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使用自动化成像平台对转移性前列腺癌患者进行疾病识别、测量和时间跟踪,根据更新后的PROMISE标准进行治疗反应评估。

Treatment Response Assessment According to Updated PROMISE Criteria in Patients with Metastatic Prostate Cancer Using an Automated Imaging Platform for Identification, Measurement, and Temporal Tracking of Disease.

作者信息

Benitez Cecil M, Sahlstedt Hannicka, Sonni Ida, Brynolfsson Johan, Berenji Gholam Reza, Juarez Jesus Eduardo, Kane Nathanael, Tsai Sonny, Rettig Matthew, Nickols Nicholas George, Duriseti Sai

机构信息

Department of Radiation Oncology, University of California-Los Angeles, Los Angeles, CA, USA.

Lantheus, Lund, Sweden.

出版信息

Eur Urol Oncol. 2025 Jun;8(3):700-708. doi: 10.1016/j.euo.2024.10.011. Epub 2024 Nov 8.

Abstract

BACKGROUND AND OBJECTIVE

Prostate-specific membrane antigen (PSMA) molecular imaging is widely used for disease assessment in prostate cancer (PC). Artificial intelligence (AI) platforms such as automated Prostate Cancer Molecular Imaging Standardized Evaluation (aPROMISE) identify and quantify locoregional and distant disease, thereby expediting lesion identification and standardizing reporting. Our aim was to evaluate the ability of the updated aPROMISE platform to assess treatment responses based on integration of the RECIP (Response Evaluation Criteria in PSMA positron emission tomography-computed tomography [PET/CT]) 1.0 classification.

METHODS

The study included 33 patients with castration-sensitive PC (CSPC) and 34 with castration-resistant PC (CRPC) who underwent PSMA-targeted molecular imaging before and ≥2 mo after completion of treatment. Tracer-avid lesions were identified using aPROMISE for pretreatment and post-treatment PET/CT scans. Detected lesions were manually approved by an experienced nuclear medicine physician, and total tumor volume (TTV) was calculated. Response was assessed according to RECIP 1.0 as CR (complete response), PR (partial response), PD (progressive disease), or SD (stable disease). KEY FINDINGS AND LIMITATIONS: aPROMISE identified 1576 lesions on baseline scans and 1631 lesions on follow-up imaging, 618 (35%) of which were new. Of the 67 patients, aPROMISE classified four as CR, 16 as PR, 34 as SD, and 13 as PD; five cases were misclassified. The agreement between aPROMISE and clinician validation was 89.6% (κ = 0.79).

CONCLUSIONS AND CLINICAL IMPLICATIONS

aPROMISE may serve as a novel assessment tool for treatment response that integrates PSMA PET/CT results and RECIP imaging criteria. The precision and accuracy of this automated process should be validated in prospective clinical studies.

PATIENT SUMMARY

We used an artificial intelligence (AI) tool to analyze scans for prostate cancer before and after treatment to see if we could track how cancer spots respond to treatment. We found that the AI approach was successful in tracking individual tumor changes, showing which tumors disappeared, and identifying new tumors in response to prostate cancer treatment.

摘要

背景与目的

前列腺特异性膜抗原(PSMA)分子成像广泛应用于前列腺癌(PC)的疾病评估。诸如自动化前列腺癌分子成像标准化评估(aPROMISE)等人工智能(AI)平台可识别并量化局部和远处疾病,从而加快病灶识别并规范报告。我们的目的是评估更新后的aPROMISE平台基于整合RECIP(PSMA正电子发射断层扫描-计算机断层扫描[PET/CT]反应评估标准)1.0分类来评估治疗反应的能力。

方法

该研究纳入了33例去势敏感型PC(CSPC)患者和34例去势抵抗型PC(CRPC)患者,这些患者在治疗前及治疗完成后≥2个月接受了PSMA靶向分子成像检查。使用aPROMISE对治疗前和治疗后的PET/CT扫描进行示踪剂摄取病灶的识别。检测到的病灶由经验丰富的核医学医师进行人工核准,并计算总肿瘤体积(TTV)。根据RECIP 1.0将反应评估为CR(完全缓解)、PR(部分缓解)、PD(疾病进展)或SD(疾病稳定)。主要发现与局限性:aPROMISE在基线扫描中识别出1576个病灶,在随访成像中识别出1631个病灶,其中618个(35%)为新病灶。在67例患者中,aPROMISE将4例分类为CR,16例为PR,34例为SD,13例为PD;5例分类错误。aPROMISE与临床医生验证之间的一致性为89.6%(κ = 0.79)。

结论与临床意义

aPROMISE可作为一种整合PSMA PET/CT结果和RECIP成像标准的新型治疗反应评估工具。这一自动化流程的精确性和准确性应在前瞻性临床研究中得到验证。

患者总结

我们使用一种人工智能(AI)工具分析前列腺癌治疗前后的扫描结果,以查看我们是否能够追踪癌灶对治疗的反应。我们发现,AI方法成功地追踪了个体肿瘤变化,显示出哪些肿瘤消失,并识别出前列腺癌治疗后出现的新肿瘤。

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