Chemotherapy-Response Monitoring of Breast Cancer Patients Using Quantitative Ultrasound-Based Intra-Tumour Heterogeneities

被引:41
|
作者
Sadeghi-Naini, Ali [1 ,2 ,3 ,4 ]
Sannachi, Lakshmanan [1 ,2 ,3 ]
Tadayyon, Hadi [1 ,2 ]
Tran, William T. [3 ,5 ]
Slodkowska, Elzbieta [6 ]
Trudeau, Maureen [7 ]
Gandhi, Sonal [7 ]
Pritchard, Kathleen [7 ]
Kolios, Michael C. [8 ]
Czarnota, Gregory J. [1 ,2 ,3 ,4 ]
机构
[1] Univ Toronto, Dept Med Biophys, Toronto, ON, Canada
[2] Sunnybrook Hlth Sci Ctr, Sunnybrook Res Inst, Phys Sci, Toronto, ON, Canada
[3] Sunnybrook Hlth Sci Ctr, Dept Radiat Oncol, Odette Canc Ctr, Toronto, ON, Canada
[4] Univ Toronto, Dept Radiat Oncol, Toronto, ON, Canada
[5] Sheffield Hallam Univ, Ctr Hlth & Social Care Res, Sheffield, S Yorkshire, England
[6] Sunnybrook Hlth Sci Ctr, Div Anat Pathol, Toronto, ON, Canada
[7] Sunnybrook Hlth Sci Ctr, Div Med Oncol, Toronto, ON, Canada
[8] Ryerson Univ, Dept Phys, Toronto, ON, Canada
来源
SCIENTIFIC REPORTS | 2017年 / 7卷
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院;
关键词
BACKSCATTER COEFFICIENT MEASUREMENTS; PATHOLOGICAL COMPLETE RESPONSE; POSITRON-EMISSION-TOMOGRAPHY; DIFFUSE LIVER-DISEASE; NEOADJUVANT CHEMOTHERAPY; TEXTURE ANALYSIS; THERAPY; RADIOTHERAPY; ATTENUATION; PREDICTION;
D O I
10.1038/s41598-017-09678-0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Anti-cancer therapies including chemotherapy aim to induce tumour cell death. Cell death introduces alterations in cell morphology and tissue micro-structures that cause measurable changes in tissue echogenicity. This study investigated the effectiveness of quantitative ultrasound (QUS) parametric imaging to characterize intra-tumour heterogeneity and monitor the pathological response of breast cancer to chemotherapy in a large cohort of patients (n = 100). Results demonstrated that QUS imaging can non-invasively monitor pathological response and outcome of breast cancer patients to chemotherapy early following treatment initiation. Specifically, QUS biomarkers quantifying spatial heterogeneities in size, concentration and spacing of acoustic scatterers could predict treatment responses of patients with cross-validated accuracies of 82 +/- 0.7%, 86 +/- 0.7% and 85 +/- 0.9% and areas under the receiver operating characteristic (ROC) curve of 0.75 +/- 0.1, 0.80 +/- 0.1 and 0.89 +/- 0.1 at 1, 4 and 8 weeks after the start of treatment, respectively. The patients classified as responders and nonresponders using QUS biomarkers demonstrated significantly different survivals, in good agreement with clinical and pathological endpoints. The results form a basis for using early predictive information on survival-linked patient response to facilitate adapting standard anti-cancer treatments on an individual patient basis.
引用
收藏
页数:12
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