Predictive Epigenomic Biomarkers In Rectal Cancer Patients Receiving Treatment

Information

  • Research Project
  • 9271878
  • ApplicationId
    9271878
  • Core Project Number
    R01CA171767
  • Full Project Number
    5R01CA171767-05
  • Serial Number
    171767
  • FOA Number
    PA-09-204
  • Sub Project Id
  • Project Start Date
    4/1/2013 - 11 years ago
  • Project End Date
    3/31/2018 - 6 years ago
  • Program Officer Name
    THURIN, MAGDALENA
  • Budget Start Date
    4/1/2017 - 7 years ago
  • Budget End Date
    3/31/2018 - 6 years ago
  • Fiscal Year
    2017
  • Support Year
    05
  • Suffix
  • Award Notice Date
    3/30/2017 - 7 years ago

Predictive Epigenomic Biomarkers In Rectal Cancer Patients Receiving Treatment

DESCRIPTION (provided by applicant): To this day, primary rectal cancer patient management continues to be challenged by significant problems in morbidity, locoregional recurrence, and distant organ recurrence. In most studies, rectal cancer is commingled with colon cancer, yet it is clinically treated differently and molecularly distinct. Development and verification of predictive biomarkers of primary rectal tumors could significantly improve disease outcome, reduce morbidity, and most importantly improve primary rectal tumor treatment stratification. We have identified, in preliminary pilot studies, epigenomic aberrations (promoter region methylation) of non-coding genomic repeat sequences and tumor-related genes in primary rectal adenocarcinoma that are predictive biomarkers for locoregional and distant organ metastasis recurrence and disease outcome. We propose to validate these findings in primary rectal tumors from two large-scale multicenter phase III clinical trials of patients randomized between Total Mesorectal Excision surgery(TME) versus Pre-Radiotherapy followed by TME (PRTME) in a 13 yr follow-up (retrospective study), and the prospective randomized Phase III multicenter RAPIDO clinical trial of neoadjuvant chemoradiation followed by TME. Development of rectal cancer biomarkers may improve stratification into more efficient control of primary rectal tumors with and without micrometastasis. Our objective is to develop and validate a predictive biomarker panel for utility in stratifying patients for treatment. We will identify primry rectal cancer patients who could benefit from TME alone versus different approaches of neoadjuvant treatments that include radiation alone or chemoradiation regimens. The Aims are as follows: Aim I: Validate epigenomic biomarkers of primary rectal cancer to predict distant organ recurrence in TME or PRTME treated patients. Aim II: Validate epigenomic biomarkers of primary rectal cancer to predict locoregional recurrence in TME or PRTME treated patients. Aim III: Validate optimal epigenomic rectal cancer biomarkers to predict disease-free survival in neoadjuvant chemoradiation followed by TME. The study addresses an important treatment problem of primary rectal cancer using a novel combination of epigenomic predictive biomarkers.

IC Name
NATIONAL CANCER INSTITUTE
  • Activity
    R01
  • Administering IC
    CA
  • Application Type
    5
  • Direct Cost Amount
    186750
  • Indirect Cost Amount
    157430
  • Total Cost
    344180
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    394
  • Ed Inst. Type
  • Funding ICs
    NCI:344180\
  • Funding Mechanism
    Non-SBIR/STTR RPGs
  • Study Section
    CBSS
  • Study Section Name
    Cancer Biomarkers Study Section
  • Organization Name
    JOHN WAYNE CANCER INSTITUTE
  • Organization Department
  • Organization DUNS
    556074458
  • Organization City
    SANTA MONICA
  • Organization State
    CA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    904042312
  • Organization District
    UNITED STATES