R01CA260003
Project Grant
Overview
Grant Description
Imaging-based tumor forecasting to predict brain tumor progression and response to therapy - The vision for this program is to develop tumor forecasting methods to predict and optimize the response of glioblastoma multiforme to standard-of-care therapies—and do so on a tumor-specific basis.
A fundamental challenge in the care of patients with brain tumors is the limitation of standard radiographic methods to accurately evaluate, let alone predict, patient response. We propose to address this shortcoming by developing predictive, biologically-based mathematical models that incorporate the hallmark characteristics of brain tumor growth (e.g., tumor induced angiogenesis, hypoxia, necrosis, proliferation, invasion, and resistance to therapy) that can be initialized using advanced, subject-specific imaging data.
This project will address two critical gaps in the care of patients battling brain cancer. First, our imaging-based, mathematical framework accounts for subject-specific characteristics and treatment regimens on model predictions. Second, in most studies, the ground truth used for validation of the predictive model is whether the model can predict future regional contrast enhancement, despite the well-known limitations of this qualitative MRI feature.
Thus, while prior human studies have demonstrated the potential of predictive modeling, its translation into a realistic radiologic tool is fundamentally hindered by lack of systematic, pre-clinical validation where critical tumor characteristics (e.g., tumor heterogeneity and whole brain tumor cell distribution) can be precisely known and rigorously controlled.
To overcome these limitations, we aim to: 1) establish the accuracy of tumor-specific modeling to predict spatiotemporal progression and 2) establish the accuracy of tumor-specific modeling to predict therapeutic response.
Experimentally, we will construct a family of mathematical models that employ quantitative MRI data to capture the fundamental biological features of glioblastoma. These data are longitudinally acquired in patient derived xenografts that are treatment naïve or undergoing radiotherapy and/or chemotherapy. The model family is then calibrated with these data and a novel model selection strategy is employed to choose the most parsimonious model for predicting the spatio-temporal evolution of each tumor which is then compared to MRI data collected at future time points.
Model predictions of tumor progression will be validated via registration to 3D fluorescent images of cleared ex vivo tissue, a technique that enables visualization of whole brain tumor burden.
We will provide the clinical and scientific community with a validated mathematical description of glioma progression that can reliably predict progression and therapy response across a range of relevant glioma signaling pathways and can be readily applied to the clinical setting.
A fundamental challenge in the care of patients with brain tumors is the limitation of standard radiographic methods to accurately evaluate, let alone predict, patient response. We propose to address this shortcoming by developing predictive, biologically-based mathematical models that incorporate the hallmark characteristics of brain tumor growth (e.g., tumor induced angiogenesis, hypoxia, necrosis, proliferation, invasion, and resistance to therapy) that can be initialized using advanced, subject-specific imaging data.
This project will address two critical gaps in the care of patients battling brain cancer. First, our imaging-based, mathematical framework accounts for subject-specific characteristics and treatment regimens on model predictions. Second, in most studies, the ground truth used for validation of the predictive model is whether the model can predict future regional contrast enhancement, despite the well-known limitations of this qualitative MRI feature.
Thus, while prior human studies have demonstrated the potential of predictive modeling, its translation into a realistic radiologic tool is fundamentally hindered by lack of systematic, pre-clinical validation where critical tumor characteristics (e.g., tumor heterogeneity and whole brain tumor cell distribution) can be precisely known and rigorously controlled.
To overcome these limitations, we aim to: 1) establish the accuracy of tumor-specific modeling to predict spatiotemporal progression and 2) establish the accuracy of tumor-specific modeling to predict therapeutic response.
Experimentally, we will construct a family of mathematical models that employ quantitative MRI data to capture the fundamental biological features of glioblastoma. These data are longitudinally acquired in patient derived xenografts that are treatment naïve or undergoing radiotherapy and/or chemotherapy. The model family is then calibrated with these data and a novel model selection strategy is employed to choose the most parsimonious model for predicting the spatio-temporal evolution of each tumor which is then compared to MRI data collected at future time points.
Model predictions of tumor progression will be validated via registration to 3D fluorescent images of cleared ex vivo tissue, a technique that enables visualization of whole brain tumor burden.
We will provide the clinical and scientific community with a validated mathematical description of glioma progression that can reliably predict progression and therapy response across a range of relevant glioma signaling pathways and can be readily applied to the clinical setting.
