, 3015 GD Rotterdam, The Netherlands.
Radiother Oncol. 2018 Dec;129(3):548-553. doi: 10.1016/j.radonc.2018.07.027. Epub 2018 Aug 31.
To explore the use of texture analysis (TA) features of patients' 3D dose distributions to improve prediction modelling of treatment complication rates in prostate cancer radiotherapy.
Late toxicity scores, dose distributions, and non-treatment related (NTR) predictors for late toxicity, such as age and baseline symptoms, of 351 patients of the hypofractionation arm of the HYPRO randomized trial were used in this study. Apart from DVH parameters, also TA features of rectum and bladder 3D dose distributions were used for predictive modelling of gastrointestinal (GI) and genitourinary (GU) toxicities. Logistic Normal Tissue Complication Probability (NTCP) models were derived, using only NTR parameters, NTR + DVH, NTR + TA, and NTR + DVH + TA.
For rectal bleeding, the area under the curve (AUC) for using only NTR parameters was 0.58, which increased to 0.68, and 0.73, when adding DVH or TA parameters respectively. For faecal incontinence, the AUC went up from 0.63 (NTR only), to 0.68 (+DVH) and 0.73 (+TA). For nocturia, adding TA features resulted in an AUC increase from 0.64 to 0.66, while no improvement was seen when including DVH parameters in the modelling. For urinary incontinence, the AUC improved from 0.68 to 0.71 (+DVH) and 0.73 (+TA). For GI, model improvements resulting from adding TA parameters to NTR instead of DVH were statistically significant (p < 0.04).
Inclusion of 3D dosimetric texture analysis features in predictive modelling of GI and GU toxicity rates in prostate cancer radiotherapy improved prediction performance, which was statistically significant for GI.
探讨使用患者 3D 剂量分布的纹理分析(TA)特征来提高前列腺癌放射治疗中治疗并发症发生率的预测模型。
本研究使用 HYPRO 随机试验的短程放疗亚组的 351 名患者的晚期毒性评分、剂量分布以及与治疗无关(NTR)的晚期毒性预测因子,如年龄和基线症状。除了剂量体积直方图(DVH)参数外,还使用直肠和膀胱 3D 剂量分布的 TA 特征来预测胃肠道(GI)和泌尿生殖系统(GU)毒性。使用仅 NTR 参数、NTR+DVH、NTR+TA 和 NTR+DVH+TA 分别推导逻辑正态组织并发症概率(NTCP)模型。
对于直肠出血,仅使用 NTR 参数的曲线下面积(AUC)为 0.58,当分别添加 DVH 或 TA 参数时,AUC 增加至 0.68 和 0.73。对于粪便失禁,AUC 从 0.63(仅 NTR)增加到 0.68(+DVH)和 0.73(+TA)。对于夜尿症,添加 TA 特征后 AUC 从 0.64 增加到 0.66,而在建模中包含 DVH 参数时则没有改善。对于尿失禁,AUC 从 0.68 增加到 0.71(+DVH)和 0.73(+TA)。对于 GI,与将 TA 参数添加到 NTR 而不是 DVH 相比,模型改进在统计学上具有显著意义(p<0.04)。
在预测前列腺癌放射治疗中 GI 和 GU 毒性发生率的模型中纳入 3D 剂量分布纹理分析特征可提高预测性能,对于 GI 具有统计学意义。