Status:

COMPLETED

Genetic Determinants of Response to Neoadjuvant Cisplatin-based Chemotherapy in Urothelial Cancer

Lead Sponsor:

University of Chicago

Conditions:

Urothelial Cancer

Eligibility:

All Genders

18-89 years

Brief Summary

This is observational clinical trial to study adult urothelial cancer patients treated with cisplatin-based neoadjuvant chemotherapy. Hypothesis: Identification of genetic and molecular "cisplatin su...

Detailed Description

In this trial patients will submit germline (blood) and tumor tissue samples as part of two existing sample collection protocols for analysis of genetic and molecular markers governing response to che...

Eligibility Criteria

Inclusion

  • Patients with clinical T2 through T4 urothelial carcinoma of the bladder or upper tract.
  • Patients must be deemed appropriate by the treating physician to require cisplatin-based neoadjuvant chemotherapy for urothelial cancer. Consideration of regional nodal status as part of the decision for appropriateness for neoadjuvant chemotherapy will be left to the treating physician.
  • Patients must be scheduled to proceed to definitive urothelial cancer surgery, including either cystectomy or nephrectomy/ureterectomy, after chemotherapy.
  • Age \>18 years.

Exclusion

  • Patients receiving cisplatin-based chemotherapy for urothelial cancer in the adjuvant setting or for metastatic disease.

Key Trial Info

Start Date :

October 1 2009

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

October 16 2017

Estimated Enrollment :

79 Patients enrolled

Trial Details

Trial ID

NCT01206426

Start Date

October 1 2009

End Date

October 16 2017

Last Update

May 4 2018

Active Locations (1)

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1

University of Chicago

Chicago, Illinois, United States, 60637