Clinical Trials Directory

Trials / Unknown

UnknownNCT00601406

Study of DNA Mutations in Predicting the Effect of External-Beam Radiation Therapy in Patients With Early Breast Cancer, Localized Prostate Cancer, or Gynecological Cancer

Radiogenomics: Assessment of Polymorphisms for Predicting the Effects of Radiotherapy (RAPPER)

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
2,200 (estimated)
Sponsor
The Christie NHS Foundation Trust · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

RATIONALE: Studying samples of blood from patients with cancer in the laboratory may help doctors learn more about changes that occur in DNA and identify biomarkers related to cancer. It may also help doctors predict how patients will respond to treatment. PURPOSE: This clinical trial is evaluating DNA mutations in predicting the effect of external-beam radiation therapy in patients with early breast cancer, localized prostate cancer, or gynecologic cancer.

Detailed description

OBJECTIVES: Primary * To test the hypothesis that an association between common genetic variations, reported by single nucleotide polymorphisms (SNP) in relevant candidate genes, is associated with individual patient variability in normal tissue radiation response and toxicity. Secondary * To compare different clinical scoring systems for late normal tissue effects, specifically Late Effect of Normal Tissue Subjective Objective Management Analysis (LENT SOMA), Radiation Therapy Oncology Group (RTOG), quality of life, and in a subset common terminology criteria (CTC) version 3. * To compare clinical scoring systems with analytical measures of normal tissue outcome in a minority of patients, using volume change in the breast measured by laser camera. * To correlate family history information with SNP analysis to produce a polymorphism risk score (PRS) for family history. * To compare a detailed 3D dose-volume analysis in a subset of patients with late effects and SNP results. * To correlate actuarial analysis of late effects changes over time with PRS. * To conduct PRS analyses against tumor control probability (TCP), using survival as a surrogate for TCP where necessary, and normal tissue complications vs tumor control probability. OUTLINE: This is a multicenter study. Patients are recruited from clinical trials in which their late normal tissue effects have been measured. Blood samples are collected from these patients for analysis of genetic variation by DNA extraction and single nucleotide polymorphism analysis. Sixty different genes, including those involved in cell cycle checkpoint control, DNA damage recognition and repair, induction of apoptosis, and cytokine production (including TGFβ pathways) are assessed.

Conditions

Interventions

TypeNameDescription
GENETICgene expression analysis
GENETICgene rearrangement analysis
GENETICpolymorphism analysis
OTHERlaboratory biomarker analysis
RADIATIONradiation therapy

Timeline

Start date
2006-03-01
Primary completion
2008-02-01
First posted
2008-01-28
Last updated
2013-08-26

Locations

11 sites across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT00601406. Inclusion in this directory is not an endorsement.