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本文引用的文献

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Stereotactic Body Proton Therapy Versus Conventionally Fractionated Proton Therapy for Early Prostate Cancer: A Randomized, Controlled, Phase 3 Trial.立体定向体部质子治疗与常规分割质子治疗用于早期前列腺癌的疗效比较:一项随机、对照、3期试验
Int J Radiat Oncol Biol Phys. 2024 Dec 1;120(5):1377-1385. doi: 10.1016/j.ijrobp.2024.05.014. Epub 2024 Jul 6.
2
Proton therapy for the management of localized prostate cancer: Long-term clinical outcomes at a comprehensive cancer center.质子治疗用于局限性前列腺癌的管理:综合癌症中心的长期临床结果
Radiother Oncol. 2023 Nov;188:109854. doi: 10.1016/j.radonc.2023.109854. Epub 2023 Aug 18.
3
Machine-learning with region-level radiomic and dosimetric features for predicting radiotherapy-induced rectal toxicities in prostate cancer patients.基于区域水平放射组学和剂量学特征的机器学习预测前列腺癌患者放疗后直肠毒性。
Radiother Oncol. 2023 Jun;183:109593. doi: 10.1016/j.radonc.2023.109593. Epub 2023 Mar 3.
4
Predictive Model of Liver Toxicity to Aid the Personalized Selection of Proton Versus Photon Therapy in Hepatocellular Carcinoma.预测肝毒性模型以辅助肝癌质子与光子治疗的个体化选择。
Int J Radiat Oncol Biol Phys. 2023 Aug 1;116(5):1234-1243. doi: 10.1016/j.ijrobp.2023.01.055. Epub 2023 Feb 4.
5
Magnetic Resonance Imaging-Guided vs Computed Tomography-Guided Stereotactic Body Radiotherapy for Prostate Cancer: The MIRAGE Randomized Clinical Trial.磁共振成像引导与计算机断层扫描引导立体定向体部放射治疗前列腺癌:MIRAGE 随机临床试验。
JAMA Oncol. 2023 Mar 1;9(3):365-373. doi: 10.1001/jamaoncol.2022.6558.
6
NCCN Guidelines® Insights: Prostate Cancer, Version 1.2023.NCCN 指南®洞察:前列腺癌,第 1.2023 版。
J Natl Compr Canc Netw. 2022 Dec;20(12):1288-1298. doi: 10.6004/jnccn.2022.0063.
7
Protocol for development of a reporting guideline (TRIPOD-AI) and risk of bias tool (PROBAST-AI) for diagnostic and prognostic prediction model studies based on artificial intelligence.基于人工智能的诊断和预后预测模型研究报告指南(TRIPOD-AI)和偏倚风险工具(PROBAST-AI)制定方案。
BMJ Open. 2021 Jul 9;11(7):e048008. doi: 10.1136/bmjopen-2020-048008.
8
Cancer statistics for the year 2020: An overview.2020年癌症统计数据概述。
Int J Cancer. 2021 Apr 5. doi: 10.1002/ijc.33588.
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Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries.《全球癌症统计数据 2020:全球 185 个国家和地区 36 种癌症的发病率和死亡率估计》。
CA Cancer J Clin. 2021 May;71(3):209-249. doi: 10.3322/caac.21660. Epub 2021 Feb 4.
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A Deep Learning Approach Validates Genetic Risk Factors for Late Toxicity After Prostate Cancer Radiotherapy in a REQUITE Multi-National Cohort.一种深度学习方法在 REQUITE 多国队列中验证了前列腺癌放疗后迟发性毒性的遗传风险因素。
Front Oncol. 2020 Oct 15;10:541281. doi: 10.3389/fonc.2020.541281. eCollection 2020.

前列腺癌放疗后急性直肠毒性的预测模型

Predictive Model of Acute Rectal Toxicity in Prostate Cancer Treated With Radiotherapy.

