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Clinical Trials/NCT00645593
NCT00645593
Completed
Phase 2

Phase II Randomized Trial of Gemcitabine and Cisplatin With or Without Cetuximab in Patients With Urothelial Carcinoma

University of Michigan Rogel Cancer Center14 sites in 1 country89 target enrollmentMarch 2008

Overview

Phase
Phase 2
Intervention
Gemcitabine,
Conditions
Bladder Cancer
Sponsor
University of Michigan Rogel Cancer Center
Enrollment
89
Locations
14
Primary Endpoint
Percentage of Participants That Respond to Treatment in Arm 1 and Arm 2
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

This study will compare the effects, good and/or bad, of chemotherapy (Gemcitabine and Cisplatin) with or without the addition of the chemotherapy drug Cetuximab to find out which treatment is better.

Detailed Description

Urothelial cancer typically begins in the lining of the bladder, the balloon-shaped organ in the pelvic area that stores urine. Urothelial cancer can also begin in the ureter (the tube connecting the kidney and bladder), part of the kidney itself, or the urethra (the tube you pass urine out of). Some Urothelial cancers remain confined to the lining, while in other cases they spread to other areas. Treatment for these cancers varies greatly depending on the stage of disease at the time of diagnosis. Study participants in this research study will have a diagnosis of urothelial cancer that is advanced or has come back after prior therapy. There are two standard chemotherapeutic regimens for the management of this disease. One is the combination of the drugs, methotrexate, vinblastine, doxorubicin, and cisplatin (MVAC). However the toxicities associated with this treatment regimen (side effects) is high. The other is a combination of two drugs called Cisplatin and Gemcitabine. These drugs are also known to destroy urothelial cancer cells, and are better tolerated by patients. All study participants will receive both of these drugs. Another anti-cancer drug called Cetuximab is known to delay or prevent tumor growth and in some cases to lead to death of cancer cells by blocking certain cellular pathways that lead to tumor development. This drug has been approved by the United States Food and Drug Administration (FDA) for the treatment of colorectal cancer and for treatment of head and neck cancers. The use of Cetuximab for the treatment of urothelial cancer is investigational in this study. The purpose of this study is to compare the safety and efficacy of Gemcitabine and Cisplatin administered with or without the addition of Cetuximab in study participants with urothelial cancer. This is a randomized research study. Study participants will be randomized to receive either gemcitabine and cisplatin alone or in combination with Cetuximab.

Registry
clinicaltrials.gov
Start Date
March 2008
End Date
June 2015
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Study participants will be male or female at least 18 years of age
  • Study participants will have a histologic/cytologic diagnosis of urothelial carcinoma (transitional cell carcinoma; either pure or mixed histology) that is metastatic, locally recurrent, or unresectable (T4bN0 or any T, N2030)
  • Study participants must have measurable disease by radiologic imaging. Study participants that have received previous radiation therapy, recovered from side effects and have not had more than 25% of the bone marrow
  • Study participants must have adequate bone marrow function

Exclusion Criteria

  • Study participants may not have received previous systemic chemotherapy for the current stage of disease with the following exception: prior neoadjuvant or adjuvant chemotherapy is allowed provided it has been at least 6 months since treatment with non-cisplatin containing regimens and \> 1 year since treatment with a cisplatin containing regimen
  • Study participants may not have received prior therapy targeting the EGFR pathway
  • Study participants may not have a history or known spinal cord compression, or carcinomatous meningitis, or evidence of symptomatic brain or leptomeningeal disease on screening CT or MRI scan
  • Study participants may not have known HIV due to the intense nature of the chemotherapy in this trial
  • Study subjects may not have a history of congestive heart failure (CHF), chronic renal failure, active TIAs, recent (in the last 6 months) stroke, symptomatic pulmonary embolism (PE), or myocardial infarction.
  • Study participants with history of DVT or incidental or asymptomatic PE will be eligible for the study as deemed appropriate by the treating physician provided they continue prophylactic or full dose anticoagulation as per standards of care for the specific event.
  • Study participants must not have a prior grade 3 or 4 severe infusion reaction to monoclonal antibodies
  • Study participants may not be pregnant or breastfeeding
  • Study participants may not receive concurrent treatment on another therapeutic clinical trial.

Arms & Interventions

Arm 1, Gemcitabine and Cisplatin

Gemcitabine and Cisplatin, as described in the intervention

Intervention: Gemcitabine,

Arm 1, Gemcitabine and Cisplatin

Gemcitabine and Cisplatin, as described in the intervention

Intervention: Cisplatin

Arm 2, Cetuximab, Gemcitabine and Cisplatin

Gemcitabine and Cisplatin with Cetuximab, as described in the intervention

Intervention: Gemcitabine,

Arm 2, Cetuximab, Gemcitabine and Cisplatin

Gemcitabine and Cisplatin with Cetuximab, as described in the intervention

Intervention: Cisplatin

Arm 2, Cetuximab, Gemcitabine and Cisplatin

Gemcitabine and Cisplatin with Cetuximab, as described in the intervention

Intervention: Cetuximab

Outcomes

Primary Outcomes

Percentage of Participants That Respond to Treatment in Arm 1 and Arm 2

Time Frame: 3 years

The primary objective is to compare the overall response rate of participants with locally advanced or metastatic urothelial carcinoma treated with gemcitabine and cisplatin with or without cetuximab. Overall response rate is defined as the percentage of participants that experience Complete Response (CR) (Disappearance of all target lesions) or Partial Response (PR) (\>=30% decrease in the sum of the longest diameter of target lesions).

Secondary Outcomes

  • The Number of Grade 3 to 5 Adverse Events Experienced by Arm 1 and Arm 2(3 years)
  • Median Progression-free Survival Time in Months(3 years)
  • Median Overall Survival in Months(3 years)

Study Sites (14)

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