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一种前瞻性部署的、用于肿瘤姑息性脊柱放射治疗的、启用深度学习的自动化质量保证工具。

A prospectively deployed deep learning-enabled automated quality assurance tool for oncological palliative spine radiation therapy.

作者信息

Kehayias Christopher E, Bontempi Dennis, Quirk Sarah, Friesen Scott, Bredfeldt Jeremy, Kosak Tara, Kearney Meghan, Tishler Roy, Pashtan Itai, Huynh Mai Anh, Aerts Hugo J W L, Mak Raymond H, Guthier Christian V

机构信息

Department of Radiation Oncology, Brigham and Women's Hospital, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.

Artificial Intelligence in Medicine (AIM) Program, Mass General Brigham, Harvard Medical School, Boston, MA, USA; Radiology and Nuclear Medicine, CARIM & GROW, Maastricht University, Maastricht, Netherlands.

出版信息

Lancet Digit Health. 2025 Jan;7(1):e13-e22. doi: 10.1016/S2589-7500(24)00243-7.

Abstract

BACKGROUND

Palliative spine radiation therapy is prone to treatment at the wrong anatomic level. We developed a fully automated deep learning-based spine-targeting quality assurance system (DL-SpiQA) for detecting treatment at the wrong anatomic level. DL-SpiQA was evaluated based on retrospective testing of spine radiation therapy treatments and prospective clinical deployment.

METHODS

The DL-SpiQA workflow involves auto-segmentation and labelling of all vertebral volumes on CT imaging using TotalSegmentator, an open-source deep learning algorithm based on nnU-Net, calculation of the radiation dose to each vertebra, and flagging and categorisation of potential treatments at the wrong anatomic level with automated email reports sent to involved radiation therapy personnel. We developed the DL-SpiQA tool based on retrospective clinical data from patients treated with palliative spine radiation therapy from sites included in the multicentre hospital network between Feb 12, 2014, and Nov 15, 2022. We used historic cases of patients who had a near-miss (ie, wrong-anatomic-level errors caught before the patient was treated) or had received wrong-anatomic-level treatment to test whether the tool could identify known errors successfully. We then used the tool prospectively over 15 months (April 24, 2023, to July 22, 2024) to evaluate any new spine radiation therapy treatment plan created for a patient, looking for any targeting errors, and dose and volume discrepancies. An email report was circulated with all the radiation therapy personnel; if any errors were found, these were highlighted and each error was defined. The tool was internally validated. All cases flagged by DL-SpiQA for both the retrospective and prospective studies were manually reviewed for dosimetric targeting, variant spine anatomy or spinal anomalies, and artificial intelligence (AI) segmentation errors. DL-SpiQA was further validated based on false positive and negative rates estimated from the retrospective results.

FINDINGS

DL-SpiQA was first tested retrospectively on 513 patients with segmentation of 10 106 vertebrae. The system raised flags for ten dose discrepancies, 49 normal anatomic variants, 49 cases with implants or other anomalies, and 20 segmentation errors (4% false positive rate). DL-SpiQA caught one historic treatment at the wrong anatomic level and three near-misses. DL-SpiQA was then prospectively deployed, reviewing 520 cases and identifying six documentation errors, which triggered detailed review by clinicians, and 43 additional cases, which confirmed clinical knowledge of variant anatomy. In all detected cases (ie, 49 of 520 cases in total), the appropriate personnel were alerted. A false negative rate of 0·03% is estimated based on the 4% AI segmentation error rate and the frequency of reported spine radiation therapy errors.

INTERPRETATION

The low false positive rate, the low false negative rate, and the high accuracy in flagging errors show that DL-SpiQA is an effective, AI-driven, automated quality assurance tool that could be used to identify anatomic spine variants and errors in targeting at the anatomic level. The tool could therefore help improve the safety of spine radiotherapy. Further external validation and tailoring is needed.

FUNDING

None.

摘要

背景

姑息性脊柱放射治疗容易出现治疗解剖层面错误。我们开发了一种基于深度学习的全自动脊柱靶向质量保证系统(DL-SpiQA),用于检测治疗解剖层面错误。基于脊柱放射治疗的回顾性测试和前瞻性临床应用对DL-SpiQA进行了评估。

方法

DL-SpiQA工作流程包括使用TotalSegmentator(一种基于nnU-Net的开源深度学习算法)对CT影像上的所有椎体体积进行自动分割和标记,计算每个椎体的放射剂量,以及通过自动电子邮件报告向相关放射治疗人员标记和分类潜在的治疗解剖层面错误。我们基于2014年2月12日至2022年11月15日多中心医院网络中接受姑息性脊柱放射治疗患者的回顾性临床数据开发了DL-SpiQA工具。我们使用有险些发生错误情况(即患者治疗前发现的解剖层面错误)或接受过解剖层面错误治疗的历史病例来测试该工具能否成功识别已知错误。然后,我们在15个月(2023年4月24日至2024年7月22日)内前瞻性地使用该工具评估为患者制定的任何新的脊柱放射治疗计划,寻找任何靶向错误以及剂量和体积差异。向所有放射治疗人员发送电子邮件报告;如果发现任何错误,将突出显示并定义每个错误。该工具进行了内部验证。对DL-SpiQA在回顾性和前瞻性研究中标记的所有病例进行人工复查,以检查剂量学靶向、脊柱解剖变异或脊柱异常以及人工智能(AI)分割错误。基于回顾性结果估计的假阳性和假阴性率对DL-SpiQA进行了进一步验证。

结果

DL-SpiQA首先对513例患者进行回顾性测试,分割了10106个椎体。该系统标记了10例剂量差异、49例正常解剖变异、49例有植入物或其他异常的病例以及20例分割错误(假阳性率为4%)。DL-SpiQA发现了1例历史上解剖层面错误的治疗病例和3例险些发生错误的情况。然后DL-SpiQA进行前瞻性应用,审查了520例病例,识别出6例文档错误,引发了临床医生的详细审查,以及43例其他病例,这些病例证实了对变异解剖的临床认识。在所有检测到的病例(即520例中的49例)中,向适当人员发出了警报。根据4%的AI分割错误率和报告的脊柱放射治疗错误频率,估计假阴性率为0.03%。

解读

低假阳性率、低假阴性率以及标记错误的高准确性表明,DL-SpiQA是一种有效的、由人工智能驱动的自动化质量保证工具,可用于识别脊柱解剖变异和解剖层面的靶向错误。因此,该工具有助于提高脊柱放疗的安全性。需要进一步的外部验证和调整。

资金来源

无。

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