Return to List

Study Summary
No. ID03-0111:.......Bladder......Arlene Siefker-Radtke......Genitourinary Medical Oncology
.
Study Summary Title
Study Summary
Number:
ID03-0111
Study Title:Phase II Trial of 5-FU, Leucovorin, Gemcitabine, and Cisplatin for Adenocarcinomas of the Urothelial Tract and Urachal Remnant
.
Physician New Patient Referral
Name:Arlene Siefker-RadtkePatients Call:800-392-1611 (in U.S.A.) 713-792-6161 (outside U.S.A.)
Dept:Genitourinary Medical OncologyReferring MD
Call:
800-392-1611 (in U.S.A.) 713-792-6161 (outside U.S.A.)
Phone:713-792-2830
Contact us about clinical trials
.
General Information
Disease Group:BladderSupported By:N/A
Phase of Study:Phase IIReturn
Visit:
Every 2 cycles (6 weeks)
Treatment
Agents:
5-Fluorouracil
Cisplatin
Gemcitabine
Leucovorin
Home Care:Chemotherapy may be given at home.
Treatment Loc:Only at MDACC
Estimated
Length of Stay
in Houston:
4-5 days every 3 weeks to receive chemotherapy.
Description/
Intervention:
The goal of this clinical research study is to learn if treatment with a
combination of 4 chemotherapy drugs can help to shrink or slow the growth of
adenocarcinoma. The drugs used in the combination chemotherapy are:
5-fluorouracil (5FU), leucovorin, gemcitabine, and cisplatin.
.
Study Objectives / Outcomes
To estimate the response rate and overall survival of patients with metastatic or unresectable adenocarcinomas of the urothelial tract or urachal remnant who are treated with combination chemotherapy consisting of 5-FU, leucovorin, gemcitabine and cisplatin.
.
Study Status Information
Study Activation / Registration Date:04/23/2003
IRB Review and Approval Date:04/16/2003
Study Type:Therapeutic
Recruitment Status:Closed
Projected Accrual:N/A
.
Enrollment Eligibility
If you do not meet the enrollment eligibility, there may be other treatment options for you. Please Contact the Referral Office for more information.

Inclusion Criteria:1) Histologic proof of cancer originating from the urinary tract with adenocarcinoma as the predominant (>/= 50%) histology. Dr. Czerniak and/or Dr. Tamboli will be consulted in equivocal cases of mixed histology. The Study Chairman is the final arbiter in questions of mixed histology.

2) Bi-dimensionally measurable disease. All patients must have measurable or evaluable disease. In general, liver and lung lesions should be at least 1 cm, and patients with node-only disease should have lesions of >/= 1.5 cm in greatest dimension. Patients with disease confined to bone may be eligible if a measurable lytic defect, or soft-tissue component in present. Those without measurable disease may be eligible if a serum marker is elevated (>/= 4 x ULN) (ie: CEA, CA-125, CA19-9, bhCG, etc).

3) (# 2 cont'd) The Study Chairman is the final arbiter in questions related to measurability. Patients with a three-dimensional mass or pelvic sidewall fixation on bladder examination under anesthesia are considered to have measurable disease.

4) Patients are eligible if they have evidence of metastatic disease, or if their tumor is surgically unresectable. In the absence of grossly metastatic disease, all patients should be seen and evaluated by a member of the Urology staff to assess their potential for resection.

5) Patients must have adequate physiologic reserves as evidenced by: • Life expectancy of at least 9 months (based on co-morbidity) & at least 9 weeks based on the natural history of their cancer. • Zubrod Performance Status (PS) of </= 2; or 3 if of recent onset and due entirely to the cancer and not to cormorbidity, and especially if the compromised performance status is due to uncontrolled pain which is expected to be rapidly reversible when therapy starts.

6) (#5 cont'd) • Adequate bone marrow function as defined by absolute neutrophil count >/= 1,800 and platelet count >/= 150,000. Supranormal values judged to be of benign or inconsequential etiology are acceptable. • Transaminase (either SGPT or SGOT) </= 2x the upper limit of normal. • Conjugated bilirubin </= 2x the upper limit of normal. • Creatinine clearance (either measured or estimated using the formula of Cockcroft and Gault) of >/= 35 mL/min: CLcr = [(140-age) • wt(kg)]/[72 •Creat (mg/dL)] (For females, x 0.85)

7) Patients must sign an informed consent indicating that they are aware of the investigational nature of this study, in keeping with the policies of this hospital.

8) Patients must be at least 6 weeks out from pelvic irradiation, and must not have had more than 10% of the bone marrow irradiated.

9) Patients with a history of cardiac disease, or evidence of ischemic heart disease on EKG must have adequate cardiac function with an EF >/= 40% to participate.

10) Patient must be at least 18 years of age to participate in this study.

Exclusion Criteria:1) Patients with metastases to the bladder from a primary adenocarcinoma arising outside the urinary tract are ineligible.

2) Overt psychosis or mental disability or otherwise incompetent to give informed consent.

3) A life threatening illness (unrelated to tumor) that would prevent completion of protocol therapy.

4) Pregnant or nursing women, as the drug therapy regimen, and support medications pose significant potential risks to the fetus and newborn.

5) Patients with second malignancies are eligible provided that the expected outcome from the second cancer is such that this will not interfere in the delivery of this therapy, or the assessment of response.

6) Patients with uncontrolled CNS metastases are not eligible.

.
Links
Registration Number: NCT00082706
Study Information on Clinical Trials Registry (clinicaltrials.gov)

Other Links:
.
Results


Return to Clinical Trials at M.D. Anderson Cancer Center