作者信息

Shah Keyur D, Yeap Beow Y, Lee Hoyeon, Soetan Zainab O, Moteabbed Maryam, Muise Stacey, Cowan Jessica, Remillard Kyla, Silvia Brenda, Mendenhall Nancy P, Soffen Edward, Mishra Mark V, Kamran Sophia C, Miyamoto David T, Paganetti Harald, Efstathiou Jason A, Chamseddine Ibrahim

机构信息

Department of Radiation Oncology, Massachusetts General Hospital, Harvard Medical School, Boston, MA.

Department of Radiation Oncology, Winship Cancer Institute, Emory University, Atlanta, GA.

出版信息

JCO Clin Cancer Inform. 2025 Mar;9:e2400252. doi: 10.1200/CCI-24-00252. Epub 2025 Mar 19.

DOI:10.1200/CCI-24-00252
PMID:40106736
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11938327/
Abstract

PURPOSE

To aid personalized treatment selection, we developed a predictive model for acute rectal toxicity in patients with prostate cancer undergoing radiotherapy with photons and protons.

MATERIALS AND METHODS

We analyzed a prospective multi-institutional cohort of 278 patients treated from 2012 to 2023 across 10 centers. Dosimetric and nondosimetric variables were collected, and key predictors were identified using purposeful feature selection. The cohort was split into discovery (n = 227) and validation (n = 51) data sets. The dose along the rectum surface was transformed into a two-dimensional surface, and dose-area histograms (DAHs) were quantified. A convolutional neural network (CNN) was developed to extract dosimetric features from the DAH and integrate them with nondosimetric predictors. Model performance was benchmarked against logistic regression (LR) using the AUC.

RESULTS

Key predictors included rectum length, race, age, and hydrogel spacer use. The CNN model demonstrated stability in the discovery data set (AUC = 0.81 ± 0.11) and outperformed LR in the validation data set (AUC = 0.81 0.54). Separate analysis of photon and proton subsets yielded consistent AUCs of 0.7 and 0.92, respectively. In the photon high-risk group, the model achieved 83% sensitivity, and in proton subsets, it achieved 100% sensitivity and specificity, indicating the potential to be used for treatment selection in these patients.

CONCLUSION

Our novel approach effectively predicts rectal toxicity across photon and proton subsets, demonstrating the utility of integrating dosimetric and nondosimetric features. The model's strong performance across modalities suggests potential for guiding treatment decisions, warranting prospective validation.

摘要

目的

为辅助个性化治疗选择,我们针对接受光子和质子放疗的前列腺癌患者开发了一种急性直肠毒性预测模型。

材料与方法

我们分析了2012年至2023年期间在10个中心接受治疗的278例患者的前瞻性多机构队列。收集剂量学和非剂量学变量,并使用有目的的特征选择确定关键预测因素。该队列被分为发现数据集(n = 227)和验证数据集(n = 51)。将直肠表面的剂量转换为二维表面,并对剂量-面积直方图(DAH)进行量化。开发了一种卷积神经网络(CNN),以从DAH中提取剂量学特征,并将其与非剂量学预测因素整合。使用AUC将模型性能与逻辑回归(LR)进行基准比较。

结果

关键预测因素包括直肠长度、种族、年龄和水凝胶间隔物的使用。CNN模型在发现数据集中表现出稳定性(AUC = 0.81 ± 0.11),在验证数据集中优于LR(AUC = 0.81 0.54)。对光子和质子亚组的单独分析分别产生了一致的AUC,分别为0.7和0.92。在光子高风险组中,该模型的灵敏度达到83%,在质子亚组中,其灵敏度和特异性均达到100%,表明该模型有潜力用于这些患者的治疗选择。

结论

我们的新方法有效地预测了光子和质子亚组中的直肠毒性,证明了整合剂量学和非剂量学特征的实用性。该模型在不同模式下的强大性能表明其在指导治疗决策方面具有潜力,值得进行前瞻性验证。