Previous Page  14 / 28 Next Page
Information
Show Menu
Previous Page 14 / 28 Next Page
Page Background

Notes:

Page 40

Medical Imaging 2016

October 20-21, 2016

Volume 5, Issue 5(Suppl)

OMICS J Radiol

ISSN: 2167-7964 ROA, an open access journal

conferenceseries

.com

October 20-21, 2016 Chicago, USA

International Conference on

Medical Imaging & Diagnosis

Bin Zheng, OMICS J Radiol 2016, 6:5(Suppl)

http://dx.doi.org/10.4172/2167-7964.C1.009

Applying computer-aided detection schemes to assist predicting response of ovarian cancer patients

to chemotherapy in clinical trials

Bin Zheng

University of Oklahoma, USA

T

he majority of ovarian cancer cases are diagnosed at late stage and it has the highest mortality rate among gynecologic

malignancies. Thus, applying effective chemotherapy is important for reducing patients’ mortality rate. A principle

challenge in treating ovarian cancer is that no biomarker exists to date to reliably select treatment options, predict clinical

benefit, and determine drug resistance. In our group, we developed and tested several computer-aided detection (CAD)

schemes, which aim to more accurately predict response of ovarian cancer patients to chemotherapy at an early stage using CT

images acquired either pre-therapy, post-therapy or both. In this presentation, I will discuss 4 recent studies, which include (1)

developing a B-spline based deformable image registration scheme to automatically detect more tumors that have significant

volume and density changes depicting in pre- and post-therapy CT images, (2) segmenting targeted tumors and quantifying

image feature change between the pre- and post-therapy CT images, (3) detecting non-tumor based quantitative image features

and (4) testing the feasibility of using tumor image features computed from pre-therapy CT images only to predict progression-

free survival (PFS). From our experimental results, we made following observations. First, using CAD schemes, we enabled to

detect more clinically-relevant tumors that have impact on PFS. Second, it is feasible to predict PFS of patients who participated

in the clinical trials at an early stage (i.e., 6 weeks after starting therapy). Third, quantifying some non-tumor (i.e., adiposity)

features can play a useful role to predict patients’ PFS. Last, using tumor features computed from pre-therapy CT images

only also provide discriminatory information to predict PFS. However, using the features difference computed pre- and post-

therapy CT still yielded higher prediction accuracy. In conclusion, we demonstrated that applying CAD schemes has potential

to assist developing more effective personalized cancer treatment strategy in the future.

Biography

Bin Zheng has experience in developing and evaluating computer-aided quantitative medical image analysis schemes for more than 20 years. Currently, his

computer-aided diagnosis laboratory is working on the following research areas: (1) Identify quantitative image feature markers and develop machine learning

classifiers or statistical models to help predict or assess cancer risk and prognosis (i.e., breast, lung and ovarian cancer); (2) develop interactive CAD schemes

and workstation using content-based image retrieval (CBIR) approach to assist radiologists in cancer diagnosis (classify between malignant and benign lesions);

(3) develop new electrical impedance spectroscopy (EIS) technology to assist cancer screening (e.g., breast) and/or lesion classification (e.g., thyroid nodules).

bin.zheng-1@ou.edu