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Completed NON-SBIR/STTR RPGS NIH (US)

Radiomic biomarkers for clinical decision support that predict patient outcomes in serous ovarian carcinoma

$3M USD

Funder NATIONAL CANCER INSTITUTE
Recipient Organization H. Lee Moffitt Cancer Ctr & Res Inst
Country United States
Start Date Sep 13, 2024
End Date Aug 31, 2025
Duration 352 days
Number of Grantees 3
Roles Co-Investigator; Principal Investigator
Data Source NIH (US)
Grant ID 11172693
Grant Description

ABSTRACT Less than a third of women diagnosed with advanced epithelial ovarian cancer (EOC) survive five years after diagnosis. Despite therapeutic improvements over time, patient survival has remained relatively unchanged for decades. At present, we are unable to predict which EOC patients are at-risk for adverse outcomes following

first-line treatment. Thus, there remains a critical unmet need to identify innovative biomarkers for clinical decision support that will achieve optimal outcomes in this deadly disease. As part of standard of care (SOC) for EOC, computed tomography (CT) is used for diagnosis, prior to initiation of treatment, and to monitor treatment

response and patient outcomes. SOC CT images can be converted into quantitative data that can be used as rapid, reproducible, and accurate non-invasive biomarkers for clinical decision support in the cancer care continuum. The present proposal will utilize an extensively validated radiomics imaging pipeline developed by

our group and standard medical imaging software to measure body composition to identify image-based biomarkers that predict survival among patients with high-grade serous ovarian carcinoma (HGSOC). We will focus on HGSOC as it is the most common histotype of EOC and typically responds favorably to first-line

chemotherapy but >80% of patients experience recurrence. In Aim 1, we will build upon ongoing efforts to establish a multi-institutional cohort of racially and ethnically diverse women with HGSOC with pre-treatment SOC CT images and well-annotated clinical and outcomes data. Using validated radiomic pipelines developed

by our team, regions of interest (i.e., the primary ovarian tumor) from pre-treatment CT scans will be identified and segmented, and image features will be calculated including radiomics and body composition depots (skeletal muscle mass and subcutaneous, visceral, intra/intermuscular, and total adipose tissue). This multi-institutional

cohort will be utilized to identify and validate CT image-based features that predict survival among HGSOC patients (Aim 2). We will further test the predictive model from Aim 2 and develop de novo models among clinically relevant sub-groups of women with HGSOC, including racial and ethnic groups and women treated with

neoadjuvant chemotherapy vs. upfront surgical debulking as first-line therapy (Aim 3). This work will provide readily calculable, non-invasive biomarkers from SOC CT images for clinically translational information to better predict which patients may fail first-line therapy and to support patient therapy stratification. Ultimately, with

sufficient testing and validation, our long-term goal is to validate clinical-imaging models that could be incorporated into clinical care to improve outcomes among HGSOC patients.

All Grantees

H. Lee Moffitt Cancer Ctr & Res Inst

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