体外生物动力成像在确定自发性非霍奇金淋巴瘤犬化疗反应中的预测价值:一项初步研究。

Convergent science physical oncology Pub Date : 2015-01-01 Epub Date: 2015-10-06 DOI:10.1088/2057-1739/1/1/015003
M R Custead, R An, J J Turek, G E Moore, D D Nolte, M O Childress
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引用次数: 11

摘要

生物动力成像(BDI)是一种新型的癌症表型分析技术,它可以光学表征活体肿瘤组织样本中亚细胞运动的变化,以响应癌症化疗药物的体外治疗。这项初步研究的目的是评估体外BDI预测10只自然发生的非霍奇金淋巴瘤狗体内化疗临床反应的能力。治疗前取所有犬的肿瘤活检样本,并用阿霉素(10 μM)体外处理。BDI在基线和药物应用后9小时定期间隔测量所有活检样本的亚细胞运动的六种动态生物标志物。随后,所有的狗都接受了阿霉素治疗它们的淋巴瘤。记录了所有狗对化疗的最佳总体反应和化疗后的无进展生存时间。受试者工作特征(ROC)曲线用于确定bdi测量的生物标志物的准确性和确定可能的临界值,这些生物标志物可以准确预测那些狗的癌症是否对阿霉素化疗有反应。一种生物标志物(指定为“MEM”)在预测阿霉素临床反应方面显示出100%的判别能力(ROC曲线下面积= 1.00,95% CI 0.692-1.000),而其他生物标志物也显示出有希望的预测能力。这些初步研究结果表明,体外BDI可以准确预测自发性动物肿瘤模型中阿霉素化疗后的治疗结果,作为一种个性化癌症治疗技术值得进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Predictive value of <i>ex vivo</i> biodynamic imaging in determining response to chemotherapy in dogs with spontaneous non-Hodgkin's lymphomas: a preliminary study.

Predictive value of <i>ex vivo</i> biodynamic imaging in determining response to chemotherapy in dogs with spontaneous non-Hodgkin's lymphomas: a preliminary study.

Predictive value of <i>ex vivo</i> biodynamic imaging in determining response to chemotherapy in dogs with spontaneous non-Hodgkin's lymphomas: a preliminary study.

Predictive value of ex vivo biodynamic imaging in determining response to chemotherapy in dogs with spontaneous non-Hodgkin's lymphomas: a preliminary study.

Biodynamic imaging (BDI) is a novel phenotypic cancer profiling technology which optically characterizes changes in subcellular motion within living tumor tissue samples in response to ex vivo treatment with cancer chemotherapy drugs. The purpose of this preliminary study was to assess the ability of ex vivo BDI to predict in vivo clinical response to chemotherapy in ten dogs with naturally-occurring non-Hodgkin's lymphomas. Pre-treatment tumor biopsy samples were obtained from all dogs and treated ex vivo with doxorubicin (10 μM). BDI measured six dynamic biomarkers of subcellular motion from all biopsy samples at baseline and at regular intervals for 9 h following drug application. All dogs subsequently received doxorubicin to treat their lymphomas. Best overall response to and progression-free survival time following chemotherapy were recorded for all dogs. Receiver operating characteristic (ROC) curves were used to determine accuracy and identify possible cut-off values for the BDI-measured biomarkers which could accurately predict those dogs' cancers that would and would not respond to doxorubicin chemotherapy. One biomarker (designated 'MEM') showed 100% discriminative capability for predicting clinical response to doxorubicin (area under the ROC curve = 1.00, 95% CI 0.692-1.000), while other biomarkers also showed promising predictive capability. These preliminary findings suggest that ex vivo BDI can accurately predict treatment outcome following doxorubicin chemotherapy in a spontaneous animal cancer model, and is worthy of further investigation as a technology for personalized cancer medicine.

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