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Pilot Study of Biomarkers for Radiation Therapy

Investigating Proteomic Biomarkers of Radiation Therapy Outcome: A Pilot Study

Status
Suspended
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01050725
Enrollment
100
Registered
2010-01-15
Start date
2009-11-30
Completion date
Unknown
Last updated
2011-06-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer

Keywords

proteome, biomarkers, radiotherapy, cancer

Brief summary

The purpose of this study is to determine whether specific assays of DNA damage repair proteins can be used in patients undergoing radiation therapy. The ultimate goal of this research is to develop clinically useful biomarkers from blood samples that could be used to customize radiation treatment for individuals, leading to reduced side effects and improved outcomes.

Interventions

None listed

Sponsors

Virginia Mason Hospital/Medical Center
CollaboratorOTHER
Fred Hutchinson Cancer Center
CollaboratorOTHER
Benaroya Research Institute
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* patients \> 18 years of age with primary lung, esophageal or rectal cancer receiving neo-adjuvant chemoradiotherapy before planned resection * patients with clinically localized prostate cancer receiving definitive radiation therapy with external beam treatment. brachytherapy as a boost and/or hormonal therapy are allowed. * patients with head and neck, lung, esophageal or cervical cancer who will receive definitive radiotherapy

Exclusion criteria

* prior history of chemotherapy given within 6 months before enrollment. * prior radiotherapy or radionuclide treatment and/or brachytherapy within 6 months prior to enrollment. * unwillingness to comply with tests, protocol, or informed consent. * concurrent enrollment on any protocol that would require non-compliance with treatment procedures. * chemotherapy required within 2 hours following first dose of XRT. * PET scan done within 48 hours of first blood draw. * nuclear medicine exposure within 4 days prior to first draw.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026