Zuhir Bodalal, Eun Kyoung Hong, Stefano Trebeschi, Ieva Kurilova, Federica Landolfi, Nino Bogveradze, Francesca Castagnoli, Giovanni Randon, Petur Snaebjornsson, Filippo Pietrantonio, Jeong Min Lee, Geerard Beets, Regina Beets-Tan
{"title":"预测结直肠癌微卫星稳定性状态的无创 CT 放射生物标志物:一项多中心验证研究。","authors":"Zuhir Bodalal, Eun Kyoung Hong, Stefano Trebeschi, Ieva Kurilova, Federica Landolfi, Nino Bogveradze, Francesca Castagnoli, Giovanni Randon, Petur Snaebjornsson, Filippo Pietrantonio, Jeong Min Lee, Geerard Beets, Regina Beets-Tan","doi":"10.1186/s41747-024-00484-8","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Microsatellite instability (MSI) status is a strong predictor of response to immunotherapy of colorectal cancer. Radiogenomic approaches promise the ability to gain insight into the underlying tumor biology using non-invasive routine clinical images. This study investigates the association between tumor morphology and the status of MSI versus microsatellite stability (MSS), validating a novel radiomic signature on an external multicenter cohort.</p><p><strong>Methods: </strong>Preoperative computed tomography scans with matched MSI status were retrospectively collected for 243 colorectal cancer patients from three hospitals: Seoul National University Hospital (SNUH); Netherlands Cancer Institute (NKI); and Fondazione IRCCS Istituto Nazionale dei Tumori, Milan Italy (INT). Radiologists delineated primary tumors in each scan, from which radiomic features were extracted. Machine learning models trained on SNUH data to identify MSI tumors underwent external validation using NKI and INT images. Performances were compared in terms of area under the receiving operating curve (AUROC).</p><p><strong>Results: </strong>We identified a radiomic signature comprising seven radiomic features that were predictive of tumors with MSS or MSI (AUROC 0.69, 95% confidence interval [CI] 0.54-0.84, p = 0.018). Integrating radiomic and clinical data into an algorithm improved predictive performance to an AUROC of 0.78 (95% CI 0.60-0.91, p = 0.002) and enhanced the reliability of the predictions.</p><p><strong>Conclusion: </strong>Differences in the radiomic morphological phenotype between tumors MSS or MSI could be detected using radiogenomic approaches. Future research involving large-scale multicenter prospective studies that combine various diagnostic data is necessary to refine and validate more robust, potentially tumor-agnostic MSI radiogenomic models.</p><p><strong>Relevance statement: </strong>Noninvasive radiomic signatures derived from computed tomography scans can predict MSI in colorectal cancer, potentially augmenting traditional biopsy-based methods and enhancing personalized treatment strategies.</p><p><strong>Key points: </strong>Noninvasive CT-based radiomics predicted MSI in colorectal cancer, enhancing stratification. A seven-feature radiomic signature differentiated tumors with MSI from those with MSS in multicenter cohorts. Integrating radiomic and clinical data improved the algorithm's predictive performance.</p>","PeriodicalId":36926,"journal":{"name":"European Radiology Experimental","volume":"8 1","pages":"98"},"PeriodicalIF":3.7000,"publicationDate":"2024-08-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11347521/pdf/","citationCount":"0","resultStr":"{\"title\":\"Non-invasive CT radiomic biomarkers predict microsatellite stability status in colorectal cancer: a multicenter validation study.\",\"authors\":\"Zuhir Bodalal, Eun Kyoung Hong, Stefano Trebeschi, Ieva Kurilova, Federica Landolfi, Nino Bogveradze, Francesca Castagnoli, Giovanni Randon, Petur Snaebjornsson, Filippo Pietrantonio, Jeong Min Lee, Geerard Beets, Regina Beets-Tan\",\"doi\":\"10.1186/s41747-024-00484-8\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Microsatellite instability (MSI) status is a strong predictor of response to immunotherapy of colorectal cancer. Radiogenomic approaches promise the ability to gain insight into the underlying tumor biology using non-invasive routine clinical images. This study investigates the association between tumor morphology and the status of MSI versus microsatellite stability (MSS), validating a novel radiomic signature on an external multicenter cohort.</p><p><strong>Methods: </strong>Preoperative computed tomography scans with matched MSI status were retrospectively collected for 243 colorectal cancer patients from three hospitals: Seoul National University Hospital (SNUH); Netherlands Cancer Institute (NKI); and Fondazione IRCCS Istituto Nazionale dei Tumori, Milan Italy (INT). Radiologists delineated primary tumors in each scan, from which radiomic features were extracted. Machine learning models trained on SNUH data to identify MSI tumors underwent external validation using NKI and INT images. Performances were compared in terms of area under the receiving operating curve (AUROC).