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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00900536
Other study ID # MRC-RE05-TRANSORCE
Secondary ID CDR0000601175EU-
Status Completed
Phase N/A
First received May 9, 2009
Last updated August 9, 2013
Start date July 2007
Est. completion date June 2012

Study information

Verified date November 2008
Source National Cancer Institute (NCI)
Contact n/a
Is FDA regulated No
Health authority Unspecified
Study type Observational

Clinical Trial Summary

RATIONALE: Studying samples of blood and/or tissue in the laboratory from patients with kidney cancer receiving sorafenib may help doctors learn more about changes that occur in DNA and identify biomarkers related to cancer. It may also help doctors predict how well patients will respond to sorafenib.

PURPOSE: This research study is looking at the DNA in blood and/or tissue samples from patients with primary kidney cancer receiving sorafenib on clinical trial MRC-RE05-SORCE.


Description:

OBJECTIVES:

- Examine the relationship between tumor genotype, expression, and patient outcome.

- Examine the relationship between constitutional genotype and patient outcome.

OUTLINE: This is a multicenter study.

Patients undergo blood and/or tissue sample collection for laboratory studies. Laboratory studies include generation of tissue microarrays; analysis of protein expression by immunohistochemistry; tumor DNA extraction and whole genome amplification; detection of VHL or other relevant gene mutations by direct sequencing; and constitutional (lymphocyte DNA) genotyping by single nucleotide polymorphism analysis.


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date June 2012
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility DISEASE CHARACTERISTICS:

- Histologically confirmed resected renal cell carcinoma

- Clear cell or non-clear cell tumor

- Receiving sorafenib tosylate on clinical trial MRC-RE05-SORCE

PATIENT CHARACTERISTICS:

- Not specified

PRIOR CONCURRENT THERAPY:

- See Disease Characteristics

Study Design

N/A


Related Conditions & MeSH terms


Intervention

Genetic:
mutation analysis

polymorphism analysis

protein expression analysis

Other:
immunohistochemistry staining method

laboratory biomarker analysis


Locations

Country Name City State
United Kingdom Addenbrooke's Hospital Cambridge England

Sponsors (1)

Lead Sponsor Collaborator
Medical Research Council

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Relationship between tumor genotype, expression, and patient outcome No
Primary Relationship between constitutional genotype and patient outcome No
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