Erlotinib and Green Tea Extract (Polyphenon® E) in Preventing Cancer Recurrence in Former Smokers Who Have Undergone Surgery for Bladder Cancer

Completed · Phase 2 · Has a placebo group

Conditions studied: Bladder Cancer

In brief

RATIONALE: Erlotinib may stop the growth of tumor cells by blocking the enzymes necessary for their growth. Green tea extract (Polyphenon® E) contains certain ingredients that may slow the growth of tumor cells and prevent the recurrence of cancer. Giving erlotinib or green tea extract after surgery may kill any remaining tumor cells and may prevent the recurrence of bladder cancer. PURPOSE: This randomized phase II trial is studying how well giving erlotinib together with green tea extract works in preventing cancer recurrence in former smokers who have undergone surgery for bladder cancer.

Key facts

Study ID

NCT00088946

Run by

Jonsson Comprehensive Cancer Center

People needed

17

Starts

2004-05-01

Expected to finish

2006-07-01

Last updated by the study team

2020-07-31

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Participants must be former smokers and have ceased smoking at study entry.
• Participants with any previous history of prior cancer diagnosis of Grade 1, 2, or 3, Ta or T1 papillary TCC, or CIS TCC, histologically confirmed, with a newly diagnosed or recurrent tumor within 6 months of accrual who are rendered disease free by standard of care. Patients with Grade 1 papillary tumors must meet at least one of the following additional criteria:
• multiple, synchronous tumors (>2)
• a single tumor greater than 1 cm in size
• At study entry, patients must have no evidence of disease
• Participants may have been previously treated with intravesical therapy.
• Age>18 years
• Transurethral resection of bladder tumor within 6 months prior to entry on to study
• Participants must have a signed written informed consent
• Agreement with complete abstinence from heterosexual intercourse or with the use of contraception during the treatment phase in women of childbearing potential
• Negative pregnancy test in women of childbearing potential
• Patients must have adequate bone marrow function at study entry (WBC>3000, platelets>100000/mm3, and hemoglobin>10g/dl)
• Patients must have satisfactory renal and hepatic function, defined as plasma creatinine of < 1.5mg/dl, total bilirubin < 1.5, and AST/ALT < 1.5 x the upper limit of normal
• Patients with evidence of obstructive lung disease as the etiology of a low diffusing capacity will still be eligible as long as the chest radiograph does not demonstrate interstitial changes

You may not qualify if…

• Prior chemotherapy or radiotherapy
• Prior (within 2 years) or concurrent malignancies, except non-melanomatous skin tumors or carcinoma in situ of the cervix
• Significant medical or psychiatric condition that would make the participant a poor protocol candidate
• TCC greater than or equal to T2 at most recent diagnosis
• Involvement of the upper urinary tract prior to or at the time of initial tumor resection
• Prior treatment with experimental drugs, high dose steroids, or with any other cancer treatment within 4 weeks prior to the first dose of study drug and for the duration of the study
• Positive pregnancy test at any time throughout the course of the study
• Normal consumption of greater than 5 cups of green tea daily
• Participants taking a known CYP 3A4 inducer or food products and medications known to be inhibitors or metabolized by CYP3A4/5 such as erythromycin, ketoconazole, etc. will be excluded since these drugs may be expected to result in altered exposure of Erlotinib
• ECOG performance status > 1
• History of idiopathic pulmonary fibrosis or other interstitial lung disease
• Use of tricyclic antidepressants, including imipramine, dothiepin, and mianserin
• Use within the last 12 months of amiodarone, methotrexate, isoniazid, minocycline, or nitrofurantoin
• History of environmental or occupational metal dust or wood dust exposure
• History of connective tissue disease, including scleroderma, rheumatoid arthritis, Sjogren's Syndrome, or sarcoid
• Significant ophthalmologic abnormalities or patients using contact lenses
• Evidence of interstitial lung disease on chest radiograph
• Patients without obvious interstitial lung disease on chest radiograph will be excluded if they have evidence of parenchymal restrictive lung disease on pulmonary function testing as identified by the following criteria:
• Both vital capacity and total lung capacity <80% of predicted value
• A diffusing capacity of the lung for carbon monoxide, corrected for hemoglobin, < 75% of predicted value

Where it is running

• Bladder Cancer Genitourinary Oncology, PC — Phoenix, Arizona, United States
• Veterans Affairs Medical Center - West Los Angeles — Los Angeles, California, United States
• Jonsson Comprehensive Cancer Center at UCLA — Los Angeles, California, United States
• Santa Monica UCLA Medical Center — Santa Monica, California, United States
• Mayo Clinic Cancer Center — Rochester, Minnesota, United States

Full record on ClinicalTrials.gov

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