</p><p><strong>Results: </strong>We identified a radiomic signature comprising seven radiomic features that were predictive of tumors with MSS or MSI (AUROC 0.69, 95% confidence interval [CI] 0.54-0.84, p = 0.018). Integrating radiomic and clinical data into an algorithm improved predictive performance to an AUROC of 0.78 (95% CI 0.60-0.91, p = 0.002) and enhanced the reliability of the predictions.</p><p><strong>Conclusion: </strong>Differences in the radiomic morphological phenotype between tumors MSS or MSI could be detected using radiogenomic approaches. Future research involving large-scale multicenter prospective studies that combine various diagnostic data is necessary to refine and validate more robust, potentially tumor-agnostic MSI radiogenomic models.</p><p><strong>Relevance statement: </strong>Noninvasive radiomic signatures derived from computed tomography scans can predict MSI in colorectal cancer, potentially augmenting traditional biopsy-based methods and enhancing personalized treatment strategies.</p><p><strong>Key points: </strong>Noninvasive CT-based radiomics predicted MSI in colorectal cancer, enhancing stratification. A seven-feature radiomic signature differentiated tumors with MSI from those with MSS in multicenter cohorts. 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引用次数: 0
摘要
背景:微卫星不稳定性(MSI)状态是预测结直肠癌免疫疗法反应的重要指标。放射基因组学方法有望利用无创常规临床图像深入了解潜在的肿瘤生物学。本研究调查了肿瘤形态与 MSI 状态和微卫星稳定性(MSS)之间的关联,在外部多中心队列中验证了一种新型放射基因组特征:方法:回顾性收集了三家医院 243 名结直肠癌患者的术前计算机断层扫描图像,并与 MSI 状态相匹配:首尔国立大学医院(SNUH)、荷兰癌症研究所(NKI)和意大利米兰国家肿瘤研究所基金会(INT)。放射科医生在每次扫描中划定原发肿瘤,并从中提取放射学特征。使用 NKI 和 INT 图像对在 SNUH 数据上训练的机器学习模型进行外部验证,以识别 MSI 肿瘤。结果:结果:我们发现了一个由七个放射学特征组成的放射学特征,可预测MSS或MSI肿瘤(AUROC 0.69,95%置信区间[CI] 0.54-0.84,p = 0.018)。将放射学和临床数据整合到一个算法中可提高预测性能,AUROC 为 0.78 (95% CI 0.60-0.91, p = 0.002),并增强了预测的可靠性:结论:使用放射基因组学方法可以检测出MSS或MSI肿瘤在放射形态表型上的差异。未来的研究需要结合各种诊断数据进行大规模多中心前瞻性研究,以完善和验证更可靠、可能具有肿瘤诊断意义的 MSI 放射基因组模型:从计算机断层扫描中提取的无创放射基因组学特征可以预测结直肠癌中的 MSI,从而有可能增强基于活检的传统方法并加强个性化治疗策略:基于计算机断层扫描的无创放射组学可预测结直肠癌中的MSI,从而加强分层。在多中心队列中,七特征放射组学特征可将MSI肿瘤与MSS肿瘤区分开来。整合放射组学和临床数据提高了算法的预测性能。
Non-invasive CT radiomic biomarkers predict microsatellite stability status in colorectal cancer: a multicenter validation study.
Background: Microsatellite instability (MSI) status is a strong predictor of response to immunotherapy of colorectal cancer. Radiogenomic approaches promise the ability to gain insight into the underlying tumor biology using non-invasive routine clinical images. This study investigates the association between tumor morphology and the status of MSI versus microsatellite stability (MSS), validating a novel radiomic signature on an external multicenter cohort.
Methods: Preoperative computed tomography scans with matched MSI status were retrospectively collected for 243 colorectal cancer patients from three hospitals: Seoul National University Hospital (SNUH); Netherlands Cancer Institute (NKI); and Fondazione IRCCS Istituto Nazionale dei Tumori, Milan Italy (INT). Radiologists delineated primary tumors in each scan, from which radiomic features were extracted. Machine learning models trained on SNUH data to identify MSI tumors underwent external validation using NKI and INT images. Performances were compared in terms of area under the receiving operating curve (AUROC).
Results: We identified a radiomic signature comprising seven radiomic features that were predictive of tumors with MSS or MSI (AUROC 0.69, 95% confidence interval [CI] 0.54-0.84, p = 0.018). Integrating radiomic and clinical data into an algorithm improved predictive performance to an AUROC of 0.78 (95% CI 0.60-0.91, p = 0.002) and enhanced the reliability of the predictions.
Conclusion: Differences in the radiomic morphological phenotype between tumors MSS or MSI could be detected using radiogenomic approaches. Future research involving large-scale multicenter prospective studies that combine various diagnostic data is necessary to refine and validate more robust, potentially tumor-agnostic MSI radiogenomic models.
Relevance statement: Noninvasive radiomic signatures derived from computed tomography scans can predict MSI in colorectal cancer, potentially augmenting traditional biopsy-based methods and enhancing personalized treatment strategies.
Key points: Noninvasive CT-based radiomics predicted MSI in colorectal cancer, enhancing stratification. A seven-feature radiomic signature differentiated tumors with MSI from those with MSS in multicenter cohorts. Integrating radiomic and clinical data improved the algorithm's predictive performance.