Cisplatin, Gemcitabine and Bevacizumab in Combination for Metastatic Transitional Cell Cancer

NCT ID: NCT00234494

Last Updated: 2016-03-14

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 45 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2005-11-30
• Study Completion Date: 2008-12-31

Brief Summary

Cisplatin is a very important agent for the treatment of TCC as it has a single agent response rate of approximately 15%. However, it has been most important as a part of combination chemotherapy, MVAC initially and now in combination with gemcitabine. Single agent gemcitabine has demonstrated an overall response rate (ORR) of approximately 25%, including some complete responses (CR), with minimal toxicity in patients with advanced bladder cancer. Bevacizumab, a murine anti-human VEGF monoclonal antibody, has been advanced for use in combination with cytotoxic chemotherapy to delay time to disease progression in patients with metastatic solid tumors.

This trial is designed to further assess the efficacy, safety and tolerability of this regimen in this patient population.

Detailed Description

OUTLINE: This is a multi-center study.

• Cisplatin 70 mg/m2 Day 1
• Gemcitabine 1250 mg/m2 Day 1 and 8
• Bevacizumab 15 mg/kg Day 1

Review toxicity every cycle (every 3 weeks) Review for radiographic response every 2 cycles (every six weeks)

Progressive disease = off protocol therapy

Patients will be treated for up to a maximum of 8 cycles of cisplatin and gemcitabine (24 weeks of therapy). If a patient has not progressed by the end of 24 weeks (completion of cisplatin and gemcitabine), then patient will be treated with bevacizumab at 15 mg/kg every three weeks for a maximum of 12 months of bevacizumab therapy (since study entry).

If at any time patient has undue toxicity or progressive disease, patient will be removed from the study and followed until progression and for survival.

If the patient has Grade 3 or 4 neurotoxicity and/or the creatinine rises above 2.0, then the cisplatin will be discontinued and the patient continued on study and treated with gemcitabine and bevacizumab at the same dose and schedule.

ECOG Performance Status 0 or 1

Hematopoietic:

• White blood cell count > 3000/mm3
• Absolute neutrophil count (ANC) > 1500 mm/3
• Platelet count > 100,000/mm3
• Hemoglobin > 8 g/dL (may be transfused or receive erythropoietin support to maintain or exceed this level).
• INR < 1.5
• No full dose/therapeutic anticoagulation with either low molecular weight heparin or unfractionated heparin or coumadin

Hepatic:

• Total bilirubin of <1.5 mg/dL
• ALT <5 times upper limit of normal for subjects with documented liver metastases; <2.5 times the upper limit of normal for subjects without evidence of liver metastases.

Renal:

• Serum creatinine of < 1.5 mg/dL.
• Urine protein:creatinine ratio < 1.0 at screening

Cardiovascular:

• No history of myocardial infarction or stroke within the last 6 months
• No uncontrolled hypertension (blood pressure of >160 systolic and/or 110 diastolic mmHg on medication)
• No unstable angina, New York Heart Association (NYHA) Grade II or greater congestive heart failure
• No unstable symptomatic arrhythmia requiring medication (subjects with chronic atrial arrhythmia, i.e., atrial fibrillation or paroxysmal supraventricular tachycardia are eligible), or clinically significant peripheral vascular disease.

Pulmonary:

• Not specified

Conditions

Bladder Cancer

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Single Group Assignment

Cisplatin + Gemcitabine + Bevacizumab

Group Type: EXPERIMENTAL

Cisplatin

Intervention Type: DRUG

Cisplatin 70 mg/m2, day 1

Gemcitabine

Intervention Type: DRUG

Gemcitabine 1250 mg/m2, day 1 and 8

Bevacizumab

Intervention Type: DRUG

Bevacizumab 15mg/kg, day 1

Interventions

Cisplatin

Cisplatin 70 mg/m2, day 1

Intervention Type: DRUG

Gemcitabine

Gemcitabine 1250 mg/m2, day 1 and 8

Intervention Type: DRUG

Bevacizumab

Bevacizumab 15mg/kg, day 1

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Previously untreated or relapsed locally advanced or metastatic transitional cell carcinoma of the bladder. (Patients with pathology showing ANY component of non-transitional cell histology are not eligible).
• Relapsed patients may have received prior chemotherapy ≥ one year prior to study registration as part of a neoadjuvant or adjuvant regimen and must not have had intervening therapy from the end of that treatment until study entry.
• Measurable disease as per RECIST.
• Prior radiation therapy, immunotherapy, cytokine, biologic or vaccine therapy must be greater than 28 days prior to being registered for protocol therapy,