Funding Goals
TO IMPROVE SCREENING AND EARLY DETECTION STRATEGIES AND TO DEVELOP ACCURATE DIAGNOSTIC TECHNIQUES AND METHODS FOR PREDICTING THE COURSE OF DISEASE IN CANCER PATIENTS. SCREENING AND EARLY DETECTION RESEARCH INCLUDES DEVELOPMENT OF STRATEGIES TO DECREASE CANCER MORTALITY BY FINDING TUMORS EARLY WHEN THEY ARE MORE AMENABLE TO TREATMENT. DIAGNOSIS RESEARCH FOCUSES ON METHODS TO DETERMINE THE PRESENCE OF A SPECIFIC TYPE OF CANCER, TO PREDICT ITS COURSE AND RESPONSE TO THERAPY, BOTH A PARTICULAR THERAPY OR A CLASS OF AGENTS, AND TO MONITOR THE EFFECT OF THE THERAPY AND THE APPEARANCE OF DISEASE RECURRENCE. THESE METHODS INCLUDE DIAGNOSTIC IMAGING AND DIRECT ANALYSES OF SPECIMENS FROM TUMOR OR OTHER TISSUES. SUPPORT IS ALSO PROVIDED FOR ESTABLISHING AND MAINTAINING RESOURCES OF HUMAN TISSUE TO FACILITATE RESEARCH. SMALL BUSINESS INNOVATION RESEARCH (SBIR) PROGRAM: TO EXPAND AND IMPROVE THE SBIR PROGRAM, TO INCREASE PRIVATE SECTOR COMMERCIALIZATION OF INNOVATIONS DERIVED FROM FEDERAL RESEARCH AND DEVELOPMENT, TO INCREASE SMALL BUSINESS PARTICIPATION IN FEDERAL RESEARCH AND DEVELOPMENT, AND TO FOSTER AND ENCOURAGE PARTICIPATION OF SOCIALLY AND ECONOMICALLY DISADVANTAGED SMALL BUSINESS CONCERNS AND WOMEN-OWNED SMALL BUSINESS CONCERNS IN TECHNOLOGICAL INNOVATION. SMALL BUSINESS TECHNOLOGY TRANSFER (STTR) PROGRAM: TO STIMULATE AND FOSTER SCIENTIFIC AND TECHNOLOGICAL INNOVATION THROUGH COOPERATIVE RESEARCH AND DEVELOPMENT CARRIED OUT BETWEEN SMALL BUSINESS CONCERNS AND RESEARCH INSTITUTIONS, TO FOSTER TECHNOLOGY TRANSFER BETWEEN SMALL BUSINESS CONCERNS AND RESEARCH INSTITUTIONS, TO INCREASE PRIVATE SECTOR COMMERCIALIZATION OF INNOVATIONS DERIVED FROM FEDERAL RESEARCH AND DEVELOPMENT, AND TO FOSTER AND ENCOURAGE PARTICIPATION OF SOCIALLY AND ECONOMICALLY DISADVANTAGED SMALL BUSINESS CONCERNS AND WOMEN-OWNED SMALL BUSINESS CONCERNS IN TECHNOLOGICAL INNOVATION.
Grant Program (CFDA)
Awarding / Funding Agency
Place of Performance
Houston,
Texas
770304009
United States
Geographic Scope
Single Zip Code
Related Opportunity
Analysis Notes
Amendment Since initial award the End Date has been extended from 08/31/27 to 08/31/28 and the total obligations have increased 369% from $684,353 to $3,208,620.
The Univeristy Of Texas M.D. Anderson Cancer Center was awarded
Advanced Imaging-Based Brain Tumor Forecasting Therapy Optimization
Project Grant R01CA260003
worth $3,208,620
from National Cancer Institute in September 2022 with work to be completed primarily in Houston Texas United States.
The grant
has a duration of 6 years and
was awarded through assistance program 93.394 Cancer Detection and Diagnosis Research.
The Project Grant was awarded through grant opportunity NIH Research Project Grant (Parent R01 Clinical Trial Not Allowed).
Status
(Ongoing)
Last Modified 9/24/25
Period of Performance
9/19/22
Start Date
8/31/28
End Date
Funding Split
$3.2M
Federal Obligation
$0.0
Non-Federal Obligation
$3.2M
Total Obligated
Activity Timeline
Transaction History
Modifications to R01CA260003
Additional Detail
Award ID FAIN
R01CA260003
SAI Number
R01CA260003-4005740721
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Public/State Controlled Institution Of Higher Education
Awarding Office
75NC00 NIH National Cancer Institute
Funding Office
75NC00 NIH National Cancer Institute
Awardee UEI
S3GMKS8ELA16
Awardee CAGE
0KD38
Performance District
TX-09
Senators
John Cornyn
Ted Cruz
Ted Cruz
Budget Funding
Federal Account | Budget Subfunction | Object Class | Total | Percentage |
---|---|---|---|---|
National Cancer Institute, National Institutes of Health, Health and Human Services (075-0849) | Health research and training | Grants, subsidies, and contributions (41.0) | $1,331,382 | 100% |
Modified: 9/24/25