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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00900042
Other study ID # CDR0000502305
Secondary ID SWOG-9023U10CA03
Status Completed
Phase N/A
First received May 9, 2009
Last updated February 21, 2014
Start date July 1993
Est. completion date January 2003

Study information

Verified date February 2014
Source Southwest Oncology Group
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Observational

Clinical Trial Summary

RATIONALE: DNA analysis of tumor tissue may help doctors predict how well patients will respond to treatment.

PURPOSE: This laboratory study is analyzing the DNA in tumor tissue from patients with metastatic kidney cancer.


Description:

OBJECTIVES:

- Determine if cytogenetic abnormalities can predict clinical outcome, in terms of response to treatment and survival, in patients with metastatic renal cell carcinoma registered to the nephrectomy arm (arm I) of SWOG-8949.

- Correlate cytogenetic abnormalities and DNA content analysis (DNA index and S-phase fraction) with clinical outcome.

OUTLINE: This is a partially prospective, partially retrospective, multicenter, companion study.

Paraffin-embedded tumor tissue specimens from patients enrolled in SWOG-8949 are evaluated by cytogenetic analysis (e.g., presence of trisomy and loss of Y chromosome) and flow cytometric analysis (e.g., presence of nondiploid cells and presence of abnormal proliferation index).

PROJECTED ACCRUAL: A total of 80 patients will be accrued for this study.


Recruitment information / eligibility

Status Completed
Enrollment 34
Est. completion date January 2003
Est. primary completion date December 2002
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility DISEASE CHARACTERISTICS:

- Diagnosis of renal cell carcinoma

- Any T, any N, M1 disease as specified in SWOG-8949

- Eligible for and registered on the nephrectomy arm* (arm I) of SWOG-8949 NOTE: *Patients must be registered on this study before undergoing nephrectomy on SWOG-8949

PATIENT CHARACTERISTICS:

- Not specified

PRIOR CONCURRENT THERAPY:

- See Disease Characteristics

Study Design

Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Genetic:
DNA ploidy analysis

DNA stability analysis

chromosomal translocation analysis

cytogenetic analysis

Other:
flow cytometry

laboratory biomarker analysis


Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Southwest Oncology Group National Cancer Institute (NCI)

Outcome

Type Measure Description Time frame Safety issue
Primary Number of successes per number of evaluable samples Success is defined as obtaining at least 10 analyzable metaphases. up to 4 years after registration No
Primary Number of abnormalities per number of successes Abnormality is defined as at lease one clonal chromosomal abnormality. up to 4 years after registration No
Primary Correlation of tumor response to treatment with the type and number of abnormalities Abnormality is defined as at lease one clonal chromosomal abnormality. up to 4 years after registration No
Primary Correlation of time from diagnosis to development of metastatic disease with the type and number of abnormalities Abnormality is defined as at lease one clonal chromosomal abnormality. up to 4 years after registration No
Primary Correlation of time from first diagnosis of metastatic disease until death with the type and number of abnormalities Abnormality is defined as at lease one clonal chromosomal abnormality. up to 4 years after registration No
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