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Status:

TERMINATED

BCG With or Without Gefitinib in Treating Patients With High-Risk Bladder Cancer

Lead Sponsor:

NCIC Clinical Trials Group

Conditions:

Bladder Cancer

Eligibility:

All Genders

18-120 years

Phase:

PHASE3

Brief Summary

RATIONALE: Biological therapies, such as BCG, may stimulate the immune system in different ways and stop tumor cells from growing. Gefitinib may stop the growth of tumor cells by blocking some of the ...

Detailed Description

OBJECTIVES: Primary * Compare the impact of gefitinib and intravesical BCG vs intravesical BCG alone on time to treatment failure in patients with high-risk, superficial transitional cell carcinoma ...

Eligibility Criteria

Inclusion

  • DISEASE CHARACTERISTICS:
  • Histologically confirmed transitional cell carcinoma (TCC) of the bladder meeting ≥ 1 of the following criteria:
  • Noninvasive papillary carcinoma (Ta) with ≥ 1 of the following characteristics:
  • Recurrence of bladder tumor(s) ≥ grade 2 within 6 months after transurethral resection (TUR)
  • Three or more bladder tumors ≥ grade 2 at the time of TUR
  • Bladder tumor(s) ≥ 5 cm in size and ≥ grade 2 at the time of TUR
  • Any grade 3 bladder tumor(s)
  • Carcinoma in situ (Tis)
  • At least grade 2 tumor that invades the subepithelial connective tissue (T1)
  • Has undergone TUR of all visible bladder lesions within the past 21 to 60 days with biopsy of the underlying bladder wall for all tumors and cold-cup biopsy of all suspicious areas
  • No metastatic disease as confirmed by negative radiology within the past 16 weeks, including the following:
  • Chest x-ray
  • Imaging of the upper urinary tract by 1 of the following methods:
  • CT scan, MRI, or ultrasound of the abdomen and pelvis
  • Intravenous pyelogram
  • Retrograde pyelogram
  • No evidence of TCC of the upper urinary tract
  • No mixed histology of bladder cancer (i.e., TCC and squamous cell carcinoma of the bladder or TCC and small cell carcinoma of the bladder) at the most recent TUR
  • PATIENT CHARACTERISTICS:
  • ECOG performance status 0-2
  • Life expectancy \> 5 years
  • Negative routine urine microscopy and negative urine culture within the past 14 days
  • Willing to complete quality of life questionnaires in English or French
  • Inability to complete questionnaires due to illiteracy in English or French, loss of sight, or other reason allowed
  • WBC ≥ 3,000/mm³
  • Absolute neutrophil count ≥ 1,500/mm³
  • Platelet count ≥ 100,000/mm³
  • Bilirubin ≤ 1.5 times upper limit of normal (ULN)
  • AST and ALT ≤ 1.5 times ULN
  • Alkaline phosphatase ≤ 1.5 times ULN
  • Creatinine ≤ 1.5 times ULN
  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile patients must use effective contraception during and for 3 months after study completion
  • No significant history of cardiac disease including, but not limited to, any of the following:
  • Uncontrolled high blood pressure
  • Unstable angina
  • Congestive heart failure
  • Myocardial infarction within the past year
  • Cardiac ventricular arrhythmias requiring medication
  • No active urinary tract infection
  • No active infection, including tuberculosis
  • No serious underlying medical conditions that would impair the ability of the patient to receive protocol treatment
  • No febrile illness or gross hematuria
  • No impaired immune response from any cause (congenital, therapy, or disease)
  • No clinically significant or untreated ophthalmologic condition (e.g., Sjögren's syndrome)
  • No gastrointestinal conditions (e.g., Crohn's disease or ulcerative colitis)
  • No history of psychiatric or neurological disorder that would limit study compliance
  • No other malignancies except for adequately treated nonmelanoma skin cancer, curatively treated in situ cancer of the cervix, or other solid tumors curatively treated with no evidence of disease for ≥ 5 years
  • No contraindications to spinal or general anesthesia as required for a TUR
  • No known hypersensitivity to BCG or gefitinib
  • No history of allergic reactions attributed to compounds of similar chemical or biologic composition to the study drugs
  • PRIOR CONCURRENT THERAPY:
  • See Disease Characteristics
  • More than 12 months since prior intravesical immunotherapy (including BCG +/- interferon)
  • More than 6 months since prior intravesical chemotherapy (including mitomycin C, thiotepa, doxorubicin hydrochloride)
  • Single dose of intravesical mitomycin C at the time of the most recent TUR (within the past 21 to 60 days) allowed if considered standard care
  • No other prior or concurrent immune modulator therapy
  • No prior pelvic radiation
  • No prior gefitinib
  • No other concurrent experimental anticancer drugs
  • No concurrent use of drugs that induce CYP3A4 enzymes that have been shown to significantly reduce plasma concentrations of gefitinib (including phenytoin, carbamazepine, barbiturates, rifampin, or Hypericum perforatum \[St. John's wort\])
  • No concurrent grapefruit juice

Exclusion

    Key Trial Info

    Start Date :

    January 4 2007

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ACTUAL

    End Date :

    January 6 2012

    Estimated Enrollment :

    41 Patients enrolled

    Trial Details

    Trial ID

    NCT00352079

    Start Date

    January 4 2007

    End Date

    January 6 2012

    Last Update

    August 4 2023

    Active Locations (6)

    Enter a location and click search to find clinical trials sorted by distance.

    Page 1 of 2 (6 locations)

    1

    Clinical Research Unit at Vancouver Coastal

    Vancouver, British Columbia, Canada, V5Z 1M9

    2

    Hamilton and District Urology Association

    Hamilton, Ontario, Canada, L8N 4A6

    3

    London Regional Cancer Program

    London, Ontario, Canada, N6A 4L6

    4

    Univ. Health Network-Princess Margaret Hospital

    Toronto, Ontario, Canada, M5G 2M9