Abstract

BackgroundMagnetic resonance imaging (MRI), together with histology, is widely used to diagnose and to monitor treatment in oncology. Spatial correspondence between these modalities provides information about the ability of MRI to characterize cancerous tissue. However, registration is complicated by deformations during pathological processing, and differences in scale and information content.Methodology/Principal FindingsThis study proposes a methodology for establishing an accurate 3D relation between histological sections and high resolution in vivo MRI tumor data. The key features of the methodology are: 1) standardized acquisition and processing, 2) use of an intermediate ex vivo MRI, 3) use of a reference cutting plane, 4) dense histological sampling, 5) elastic registration, and 6) use of complete 3D data sets. Five rat pancreatic tumors imaged by T2*-w MRI were used to evaluate the proposed methodology. The registration accuracy was assessed by root mean squared (RMS) distances between manually annotated landmark points in both modalities. After elastic registration the average RMS distance decreased from 1.4 to 0.7 mm. The intermediate ex vivo MRI and the reference cutting plane shared by all three 3D images (in vivo MRI, ex vivo MRI, and 3D histology data) were found to be crucial for the accurate co-registration between the 3D histological data set and in vivo MRI. The MR intensity in necrotic regions, as manually annotated in 3D histology, was significantly different from other histologically confirmed regions (i.e., viable and hemorrhagic). However, the viable and the hemorrhagic regions showed a large overlap in T2*-w MRI signal intensity.ConclusionsThe established 3D correspondence between tumor histology and in vivo MRI enables extraction of MRI characteristics for histologically confirmed regions. The proposed methodology allows the creation of a tumor database of spatially registered multi-spectral MR images and multi-stained 3D histology.

Highlights

  • Recognizing the impact of the tumor microenvironment on oncogenic processes [1] led to the awareness that successful cancer management involves the tumor cells, and needs to target the tumor microenvironment itself

  • The proposed methodology allows the creation of a tumor database of spatially registered multi-spectral MR images and multi-stained 3D histology

  • The aim of this work is to develop a methodology for establishing an accurate 3D relation between high resolution in vivo Magnetic resonance imaging (MRI) and corresponding 3D histology of tumor tissue

Read more

Summary

Introduction

Recognizing the impact of the tumor microenvironment on oncogenic processes [1] led to the awareness that successful cancer management involves the tumor cells, and needs to target the tumor microenvironment itself. An important side effect of this process is the significant tissue deformation which inevitably changes the tumor appearance. This severely complicates the registration of in vivo MRI to histological sections. Besides the loss of the tumor 3D integrity, the registration is complicated by the inherent differences in image characteristics between color histological images and gray scale MRI images. Magnetic resonance imaging (MRI), together with histology, is widely used to diagnose and to monitor treatment in oncology. Spatial correspondence between these modalities provides information about the ability of MRI to characterize cancerous tissue. Registration is complicated by deformations during pathological processing, and differences in scale and information content

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call