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Clinical Trials/ISRCTN57274668
ISRCTN57274668
Completed
未知

Renal cancer biomarkers of angiogenesis in renal cell carcinoma (RCC): a multicentre, prospective, non-randomised, observational study

Cambridge University Hospitals NHS Foundation Trust0 sites80 target enrollmentFebruary 7, 2011

Overview

Phase
未知
Intervention
Not specified
Conditions
Renal cell carcinoma
Sponsor
Cambridge University Hospitals NHS Foundation Trust
Enrollment
80
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
February 7, 2011
End Date
January 31, 2012
Last Updated
4 years ago
Study Type
Observational
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\. Newly diagnosed histologically or cytologically confirmed renal cell carcinoma with a clear cell component; patients who have a radiological diagnosis of probable renal cell carcinoma can be included whilst still awaiting biopsy or surgery and once confirmed to have clear cell renal cell carcinoma, they will be included in the study. If their histology confirms a non\-clear cell renal cell carcinoma, they will be replaced.
  • 2\. Metastatic renal cell carcinoma with a clear cell component with previous nephrectomy but with no previous history of use of systemic therapy with the exception of immunotherapy, provera and bisphosphonates. Prior palliative radiotherapy is permitted.
  • 3\. Ability and willingness to provide written informed consent
  • 4\. Ability and willingness to co\-operate with study procedures, including blood and urine sampling
  • 5\. Aged greater than or equal to 18 years, either sex

Exclusion Criteria

  • 1\. Previous history of cancer other than RCC, autoimmune diseases or known active infection
  • 2\. Previous history of use of systemic therapy for treatment of renal cell carcinoma other than immunotherapy, provera and bisphosphonates. Prior palliative radiotherapy is not an exclusion criterion.
  • 3\. Patients who commence therapy in between study visits (sample collection); although if the first sample is already collected before starting treatment, then that sample will be processed and the second sample will not be collected
  • 4\. Known human immunodeficiency virus (HIV) or acquired immunodeficiency syndrome (AIDS)\-related illness, HBV and HCV

Outcomes

Primary Outcomes

Not specified

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