Exclusion Criteria

• No known central nervous system metastasis. (imaging of brain only required if clinically indicated)
• No prior organ allograft.
• No history of other disease, metabolic dysfunction, physical examination finding, or clinical laboratory finding giving reasonable suspicion of a disease or condition that contraindicates the use of an investigational drug or that might affect the interpretation of the results of the study or render the subject at high risk from treatment complications.
• No evidence of bleeding diathesis or coagulopathy.
• No history of serious, non-healing wound, ulcer or bone fracture
• No history of abdominal fistula, gastrointestinal perforation, or intra-abdominal abscess within 6 months prior to being registered for protocol therapy.
• No prior history of malignancy in the past 5 years with the exception of basal cell and squamous cell carcinoma of the skin. Other cancers with low potential for metastasis, such as in situ cancers (e.g., Grade 1, TA TCC (low grade superficial bladder cancer), colonic polyp with focus of adenocarcinoma) can also be enrolled after approval from the study chair.
• No major surgical procedure, open biopsy, or significant traumatic injury less than 28 days prior to being registered for protocol therapy.
• Patients are not eligible if the need for any major surgical procedure is anticipated during the course of the study.
• Any minor surgical procedures, fine needle aspirations or core biopsies must be greater than 7 days prior to being registered for protocol therapy except procedures to secure a vascular access device which must be greater than 7 days prior to the start of protocol therapy.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Genentech, Inc.

INDUSTRY

Sponsor Role: collaborator

Eli Lilly and Company

INDUSTRY

Sponsor Role: collaborator

Walther Cancer Institute

OTHER

Sponsor Role: collaborator

Hoosier Cancer Research Network

OTHER

Sponsor Role: collaborator

Christopher Sweeney, MBBS

OTHER

Sponsor Role: lead

Responsible Party

Christopher Sweeney, MBBS

Sponsor-Investigator

Responsibility Role: SPONSOR_INVESTIGATOR

Principal Investigators

Christopher Sweeney, M.B.B.S.

Role: STUDY_CHAIR

Hoosier Oncology Group, LLC

Locations

University of Chicago

Chicago, Illinois, United States

Medical & Surgical Specialists, LLC

Galesburg, Illinois, United States

Oncology Hematology Associates of SW Indiana

Evansville, Indiana, United States

Fort Wayne Oncology & Hematology, Inc

Fort Wayne, Indiana, United States

Indiana University Cancer Center

Indianapolis, Indiana, United States

Quality Cancer Center (MCGOP)

Indianapolis, Indiana, United States

Arnett Cancer Care

Lafayette, Indiana, United States

Northern Indiana Cancer Research Consortium

South Bend, Indiana, United States

AP&S Clinic

Terre Haute, Indiana, United States

Siteman Cancer Center

St Louis, Missouri, United States

Oncology Hematology Care, Inc.

Cincinnati, Ohio, United States

Countries

United States

References

Hahn NM, Stadler WM, Zon RT, Waterhouse D, Picus J, Nattam S, Johnson CS, Perkins SM, Waddell MJ, Sweeney CJ; Hoosier Oncology Group. Phase II trial of cisplatin, gemcitabine, and bevacizumab as first-line therapy for metastatic urothelial carcinoma: Hoosier Oncology Group GU 04-75. J Clin Oncol. 2011 Apr 20;29(12):1525-30. doi: 10.1200/JCO.2010.31.6067. Epub 2011 Mar 21.

Reference Type: RESULT

PMID: 21422406 (View on PubMed)

Related Links

http://www.hoosiercancer.org

Hoosier Cancer Research Network Homepage

Other Identifiers

HOG GU04-75

Identifier Type: -

Identifier Source: org_study_id