Development of patient-specific 3D models from histopathological samples for applications in radiation therapy

被引:5
|
作者
DeCunha, Joseph M. [1 ]
Poole, Christopher M. [2 ]
Vallieres, Martin [3 ]
Torres, Jose [4 ]
Camilleri-Broet, Sophie [4 ]
Rayes, Roni F. [5 ]
Spicer, Jonathan D. [5 ]
Enger, Shirin A. [1 ,6 ,7 ]
机构
[1] McGill Univ, Fac Med, Dept Oncol, Med Phys Unit, Montreal, PQ, Canada
[2] Radiat Analyt Pty Ltd, Sunshine Coast, Australia
[3] Univ Sherbrooke, Dept Comp Sci, Sherbrooke, PQ, Canada
[4] McGill Univ, Fac Med, Dept Pathol, Montreal, PQ, Canada
[5] McGill Univ, Canc Res Program, Dept Surg, Div Upper GI & Thorac Surg,Res Inst,Hlth Ctr, Montreal, PQ, Canada
[6] McGill Univ, Res Inst, Hlth Ctr, Montreal, PQ, Canada
[7] Jewish Gen Hosp, Lady Davis Inst Med Res, Montreal, PQ, Canada
来源
PHYSICA MEDICA-EUROPEAN JOURNAL OF MEDICAL PHYSICS | 2021年 / 81卷
关键词
Histopathology; Cellular dosimetry; Patient-specific; Microdosimetry; VOLUME FRACTION;
D O I
10.1016/j.ejmp.2020.12.009
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
The biological effects of ionizing radiation depend on the tissue, tumor type, radiation quality, and patient-specific factors. Inter-patient variation in cell/nucleus size may influence patient-specific dose response. However, this variability in dose response is not well investigated due to lack of available cell/nucleus size data. The aim of this study was to develop methods to derive cell/nucleus size distributions from digital images of 2D histopathological samples and use them to build digital 3D models for use in cellular dosimetry. Nineteen of sixty hematoxylin and eosin stained lung adenocarcinoma samples investigated passed exclusion criterion to be analyzed in the study. A difference of gaussians blob detection algorithm was used to identify nucleus centers and quantify cell spacing. Hematoxylin content was measured to determine nucleus radius. Pouring simulations were conducted to generate one-hundred 3D models containing volumes of equivalent cell spacing and nuclei radius to those in histopathological samples. The nuclei radius distributions of non-tumoral and cancerous regions appearing in the same slide were significantly different (p < 0.01) in all samples analyzed. The median nuclear-cytoplasmic ratio was 0.36 for non-tumoral cells and 0.50 for cancerous cells. The average cellular and nucleus packing densities in the 3D models generated were 65.9% (SD: 1.5%) and 13.3% (SD: 0.3%) respectively. Software to determine cell spacing and nuclei radius from histopathological samples was developed. 3D digital tissue models containing volumes with equivalent cell spacing, nucleus radius, and packing density to cancerous tissues were generated.
引用
收藏
页码:162 / 169
页数:8
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