History & Overview Annual Report President's Pages Center News Community Affairs
Make a Gift Cycle for Survival Fred's Team Rock & Run on the River Yankees Universe Fund Thomas Blake Sr. Memorial Research Fund Donating Blood & Platelets Volunteering Thrift Shop Park Avenue Potluck Cookbook
Press Releases In the News Information for Journalists News@MSKCC
Manhattan New Jersey Long Island Westchester
Working at Memorial Sloan-Kettering Work Sites College Recruitment About Nursing Job Fairs & Career Days Job Search & Apply Online
Making an Appointment

A Phase II Trial of Gemcitabine, Carboplatin, and Bevacizumab in Chemotherapy-naïve Patients with Advanced/Metastatic Urothelial Carcinoma

[Protocol 06-006]


Full Title :
PHASE II TRIAL OF GEMCITABINE, CARBOPLATIN, AND BEVACIZUMAB IN CHEMOTHERAPY NAIVE PATIENTS WITH ADVANCED/METASTATIC UROTHELIAL CARCINOMA
Purpose :

Gemcitabine and carboplatin are two standard chemotherapy drugs used to treat tumors of the urothelial tract. These drugs do not shrink tumors in all patients, however, and when they do, it is generally for a limited amount of time. Scientists are therefore seeking more effective ways to treat these cancers.

The purpose of this study is to evaluate the effectiveness of adding another anticancer drug, bevacizumab, to the combination of gemcitabine and carboplatin in patients with advanced urothelial cancers. Bevacizumab is used to treat advanced colon cancer, under the name Avastin®. It may prevent the development of the blood vessels that tumors need to grow and spread.

Eligibility :

To be eligible for this study, patients must meet several criteria, including but not limited to the following:

  • Patients must have a confirmed diagnosis of transitional cell carcinoma of the bladder, urethra, ureter, or renal pelvis that cannot be surgically removed or has metastasized.
  • Patients may not be eligible or able to receive cisplatin.
  • Patients may not have had prior chemotherapy.
  • At least 4 weeks must have passed since prior radiation therapy or major surgery and entry into the study.
  • Patients must be age 18 or older.

For more information and to see if you are eligible for this study, please contact Dr. Dana E. Rathkopf at 646-422-4379.

Bookmark and SharePrintEmail This Page